Becton Dickinson & Company recalls BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
- Recall date
- October 14, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0499-2020
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- Distribution US Nationwide and Canada
Why it was recalled
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
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