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

Recall Z-1256-2021 — JUDKINS PACK

U.S. FDA — Device Enforcement · United States · 2021-02-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1256-2021
Date of alert
2021-02-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health 200, LLC
Product category
device
Product type
Devices
Reported risk: Component Part Number: 19537LBL (LBL, SHEET OF 39, ASSORTED, STDSZ, MULTI W/BLK INK, WATERPROOF) is being reported as intermittently mixed with an incorrect medication label sheet throughout the specific Presource¿ kit SANHDJTVCF Judkins Pack lot # 525067.
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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