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  • Device 2589
  • Manufacturer 31827
  • Event 2705
  • Implant 0
Access Immunoassay System Technical Update 03.1, Part number 387851, Software version 3.29
  • Model / Serial
    Software version 3.29
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    United States only, nationwide.
  • Product Description
    Access Immunoassay System Technical Update 03.1, Part number 387851, Software version 3.29
  • Manufacturer
    Beckman Coulter Inc
  • 1 Event
    • Recall of Access Immunoassay System Technical Update 03.1, Part number 387851, Software version 3.29
Access Ostase Calibrators
  • Model / Serial
    623207 626000 628294 628296
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US Nationwide Distribution in the states of: UT, MI, MA, LA, IN, NC, CA, TX, NJ, IL, WI, MN, FL, KA, NY, CO, WA, KY, VA, and AL. Affected geographies: Belgium, Canada, China, Czech Republic, France, Germany, Greece, Hong Kong, Hungary, India, Italy, Japan, Mexico, Philippines, Portugal, Romania, Russian Federation, Serbia, Singapore, Slovakia, South Africa, South Korea, Spain, Switzerland, Taiwan.
  • Product Description
    Access Ostase Calibrators, Catalog No. 37305, B83876 || Product Usage: || The Access Ostase Calibrators are intended to calibrate the Access Ostase assay for the quantitative determination of bone alkaline phosphatase (BAP) levels in human serum and plasma using the Access Immunoassay Systems.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Access Ostase Calibrators
Access Ostase QC
  • Model / Serial
    628297 623207 626001
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    US Nationwide Distribution in the states of: UT, MI, MA, LA, IN, NC, CA, TX, NJ, IL, WI, MN, FL, KA, NY, CO, WA, KY, VA, and AL. Affected geographies: Belgium, Canada, China, Czech Republic, France, Germany, Greece, Hong Kong, Hungary, India, Italy, Japan, Mexico, Philippines, Portugal, Romania, Russian Federation, Serbia, Singapore, Slovakia, South Africa, South Korea, Spain, Switzerland, Taiwan.
  • Product Description
    Access Ostase QC, Catalog No. 37309, B83877 || Product Usage: || The Access Ostase QC is intended for monitoring system performance of the Access Ostase assay.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Access Ostase QC
Access Peristaltic Pump
  • Model / Serial
    Pump Part Numbers A62712, A62839, A62840, A62841, and A63124; Instrument Part Numbers: 973100, A30260, and A59102.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution -- United States and Canada.
  • Product Description
    Access Peristaltic Pump component of: UniCel DxI 800 Access Immunoassay Systems, UniCel DxI 600 Access Immunoassay Systems, UniCel DxC 880i SYNCHRON Access Clinical Systems. || Intended to be used with the Access Immunoassay System to remove waste from the system.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Access Peristaltic Pump
Access Power Supply Assembly Sled
  • Model / Serial
    Part Number A48196/6845C; Instrument part numbers 81600 and  81600N
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution and Canada
  • Product Description
    Access Power Supply Assembly Sled || Part Number: A48196/6845C; Component of: Access and Access 2 Immunoassay Systems, SYNCHRON LXi 725 System, and UniCel DxC 600i System, for in vitro diagnostic use.
  • Manufacturer
    Beckman Coulter Inc
  • 1 Event
    • Recall of Access Power Supply Assembly Sled
Access Progesterone Assay, Part number 33550.
  • Model / Serial
    All Lots.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    USA and Canada.
  • Product Description
    Access Progesterone Assay, Part number 33550.
  • Manufacturer
    Beckman Coulter Inc
  • 1 Event
    • Recall of Access Progesterone Assay, Part number 33550.
Access Total BhCG (BhCG) Assay
  • Model / Serial
    All lot numbers
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) and the countries of Algeria, Angola, Antigua and Barbuda, Argentina, Armenia, Australia, Bangladesh, Belgium, Brazil, Bulgaria, Chile, China, Colombia, Congo, Croatia, Czech Republic, Djibouti, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Ghana, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kuwait, Lebanon, Libyan Arab Jamahiriya, Lithuania, Malaysia, Mexico, Moldova, Monaco, Morocco, Myanmar, Namibia, Netherlands, New Zealand, Nigeria, Oman, Pakistan, Panama, Philippines, Poland, Puerto Rico, Qatar, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Swaziland, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Uganda, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Zambia, Zimbabwe.
