Norepinephrine 4 mg — Class I drug recall D-0003-2019
Terminated recall by QuVa Pharma, Inc., reported 2018-09-26, distributed nationwide. Subpotent Drug: Product may not have the active ingredient present in the bag.
| Recall number | D-0003-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | QuVa Pharma, Inc., Sugar Land, TX, United States |
| Recall initiated | 2018-08-27 |
| Classified | 2018-10-01 |
| Reported by FDA | 2018-09-26 |
| Terminated | 2019-04-02 |
| Distributed | Nationwide (US) |
| Quantity | 528 bags |
| Reason classes | potency |
| Lot numbers | 30000271 |
| Expiration dates | 2018-10-01 |
Product
Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx only, QuVa Pharma, 519 Route 173, Bloombury, NJ 08804, UPC 70092103417.
Reason for recall
Subpotent Drug: Product may not have the active ingredient present in the bag.
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-0003-2019. 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.