FDA Drug recall D-1550-2014
0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015
- FDA Drug
- Class I
- terminated
- Published 2014-08-27
On 2014-08-27 the FDA classified a Class I recall of 0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015 by Baxter Healthcare, citing presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1550-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-05-12 |
| Published | 2014-08-27 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015
Reason
Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes
Identifiers
| code_info | Lot C931923, exp 8/31/2015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1550-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.