Devices

Device Recall Zimmer

Model / Serial
Lot No: 60651168 and 60726506.
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide: USA including states of Arizona, California, Florida, Georgia, Indiana, Michigan, New York, North Carolina, and Virginia, and countries of Germany and Japan.
Product Description
Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; REF 7712-35-02, Zimmer U.K. Ltd., SN3, 4FP, UK
Manufacturer
Zimmer Inc.
1 Event
- Recall of Device Recall Zimmer

Manufacturer

Zimmer Inc.

Manufacturer Address
Zimmer Inc., 345 E. Main St., Warsaw IN 46580-2304
Source
USFDA

263 devices with a similar name

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Device Recall Zimmer Anatomical Shoulder Glenoid

Model / Serial
Lot 2385941.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Maryland.
Product Description
Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented, sterile; REF 01.04214.370.
Manufacturer
Zimmer Inc.

Device Recall Zimmer

Model / Serial
Lot No: 60646894.
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide: USA including states of Arizona, California, Florida, Georgia, Indiana, Michigan, New York, North Carolina, and Virginia, and countries of Germany and Japan.
Product Description
Zimmer Minimally Invasive Solutions Technology, Offset Rasp Handle, Left, 45 degrees, non-sterile; REF/Catalog #: 7712-35-01, Zimmer U.K. Ltd., SN3, 4FP, UK
Manufacturer
Zimmer Inc.

Device Recall Zimmer Hemovac Wound Drainage Device Infection Control Kits

Model / Serial
Lot Numbers: 60009294, 60075254, 60101562, 60156041, 60215686, 60271994, 60314032, 60389073, 60440024, 60506573 and 60590575.
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide-USA, Australia, Canada, Colombia, Denmark, Dubai, Italy, Japan, Mexico and Singapore.
Product Description
Zimmer Hemovac Wound Drainage Device Infection Control Kits, Catalog Number/REF: 00-2550-001-10, 400 ml INF. Cntrl. Kit w/ 3/32" drain, 2.4 mm, 7Fr, PVC, 107 cm, small, sterile, latex free, Rx only; Sold in packages of 10, which contain packages of 1 and 5; Zimmer U.K. Ltd., Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio.
Manufacturer
Zimmer Inc.

Device Recall Zimmer H.A.S. Autotransfusion System H.A.S. Kit with 1/8" Drain

Model / Serial
All lots manufactured on or before 1/18/08. Product has a 5 year expiration period.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia, Canada, Chile, China, Czech Republic, Dubai, Ecuador, France, Germany, Greece, Hungary, Italy, Japan, Korea, Poland, Romania, Russia, Saudi Arabia, Serbia & Montenegro, Singapore, Slovakia, South Africa, Spain, and Switzerland.
Product Description
Zimmer H.A.S. Autotransfusion System, H.A.S. Kit with 1/8" Drain , 3,2mm, 10Fr, PVC, 107cm, medium, sterile, latex free, Rx only; Zimmer, Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio; REF 00-2555-020-05.
Manufacturer
Zimmer Inc.

Device Recall Zimmer H.A.S. Autotransfusion System H.A.S. Kit with 3/16" Drain

Model / Serial
All lots manufactured on or before 1/18/08. Product has a 5 year expiration period.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Australia, Canada, Chile, China, Czech Republic, Dubai, Ecuador, France, Germany, Greece, Hungary, Italy, Japan, Korea, Poland, Romania, Russia, Saudi Arabia, Serbia & Montenegro, Singapore, Slovakia, South Africa, Spain, and Switzerland.
Product Description
Zimmer H.A.S. Autotransfusion System, H.A.S. Kit with 3/16" || Soft Drain , 4,8mm, 15Fr, PVC, 107cm, firm, sterile, latex free, Rx only; Zimmer, Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio; REF 00-2555-030-05.
Manufacturer
Zimmer Inc.

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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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