FDA Drug recall D-0958-2016
Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only,…
- FDA Drug
- Class I
- terminated
- Published 2016-06-15
On 2016-06-15 the FDA classified a Class I recall of Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only,… by Baxter Healthcare, citing presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0958-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-12-15 |
| Published | 2016-06-15 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0719-06
Reason
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Identifiers
| ndc | 0338-0719-06 |
|---|---|
| code_info | Lot # C985150; Exp. 07/16 |
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-0958-2016%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.