FDA Drug recall D-1162-2014
5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA,…
- FDA Drug
- Class I
- terminated
- Published 2014-03-26
On 2014-03-26 the FDA classified a Class I recall of 5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA,… by Baxter Healthcare, citing presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fiber….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1162-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-11-21 |
| Published | 2014-03-26 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product code 2B0089, NDC 0338-0017-38.
Reason
Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene and human hair embedded in the plastic bag
Identifiers
| ndc | 0338-0017-10 |
|---|---|
| ndc | 0338-0017-41 |
| ndc | 0338-0017-11 |
| ndc | 0338-0017-31 |
| ndc | 0338-0017-48 |
| ndc | 0338-0017-18 |
| ndc | 0338-0017-38 |
| ndc | 0338-0017-02 |
| ndc | 0338-0017-03 |
| ndc | 0338-0017-04 |
| ndc | 0338-0023-02 |
| ndc | 0338-0023-03 |
| ndc | 0338-0023-04 |
| code_info | Lot #: P285288, Exp 11/13 |
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-1162-2014%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.