Recall RadarOctreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing: 8-mL vial of 30 mg strength, a pre-filled syringe containing 2…
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
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
- Teva Pharmaceuticals USA, Inc — Parsippany, NJ
- Severity
- Class II — moderate
- Reported
- May 13, 2026
- Quantity
- 2,200 kits
- Recall number
- D-0519-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide in the USA
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