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

Recall Z-1936-2021 — ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174

U.S. FDA — Device Enforcement · United States · 2021-03-16 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1936-2021
Date of alert
2021-03-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Cardinal Health Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
353885009713
Reported risk: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.