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Aspen® Skin Closure

ASPEN SURGICAL PRODUCTS, INC. · Model 1047NS · UDI-DI 00840113201372

FPX
1
510(k) clearances
64
Adverse events
1
Recalls
28
Facilities

Description

Intended for skin closure and closure support for sutures and staples

Recalls

DateFirmReason
2013-07-18Aspen 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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Data 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.