PlainRecalls
FDA Devices Moderate Class II Terminated

BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)

Reported: November 27, 2019 Initiated: October 14, 2019 #Z-0500-2020

Product Description

BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)

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

Units Affected
967,680
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: 306575 (Canada only). Recalled by Becton Dickinson & Company. Units affected: 967,680.
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-0500-2020.