The Recall Desk
HighFDA (Devices)·Z-0200-2017·Announced 2016-10-26

Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because they may contain splits or holes that 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 is classified as FDA Class II. The hazard involves a risk of harm (compromised sterility) in a medical device where injury has not yet been reported, fitting the criteria for a High severity score.

Plain-English summary

Medtronic is recalling COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, which are part of the custom AMS kit. The recall was initiated because the gloves may contain splits or holes that compromise sterility.

The affected gloves are part of the GYN Lap Pack, Kit number PSS2194(B, which are convenience custom kits used for general surgery in hospital operating rooms. The recall involves 20 kits with lot numbers 73774 (expiration date 2/6/2016) and 73292 (expiration date 2/21/2016).

The products were distributed nationwide to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming. Windstone Medical Packaging, Inc. is the recalling firm. Healthcare facilities should stop using the affected gloves and contact the manufacturer for instructions on return or disposal.

The recalled product

Product
GYN Lap Pack, Kit number PSS2194(B convenience custom kits used for general surgery in hospital operating room
Manufacturer
Windstone Medical Packaging, Inc.
Category
Medical Device — Surgical Gloves
Hazard
Affected units
20

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot Numbers/ Expiration Dates: 73774 2/6/2016 73292 2/21/2016

Distribution

Distributed nationwide across the United States.

The notice also names 12 states specifically:

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.

See all 150 products in this recall →

Related recalls

Same manufacturer · Windstone Medical Packaging, Inc.

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Same hazard · sterility compromise

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