The Recall Desk
HighFDA (Devices)·Z-1290-2017·Announced 2017-03-08

Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES in Aligned Medical Solutions kits 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 is classified as FDA Class II, and the hazard involves compromised sterility in medical devices, which poses a risk of harm even though no specific injuries or illnesses are reported in the source text.

Plain-English summary

Windstone Medical Packaging, Inc. is recalling Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES that are part of custom Aligned Medical Solutions (AMS) kits. The recall is due to the possibility that the gloves may contain splits or holes, which could compromise their sterility.

The affected product is the Dr Bragg Vein Tray - RX, part number 007912-8. A total of 120 kits were distributed to locations in Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Nebraska, New Jersey, Nevada, Ohio, Pennsylvania, Texas, Utah, Virginia, and Washington.

Specific lot numbers and expiration dates for the recalled items include 86735 (9/14/2017), 87662 (7/12/2018), 88455 (12/18/2017), 95528 (1/3/2018), 96110 (6/6/2018), and 99457 (7/1/2018). Users should check their inventory for these specific lot numbers and stop using the affected gloves if found.

The recalled product

Product
Dr Bragg Vein Tray - RX, part number 007912-8
Manufacturer
Windstone Medical Packaging, Inc.
Category
Medical Device — Surgical/Procedural Supplies
Hazard
Affected units
120

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 (7)

  • Lot number and expiration date 86735
  • 9/14/2017 87662
  • 7/12/2018 88455
  • 12/18/2017 95528
  • 1/3/2018 96110
  • 6/6/2018 99457
  • 7/1/2018

Distribution

Distributed in 26 states:

Part of a larger recall action

This product is one of 124 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 124 products in this recall →

Related recalls

Same manufacturer · Windstone Medical Packaging, Inc.

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Same hazard · sterility compromise

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