Recall RadarIMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord BioPharma Inc., 8041 Arco corporate Drive, Suite 200, Raleigh, NC…
Lack of assurance of Sterility:
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- ACCORD BIOPHARMA INC — Raleigh, NC
- Severity
- Class II — moderate
- Reported
- July 8, 2026
- Quantity
- 326 vials
- Recall number
- D-0653-2026
- Status
- Ongoing
- Source
- FDA
Where it went
US Nationwide.
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