Reported Oct 21, 2026 · Ongoing · Updated Oct 26, 2026

FORWARD Gunshot Wound Kit; Model: AFT-GSW;

Integrated Medcraft LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: INTEGRATED MEDCRAFT LLC · 1 Sinco Pl Unit A10 · East Hampton, CT · 06424-2129

Is this the product you have?

  • FORWARD Gunshot Wound Kit
  • ModelAFT-GSW
Lot codes and dates

3 of 3 products

Products covered by this recall
#BarcodesProduct as published
1Model: ATF-GSW
200850056748063UDI-DI: 00850056748063
3Lot Numbers: IMC-00000024, IMC-00000034, IMC-00000053, IMC-00000056, IMC-00000076, IMC-00000081, IMC-00000082, IMC-00000083, IMC-00000084, IMC-00000085, IMC-00000094, IMC-00000148, IMC-00000149, IMC-00000152, IMC-00000153, IMC-00000154, IMC-00000173, IMC-00000174, IMC-00000179, IMC-00000186, IMC-00000187
Amount recalled
1033

Where it was sold

Why it was recalled

Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad to degrade over time. The degradation may cause remnants of the nonwoven pad material to dislodge on the wound or in close proximity to the wound.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 12:10 AM UTC

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