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

Recall Z-2388-2015 — Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.

U.S. FDA — Device Enforcement · United States · 2015-07-07 · 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-2388-2015
Date of alert: 2015-07-07
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: C.R. Bard, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 53620387

Reported risk: Potential breach of the sterile barrier packaging.

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.

Recall Z-2388-2015 — Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.

Related