FDA recall Z-0500-2020

Product

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.

Distribution

Distribution US Nationwide and Canada

Key facts

Status

Terminated

Initiation date

2019-10-14

Report date

2019-11-27

Termination date

2020-10-16

Voluntary/Mandated

Voluntary: Firm initiated

Location

Franklin Lakes, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0500-2020