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

Recall Z-1483-2020 — Teleflex Pilling Aortic Punch, 4.0mm. Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit - Product Usage: This device is used for cardiovascular surgical procedures.

U.S. FDA — Device Enforcement · United States · 2020-02-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1483-2020
Date of alert
2020-02-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Deroyal Industries, Inc. Lafollette
Product category
device
Product type
Devices
Reported risk: The sterile packaging has the potential to be compromised.
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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