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Home › FDA recalls › TIRZEPATIDE 26 MG/ML INJECTABLE
CLASS II · ModerateFDA

Carolina Infusion, LLC recalls TIRZEPATIDE 26 MG/ML INJECTABLE

📅 Sep 10, 2026 · 📍 Nationwide
Recalling company
Carolina Infusion, LLC
Product
TIRZEPATIDE 26 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;
Reason
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Sep 10, 2026
Reported
Oct 14, 2026
Distribution
Nationwide within the U.S
Status
Ongoing
Quantity
5.6 mLs - in patient specific syringe doses
Lot / codes
Lots: 09012026@3, BUD: 10/16/2026; 08032026@16, BUD: 9/17/2026; 08052026@8, BUD: 9/19/2026; 08072026@13, BUD: 9/21/2026.
Company location
Ridgeland, SC
Recall type
Voluntary: Firm initiated
Recall number
D-0017-2027
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0017-2027 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.