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Instrapac

ROBINSON HEALTHCARE LIMITED · Model 7083 · UDI-DI 05010058070837

FZT Prescription

510(k) clearances

607

Adverse events

Recalls

255

Facilities

Description

Instrapac Cantilever Nail Cutter 15.5cm/6in x 20

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.