INTEGRATED MEDCRAFT LLC recalls FORWARD Gunshot Wound Kit

Recalling company

INTEGRATED MEDCRAFT LLC

Product

FORWARD Gunshot Wound Kit; Model: AFT-GSW;

Reason

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Sep 25, 2026

Reported

Oct 21, 2026

Distribution

US Nationwide distribution in the states of GA, VA.

Status

Ongoing

Quantity

1033

Lot / codes

Model: ATF-GSW; UDI-DI: 00850056748063; Lot 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;

Company location

East Hampton, CT

Recall type

Voluntary: Firm initiated

Recall number

Z-0147-2027

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0147-2027 in the FDA Enforcement Report. Also see FDA recall press releases.