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

Recall Z-3271-2018 — Bausch + Lomb Stellaris Elite 25 GA Vit Cutter, Model BL5628, 7500 cpm, packaged in sterile pouches, 6/shipper.

U.S. FDA — Device Enforcement · United States · 2018-08-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3271-2018
Date of alert
2018-08-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bausch & Lomb Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00757770058914
Reported risk: The back cap separates from the body of the vitrectomy cutter.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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