Integrated Medcraft FORWARD Gunshot Wound Kit
The Forward Gunshot Wound Kit has a sterile pad that may degrade over time, potentially causing pad remnants to dislodge near a wound.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
INTEGRATED MEDCRAFT LLC began a recall of the FORWARD Gunshot Wound Kit, Model AFT-GSW, on September 25, 2026, due to internal testing identifying an issue affecting the device's sterile pad, potentially causing the pad to degrade over time and remnants to dislodge on or near a wound. The FDA added the recall to its Enforcement Report and classified it on October 9, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI matches.
AFT-GSW
- UDI-DI
- 00850056748063
Details
- Company began the recall
- Event ID
- 99948
- Company
- INTEGRATED MEDCRAFT LLC
- Hazard
- Device defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
