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

Recall Z-2342-2018 — Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery

U.S. FDA — Device Enforcement · United States · 2018-05-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2342-2018
Date of alert
2018-05-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beaver Visitec
Product category
device
Product type
Devices
Reported risk: Blades are loose in handles and may fall out due to non cured epoxy
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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