NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection… — Class III drug recall D-0626-2020
Terminated recall by Pharmedium Services, LLC, reported 2020-01-01, distributed nationwide. Subpotent Drug
| Recall number | D-0626-2020 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2019-12-16 |
| Classified | 2019-12-23 |
| Reported by FDA | 2020-01-01 |
| Terminated | 2021-02-09 |
| Distributed | Nationwide (US) |
| Quantity | 864 bags |
| Reason classes | potency |
| Lot numbers | 193040035S, 193120031S, 193150024S, 193180030S, 193240028S, 193250022S |
| Expiration dates | 2019-12-29, 2020-01-08, 2020-01-09, 2020-01-12, 2020-01-18, 2020-01-19 |
Product
NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
Reason for recall
Subpotent Drug
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-0626-2020. 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.