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Shur-Strip®
Derma Sciences Canada Inc · Model 81121 · UDI-DI 00809958181515
10
510(k) clearances
64
Adverse events
1
Recalls
29
Facilities
Description
Shur Strip Sterile Skin Closures
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.