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V. Mueller

STERIS CORPORATION · Model SU15120 · UDI-DI 10885403066009

FZT Prescription

510(k) clearances

609

Adverse events

Recalls

254

Facilities

Description

NAIL NIPPER CONCAVE EDGE, DOUBLE SPRING OVERALL LENGTH 5-3/4 inches 14.5CM

Recalls

Date	Firm	Reason
2024-12-03	Sklar Instruments	Reports of various packaging issues that may result in a breach of the sterile barrier.
2010-06-04	Maquet Cardiovascular	Pouch integrity may be compromised, resulting in loss of sterility.
2008-04-24	Ethicon Endo-Surgery Inc	The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.
2008-04-24	Ethicon Endo-Surgery Inc	The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.
2008-04-24	Ethicon Endo-Surgery Inc	The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.
2008-04-24	Ethicon Endo-Surgery Inc	The firm discovered a component production issue which may cause the cartridge to deploy an incomplete staple line.

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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.