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

Recall Z-1705-2017 — The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.

U.S. FDA — Device Enforcement · United States · 2017-03-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1705-2017
Date of alert
2017-03-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Arrow International Inc
Product category
device
Product type
Devices
Reported risk: Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC Kits, that the kits were being recalled due to a labeling error. The lidstock on some of the kits reads CDC-45541-HPK1A, while the banner card on the side of the kit reads CDC-45052-HPK1A. Other kits may list CDC-45052-HPK1A on the lidstock and CDC-45541-HPK1A on the banner card. The affected lot numbers are 23F16C0851, 23F16A0727, and 23F16C0844.
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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