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Becton Dickinson & Company recalls BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Recalled November 27, 2019 · FDA recall Z-0499-2020 · Becton Dickinson &
Hazard
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes. · FDA Class II
Units
1,632,000
Sold at
Distribution US Nationwide and Canada
Description
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Product
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →