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

Recall Z-0925-2022 — Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30 Priority Pack w/.115 RHV - REF 1000185-115 WPL2122279-01 (2019-03-01)

U.S. FDA — Device Enforcement · United States · 2022-03-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0925-2022
Date of alert
2022-03-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Abbott Vascular
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
8717648013607
Reported risk: Due to an increase in complaint trend for leaks and intermittent/loose connections.
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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