0 — Class I drug recall D-1550-2014
Terminated recall by Baxter Healthcare Corp., reported 2014-08-27, distributed nationwide. Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes
| Recall number | D-1550-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp., Deerfield, IL, United States |
| Recall initiated | 2014-05-12 |
| Classified | 2014-08-21 |
| Reported by FDA | 2014-08-27 |
| Terminated | 2015-06-29 |
| Distributed | Nationwide (US) |
| Quantity | 4,200 containers |
| Reason classes | specification failure |
| Lot numbers | C931923 |
| Expiration dates | 2015-08-31 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1550-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.