  • Product Description
    Access Total BhCG (BhCG) Assay Part Number 33500 || The Access Total BhCG assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of total BhCG levels in human serum and plasma using the Access Immunoassay Systems.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Access Total BhCG (BhCG) Assay
Access Total T3 Reagent
  • Model / Serial
    All Lots
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide), Canada, and internationally.
  • Product Description
    Access Total T3 Reagent, PN: 33830 || The Access Total T3 assay is used for the quantitative determination of triiodothyronine (T3) levels in human serum and plasma in the assessment of thyroid function and diagnosis of thyroid disorders when T3 levels are between 0.1 and 8.0 ng/mL.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Access Total T3 Reagent
Access Ultrasensitive Insulin Assay Kit
  • Model / Serial
    Part Number 33410, Lot Numbers: 714362 (Exp dt. 3/31/09), 716129 (Exp dt. 6/30/09), 718258 (Exp dt. 7/31/09), 519096 (Exp dt. 10/31/07), 521487 (Exp dt. 2/28/08), 616274 (Exp dt. 7/31/08), 617890 (Exp dt. 7/31/08), 617891 (Exp dt. 7/31/08) and 620204 (Exp dt. 12/31/08)
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide: including USA and Canada.
  • Product Description
    Access Ultrasensitive Insulin Assay Kit, Part Number 33410. The product is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of insulin levels in human serum and plasma (EDTA) using the Access Immunoassay Systems. Beckman Coulter, Inc., Chaska, MN 55318.
  • Manufacturer
    Beckman Coulter Inc
  • 1 Event
    • Recall of Access Ultrasensitive Insulin Assay Kit
ACCUCHEK
  • Model / Serial
    AccuChek Aviva Combo meter 05075645005 packaged in Accu-Chek Combo Kit mg US/English version, 05458544001 and Accu-Chek Combo Kit mg US/Spanish version, 05504686001.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution.
  • Product Description
    ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of the ACCU-CHEK Aviva Combo System)\ || The ACCU-CHEK Combo System is indicated for the treatment of insulin-requiring diabetes and for the quantitative measurement of glucose in fresh capillary whole blood from the finger.
  • Manufacturer
    Roche Diagnostics Operations, Inc.
  • 1 Event
    • Recall of ACCUCHEK
ACCUCHEK Compact Plus
  • Model / Serial
    5599423160, 5599415160, 5919967160, 5919959160, 5919983160, 5907675001
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution.
  • Product Description
    ACCU-CHEK Compact Plus Test Strips || For use with: ACCU-CHEK Compact Plus Meters; 17 count sample strip || 51 count retail strip; 102 count retail strip; 51 count MedBen strip || 51 count Mail Order strip; Sample Kit 16 per case. || The ACCU-CHEK Compact Plus Test Strips are for use with the ACCU-CHEK Compact Plus Blood Glucose Meter to quantitatively measure glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips or palm.
  • Manufacturer
    Roche Diagnostics Operations, Inc.
  • 1 Event
    • Recall of ACCUCHEK Compact Plus
ACCUCHEK Connect Diabetes Management App
  • Model / Serial
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    There are no US distributors as the affected device is not marketed in the US. The affected device was distributed in Germany, Italy and South Africa. The application has been downloaded total of 644 times (Italy-219, South Africa-24, Germany-401) and there are 113 bolus advice activations.
  • Product Description
    ACCU-CHEK Connect Diabetes Management App; Instruction Manual || Designed to transfer data for diabetes management.
  • Manufacturer
    Roche Diabetes Care, Inc.
  • 1 Event
    • Recall of ACCUCHEK Connect Diabetes Management App
ACCU-CHEK Inform meter; catalog No. 3035123.
  • Model / Serial
    All units with firmware version 2.3 that have the OTE (other test entry) functionality enabled.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    ACCU-CHEK Inform meter; catalog No. 3035123.
