Severity
Critical
FDA Drug recall · Reported September 26, 2018
Subpotent Drug: Product may not have the active ingredient present in the bag.
QuVa Pharma, Inc. recalled Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx onl… - a critical-severity action.
Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx onl… was recalled by QuVa Pharma, Inc. in September 26, 2018. Reason: Subpotent Drug: Product may not have the active ingredient present in the bag.. Check the official notice for the remedy. Verify recall #D-0003-2019 with the FDA Drug before acting.
The recall
QuVa Pharma, Inc. issued this critical-severity FDA Drug recall-Subpotent Drug: Product may not have the active ingredient present in the bag..
Sourced from official FDA Drug enforcement records. Verify recall #D-0003-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0003-2019) was formally reported on September 26, 2018, with the manufacturer initiating the action on August 27, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. QuVa Pharma, Inc. is listed as the recalling firm, operating out of Sugar Land, TX. Federal records list the affected scope as 528 bags.
The documented reason for this recall is: Subpotent Drug: Product may not have the active ingredient present in the bag. Distribution data in the federal record shows the product reached: Nationwide to hospitals in USA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
528 bags
Related Recalls
6
5 from same agency
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.
Subpotent Drug: Product may not have the active ingredient present in the bag.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0003-2019 |
| Date reported | September 26, 2018 |
| Date initiated | August 27, 2018 |
| Recalling firm | QuVa Pharma, Inc. |
| Firm location | Sugar Land, TX |
| Affected scope | 528 bags |
| Distribution | Nationwide to hospitals in USA |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported September 26, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.