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ACE SURGICAL SUPPLY CO., INC. · Model 0030012 · UDI-DI 00614950008797
FPX
Prescription
10
510(k) clearances
64
Adverse events
1
Recalls
33
Facilities
Description
ACE EXTENSION TUBE 12" STER 2CC VOLUME L/F 100/CA
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-07-18 | Aspen Surgical Products, Inc. | Aspen Surgical is recalling Wound Closures because firm could not confirm sterility, after FDA sampling indicated the product may not be sterile. Using the recalled product could l |
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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.