  • Manufacturer
    Roche Diagnostics Corp.
  • 1 Event
    • Recall of ACCU-CHEK Inform meter; catalog No. 3035123.
ACCU-CHEK Instant Care Kit; Catalog number 91490.
  • Model / Serial
    All units.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    ACCU-CHEK Instant Care Kit; Catalog number 91490.
  • Manufacturer
    Roche Diagnostics Corp.
  • 1 Event
    • Recall of ACCU-CHEK Instant Care Kit; Catalog number 91490.
ACCU-CHEK Instant Meter; Catalog numbers 914 and 924.
  • Model / Serial
    All units.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    ACCU-CHEK Instant Meter; Catalog numbers 914 and 924.
  • Manufacturer
    Roche Diagnostics Corp.
  • 1 Event
    • Recall of ACCU-CHEK Instant Meter; Catalog numbers 914 and 924.
Accu-Chek Performa Test Strips for Blood Glucose Meters
  • Model / Serial
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Product Description
    in-vitro_medical_device
  • Manufacturer
    Roche Diagnostics
  • 1 Event
    • Recall of Accu-Chek Performa Test Strips for Blood Glucose Meters
AccuData
  • Model / Serial
    All units.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and Guam.
  • Product Description
    Roche brand AccuData GTS/GTS Plus System || Replacement Base/Module; Catalog number 3426050, material number 03426050001.
  • Manufacturer
    Roche Diagnostics Corp.
  • 3 Events
    • Recall of AccuData
    • Recall of AccuData
    • Recall of AccuData
Active Intact PTH
  • Model / Serial
    Lot Numbers: 090013, 090121, and 090372
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including MD, NY, GA, NJ, CA, MI, TX, PA, IA, and IN. Internationally to Austria, Brazil, China, Colombia, Czech Republic, France, Germany, Hong Kong, India, Japan, Mexico, and the Russian Federation
  • Product Description
    Active INTACT PTH, Part Number: DSL-8000 || The DSL-80000 ACTIVE Intact PTH IRMA Kit provides materials for the quantitative measurement of Intact PTH (I-PTH) in serum or plasma. The assay is intended for in vitro diagnostic use.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Active Intact PTH
Active I PTH ELISA
  • Model / Serial
    Lot Numbers: 992751
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including MD, NY, GA, NJ, CA, MI, TX, PA, IA, and IN. Internationally to Austria, Brazil, China, Colombia, Czech Republic, France, Germany, Hong Kong, India, Japan, Mexico, and the Russian Federation
  • Product Description
    Active I-PTH ELISA, Part Number: DSL-10-8000 || The DSL-10-80000 ACTIVE I-PTH Enzyme-Linked Immunosorbent Assay (ELISA) Kit provides materials for the quantitative measurement of I-PTH in serum or plasma. This assay is intended for in vitro diagnostic use as an aid in the diagnosis of hyperparathyroidism.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Active I PTH ELISA
Active Prolactin ELISA
  • Model / Serial
    Lot Number: 890291
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide distribution: USA including states of: FL, GA and NC.
  • Product Description
    Active Prolactin ELISA, 96 Wells, DSL-10-4500 || The DSL-10-4500 Active Prolactin Enzyme-Linked Immunosorbent Assay (ELISA) Kit provides materials for the quantitative measurement of prolactin in human serum. This assay is intended for in vitro diagnostic use in the diagnosis and treatment of disorders of the anterior pituitary gland or of the hypothalamus portion of the brain.
  • Manufacturer
    Beckman Coulter Inc.
  • 1 Event
    • Recall of Active Prolactin ELISA
Advance Microdraw Blood Glucose Monitoring System
  • Model / Serial
    Part Number 411100, Lot Number: 09177A
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide: USA including states of CA, MI, MO, MS, NE, OH and TX.
  • Product Description
    Hypoguard Advance Micro-draw Blood Glucose Monitoring System, Product Number : 411100, For In Vitro Diagnostic Use, Manufactured for ARKRAY USA, Inc., Minneapolis, MN 55439 USA. (Package Contents -Advance Micro-draw Blood Glucose Meter, 10 test Strips, Codeing chip and Control Solution (3mL), Lancing device, 10 Lancets, 3V Lithium Battery, Logbook, User Instruction Manual, Quick Reference Guide)
  • Manufacturer
    ARKRAY USA INC.
