FDAFDA · Food and drugs·Recall number Z-0500-2020
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)
Published November 27, 2019 · Recall initiated: October 14, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Becton Dickinson & Company
- Distributor
- Distribution US Nationwide and Canada
- Lot
- Lot Number: 9175971 UDI: 50382903065757
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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