FDA recall D-1550-2014

Baxter Healthcare Corp. · Class I · drug

Product

0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015

Reason for recall

Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2014-05-12
Report date: 2014-08-27
Termination date: 2015-06-29
Voluntary/Mandated: Voluntary: Firm initiated
Location: Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1550-2014