Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2496-2019 — CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in general surgery and gynecologic procedures where ligation and division of vessels is desired.

U.S. FDA — Device Enforcement · United States · 2019-08-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2496-2019
Date of alert
2019-08-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Aesculap Implant Systems LLC
Product category
device
Product type
Devices
Reported risk: possibility of the sterility batch being insufficiently sterilized
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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