Quick Facts at a Glance
- Recall Date
- May 27, 2026
- Hazard Level
- HIGH
- Brands
- ARIPIPRAZOLE, Ajanta Pharma USA Inc.
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- ARIPIPRAZOLE, Ajanta Pharma USA Inc.
- Model numbers
- Lot: PA00805, expires: 01/31/2029
- UPC codes
- 27241-051, 27241-052, 27241-053, 27241-054, 27241-055, 27241-056, 27241-051-03, 27241-051-08 +8 more
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 27, 2026
Reported by FDA DRUG
June 24, 2026
RecallRadar source check
June 30, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Ajanta Pharma USA Inc or your healthcare provider for guidance. Notification method: Letter
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Full Description
Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-056-03.. Generic: ARIPIPRAZOLE; Brand: ARIPIPRAZOLE. Reason: Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.. Classification: Class II. Quantity: 6,143 bottles. Distribution: U.S. Nationwide
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Safety Guide
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