NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection… — Class III drug recall D-0625-2020
Terminated recall by Pharmedium Services, LLC, reported 2020-01-01, distributed nationwide. Subpotent Drug
| Recall number | D-0625-2020 |
|---|---|
| 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 | 5,820 bags |
| Reason classes | potency |
| Lot numbers | 192930039S, 192930041S, 192940048S, 192940049S, 192950031S, 192950032S, 192960039S, 192960040S, 192960041S, 192960042S, 192970034S, 192970036S, 192970037S, 192980043S, 192980044S, 192980045S, 193010042S, 193020042S, 193030039S, 193030040S, 193030049S, 193040045S, 193040046S, 193040047S, 193080040S, 193080041S, 193080042S, 193080043S, 193080044S, 193090034S, 193090035S, 193090036S, 193100041S, 193100042S, 193100043S, 193120036S, 193150028S, 193170033S, 193170034S, 193170035S and 10 more |
| Expiration dates | 2019-12-18, 2019-12-19, 2019-12-20, 2019-12-22, 2019-12-25, 2019-12-26, 2019-12-27, 2019-12-28, 2019-12-29, 2020-01-02, 2020-01-03, 2020-01-04, 2020-01-08, 2020-01-09, 2020-01-11, 2020-01-12, 2020-01-15, 2020-01-16, 2020-01-17, 2020-01-18, 2020-01-19, 2020-01-30 |
Product
NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 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-0625-2020. 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.