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

Recall Z-1682-2019 — RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

U.S. FDA — Device Enforcement · United States · 2019-04-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1682-2019
Date of alert
2019-04-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
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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