  • 1 Event
    • Recall of Advance Microdraw Blood Glucose Monitoring System
ADVIA 1200 Chemistry System
  • Model / Serial
    All ADVIA 1200 Chemistry Systems are involved as well as all existing assay lots for Valproic Acid (VPA), Phenytoin (PHNY), Gentamicin (GENT), Digoxin (DIG), and Theophylline (THEO). ADVIA 1200 Part # 094-A001, VPA Part # B01-4784-01, PHNY Part # B01-4775-01, DIG Part # B01-4769-01, GENT Part # B01-4787-01, THEO Part # B01-4772-01.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Puerto Rico, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Columbia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, Ireland, Israel, Italy, Korea, Malaysia, Mexico, The Netherlands, New Zealand, Norway, Poland, Portugal, Russia, Serbia, Singapore, Slovakia, South Africa, Spain, Saudi Arabia, Sweden, Switzerland, Syria, Taiwan, Turkey, and United Kingdom.
  • Product Description
    ADVIA 1200 Chemistry System, Automated Clinical Chemistry Analyzer - human serum, plasma and urine tests. The following are the measured parameters that are within the scope of this ''field correction'': Affected assay: Valproic Acid. Affecting assays: Digoxin; Phenytoin; Gentamicin; Theophylline.
  • Manufacturer
    Bayer Healthcare, LLC (Diagnostics Division)
  • 1 Event
    • Recall of ADVIA 1200 Chemistry System
ADVIA 1200 System Software: 1) V2.00, 2) V2.01
  • Model / Serial
    Product Codes: 1) 10386841, 2) 10469445
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) and the countries of Sweden, Switzerland, Taiwan, Turkey, United Kingdom, and Vietnam.
  • Product Description
    ADVIA 1200 System Software: 1) V2.00, 2) V2.01. || Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.
  • Manufacturer
    Siemens Healthcare Diagnostics
  • 1 Event
    • Recall of ADVIA 1200 System Software: 1) V2.00, 2) V2.01
ADVIA 1650 Chemistry System
  • Model / Serial
    All ADVIA 1650 Chemistry Systems are involved as well as all existing assay lots for Valproic Acid (VPA), Phenytoin (PHNY), Gentamicin (GENT), Digoxin (DIG), and Theophylline (THEO). ADVIA 1650 Part # 073-A001, VPA Part # B01-4784-01, PHNY Part # B01-4775-01, DIG Part # B01-4769-01, GENT Part # B01-4787-01, THEO Part # B01-4772-01.
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Puerto Rico, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Columbia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, Ireland, Israel, Italy, Korea, Malaysia, Mexico, The Netherlands, New Zealand, Norway, Poland, Portugal, Russia, Serbia, Singapore, Slovakia, South Africa, Spain, Saudi Arabia, Sweden, Switzerland, Syria, Taiwan, Turkey, and United Kingdom.
  • Product Description
    ADVIA 1650 Chemistry System, Automated Clinical Chemistry Analyzer - human serum, plasma and urine tests. The following are the measured parameters that are within the scope of this ''field correction'': Affected assay: Valproic Acid. Affecting assays: Digoxin; Phenytoin; Gentamicin; Theophylline.
  • Manufacturer
    Bayer Healthcare, LLC (Diagnostics Division)
  • 1 Event
    • Recall of ADVIA 1650 Chemistry System
ADVIA 1650 System Software: 1) V4.01, 2) V3.52
  • Model / Serial
    Product Codes: 1) 10318424, 2) 10285281
  • Product Classification
    Clinical Chemistry and Clinical Toxicology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) and the countries of Sweden, Switzerland, Taiwan, Turkey, United Kingdom, and Vietnam.
  • Product Description
    ADVIA 1650 System Software: 1) V4.01, 2) V3.52. || Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.
  • Manufacturer
    Siemens Healthcare Diagnostics
  • 1 Event
    • Recall of ADVIA 1650 System Software: 1) V4.01, 2) V3.52
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