Devices

Device Recall STA

Model / Serial
Lot 061781, June 2008
Product Classification
Hematology and Pathology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide.
Product Description
STA Neoplastine CI Plus (10), (cat. 0667). || 12 x 10 ml. in vitro diagnostic for the determination of prothrombin time (PT).
Manufacturer
Diagnostica Stago, Inc.
1 Event
- Recall of Device Recall STA

Manufacturer

Diagnostica Stago, Inc.

Manufacturer Address
Diagnostica Stago, Inc., 5 Century Dr, Parsippany NJ 07054-4607
Source
USFDA

162 devices with a similar name

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Device Recall Status Assure

Model / Serial
153632
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
11 Panel Dip Card (OPI 300) w/Adult, Item No. 11125AA
Manufacturer
Ameditech Inc

Device Recall Status Assure

Model / Serial
144376
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
11 Panel Card (OPI 300) w/Adult, Item No. 71125AA
Manufacturer
Ameditech Inc

Device Recall StarBurst MRI SemiFlex Electrode Device

Model / Serial
Lot No. 4773676, 4776428 and 4780110
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Distribution to the states of AZ, AR, FL, MI, MN, MO, NY, TX, VA, WA and WI., and to the countries of Hungary and Spain.
Product Description
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No. 700-103909; 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615; and 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615
Manufacturer
Angiodynamics

Device Recall Staple loading unit

Model / Serial
OEM Catalog number TA6035L.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Product Description
Medical Device Exchange - Loading Unit w/ DST Series Technology 60mm - 3.5mm; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number TA6035L; || EXP (repackager), Covidien (OEM) || Implantable Staple
Manufacturer
EXP Pharmaceutical Services Corp

Device Recall STAAR AQ CartridgeFP

Model / Serial
1281706, 1282812
Product Classification
Ophthalmic Devices
Device Class
1
Implanted device?
No
Distribution
US
Product Description
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Manufacturer
Staar Surgical Co.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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