BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Reported: November 27, 2019 Initiated: October 14, 2019 #Z-0499-2020
Product Description
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Reason for Recall
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 1,632,000
- Distribution
- Distribution US Nationwide and Canada
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547. Recalled by Becton Dickinson & Company. Units affected: 1,632,000.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 27, 2019. Severity: Moderate. Recall number: Z-0499-2020.
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