Severity
Moderate
ModerateClass IICompleted
FDA Drug recall · Reported September 29, 2021
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-621-16
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Morton Grove Pharmaceuticals, Inc. recalled Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured … - a moderate-severity action.
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured … was recalled by Morton Grove Pharmaceuticals, Inc. in September 29, 2021. Reason: CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with mi…. Check the official notice for the remedy. Verify recall #D-0816-2021 with the FDA Drug before acting.
The recall
Morton Grove Pharmaceuticals, Inc. issued this moderate-severity FDA Drug recall-CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with mi….
- Moderate
- severity level
- Class II
- classification
- September 29, 2021
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0816-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0816-2021) was formally reported on September 29, 2021, with the manufacturer initiating the action on September 3, 2021. It is classified under Moderate severity (Class II), with a current status of Completed. Morton Grove Pharmaceuticals, Inc. is listed as the recalling firm, operating out of Morton Grove, IL. Federal records list the affected scope as 38,748 bottles.
The documented reason for this recall is: CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms. Distribution data in the federal record shows the product reached: Nationwide USA and China. 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.
Drugs & Medications recalls over time
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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
38,748 bottles
Related Recalls
6
5 from same agency
Product description
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-621-16
Reason for recall
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | D-0816-2021 |
| Date reported | September 29, 2021 |
| Date initiated | September 3, 2021 |
| Recalling firm | Morton Grove Pharmaceuticals, Inc. |
| Firm location | Morton Grove, IL |
| Affected scope | 38,748 bottles |
| Distribution | Nationwide USA and China |
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.
- Check the recall number (D-0816-2021) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-621-16. Recalled by Morton Grove Pharmaceuticals, Inc.. Units affected: 38,748 bottles.
Why was this product recalled? ▼
CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 29, 2021. Severity: Moderate. Recall number: D-0816-2021.
Where was the recalled product distributed? ▼
Distribution: Nationwide USA and China.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0816-2021) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3…
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FDA Drug Moderate
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
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 29, 2021. 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.