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TRAUMA BANDAGE
IVF HARTMANN AG · Model 831273 TRAUMA BANDAGE 10 cm · UDI-DI 07611600953608
2
510(k) clearances
70
Adverse events (5 deaths)
6
Recalls
238
Facilities
Description
TRAUMA BANDAGE 10 cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-09-02 | Safeguard US Operating LLC | Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and irrigation, formation of s |
| 2016-02-24 | Amd Ritmed | Product does not meet sterility requirements based on FDA analysis and tested positive for Bacterium Bacillus. |
| 2006-08-16 | International Medsurg Connection, Inc. | The bandages labeled as sterile had not been sterilized prior to distribution. |
| 2006-08-16 | International Medsurg Connection, Inc. | The bandages labeled as sterile had not been sterilized prior to distribution. |
| 2006-08-16 | International Medsurg Connection, Inc. | The bandages labeled as sterile had not been sterilized prior to distribution. |
| 2006-08-16 | International Medsurg Connection, Inc. | The bandages labeled as sterile had not been sterilized prior to distribution. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.