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

BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547 — recall Z-0499-2020

U.S. FDA — Device Enforcement · United States · 2019-10-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0499-2020
Date of alert
2019-10-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Company
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50382903065474
Reported risk: Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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.