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

Recall Z-0871-2015 — Self-Righting Luer Lock Tip Cap, Green and Self-Righting Luer Slip Tip Cap, Yellow, Baxter Healthcare Corporation, 14445 Grasslands Dr. Englewood, CO 80112 USA. DISCPAC Syringe Tip Caps. RER H93866100 x 1000. Sterile

U.S. FDA — Device Enforcement · United States · 2014-12-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0871-2015
Date of alert
2014-12-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Corporation Englewood
Product category
device
Product type
Devices
Reported risk: Baxter Corporation initiated a recall of two lots of Self-Righting Luer Lock Tip Caps because they were distributed prior to closure of the validation.
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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