Official recall record
FORWARD Gunshot Wound Kit; Model: AFT-GSW;
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-09-25
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00850056748063
- Brand on record
- INTEGRATED MEDCRAFT LLC
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-11-12.
Record last checked against the registry on 2026-11-12.
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