Medtronic Disposable Gloves Recalled for Potential Sterility Compromise
Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (sterile surgical gloves) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
The U.S. Food and Drug Administration has issued a recall for Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140. These gloves are components of the custom AMS kit, specifically the Dr. Harrimans Kit (Kit number PSS3600), which is used for general surgery in hospital operating rooms.
The recall was initiated because the gloves may contain splits or holes that could compromise sterility. The affected products were distributed nationwide to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming. The recall involves 120 kits with specific lot numbers and expiration dates: 77213 (6/5/2017), 78414 (7/13/2017), and 79983 (10/20/2017).
Healthcare facilities and consumers should stop using these specific gloves and contact the recalling firm, Windstone Medical Packaging, Inc., for further instructions or replacement.
The recalled product
- Product
- Dr. Harrimans Kit, Kit number PSS3600 convenience custom kits used for general surgery in hospital operating room
- Manufacturer
- Windstone Medical Packaging, Inc.
- Category
- Medical Device — Surgical Gloves
- Hazard
- Affected units
- 120
Distribution
Part of a larger recall action
This product is one of 150 recalled by Windstone Medical Packaging, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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