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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

Angio Pack, part number AMS6711

Windstone Medical Packaging

Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →

Morris Lap Pack, part number PSS3199(A

Windstone Medical Packaging

Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →

Universal Pack, part number AMS2036

Windstone Medical Packaging

Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Infusion Pumps Nationwide View Details →
Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →
Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →
Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →

Hernia Pack, part number AMS3859

Windstone Medical Packaging

Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →

Stem Pack, part number AMS5166

Windstone Medical Packaging

Class I - Dangerous

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Jan 11, 2017 Other Medical Devices Nationwide View Details →

Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.

Jan 5, 2016 Implants & Prosthetics View Details →

Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.

Jan 5, 2016 Implants & Prosthetics View Details →

Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.

Jan 5, 2016 Implants & Prosthetics View Details →

The monitor may not alarm appropriately for a pediatric or neonatal patient.

Jan 17, 2017 Diagnostic Equipment View Details →

Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.

Jan 5, 2016 Implants & Prosthetics View Details →