All Recalls

95,083 total recalls in our database

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 →

Augmentation Pack, part number AMS6370

Windstone Medical Packaging

🏥 Medical Devices 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 →

These items are incorrectly etched and labeled. The item etched and labeled as 10mm Strut 03.820.350 lot 5919005 is a 12 mm Strut. The item etched and labeled as 12 mm Strut 03.820.352 lot 5919006 is a 10 mm Strut.

Jan 31, 2017 Surgical Instruments View Details →
🏥 Medical Devices 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 →
🏥 Medical Devices 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 Implants & Prosthetics Nationwide View Details →

GYN Pack, part number AMS4013(A

Windstone Medical Packaging

🏥 Medical Devices 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 probe misalignment or bending has the potential to lead to delay in reporting results or incorrect patient results.

Jan 30, 2017 Diagnostic Equipment Nationwide View Details →

Lap Pack, part number AMS4801

Windstone Medical Packaging

🏥 Medical Devices 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 →
🏥 Medical Devices 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 →

Opgrande Hand Pack, part number AMS4767

Windstone Medical Packaging

🏥 Medical Devices 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 →
🏥 Medical Devices 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 →

Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.

Feb 1, 2017 Diagnostic Equipment Nationwide View Details →

Chest Breast Drape, part number AMS5853

Windstone Medical Packaging

🏥 Medical Devices 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 →

Olympus has received complaints regarding the breakage of the endoscope's insertion tube bending section during surgical procedures. Some of these complaints are associated with tissue trauma, including perforation, and insertion tubes which were stuck inside the patient and had to be surgically removed.

Dec 12, 2016 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

Olympus is recalling the URF-P6/P6R endoscopes due to a similar device (URF-V2/V2R endoscopes) but not identical, where adverse event complaints associated with tissue trauma, perforation and insertion tubes which were stuck inside of patients that had to be surgically removed. In an effort to mitigate a potential risk to patient health, Olympus is undertaking this action to notify users of these complaints and the need for careful inspection of the endoscope prior to use in accordance with the instructions provided int heir notification letter.

Dec 12, 2016 Other Medical Devices Nationwide View Details →