Severity
Low
FDA Drug recall · Reported January 1, 2020
Subpotent Drug
Pharmedium Services, LLC recalled NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) … - a low-severity action.
NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) … was recalled by Pharmedium Services, LLC in January 1, 2020. Reason: Subpotent Drug. Check the official notice for the remedy. Verify recall #D-0626-2020 with the FDA Drug before acting.
The recall
Pharmedium Services, LLC issued this low-severity FDA Drug recall-Subpotent Drug.
Sourced from official FDA Drug enforcement records. Verify recall #D-0626-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0626-2020) was formally reported on January 1, 2020, with the manufacturer initiating the action on December 16, 2019. It is classified under Low severity (Class III), with a current status of Terminated. Pharmedium Services, LLC is listed as the recalling firm, operating out of Lake Forest, IL. Federal records list the affected scope as 864 bags.
The documented reason for this recall is: Subpotent Drug Distribution data in the federal record shows the product reached: Nationwide in the U.S.. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
864 bags
Related Recalls
6
5 from same agency
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.
Subpotent Drug
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0626-2020 |
| Date reported | January 1, 2020 |
| Date initiated | December 16, 2019 |
| Recalling firm | Pharmedium Services, LLC |
| Firm location | Lake Forest, IL |
| Affected scope | 864 bags |
| Distribution | Nationwide in the U.S. |
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.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Safecor Health, LLC · 2026-05-27
IntegraDose Compounding Services LLC · 2026-05-27
Lupin Pharmaceuticals Inc. · 2026-05-27
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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 January 1, 2020. 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.