The Recall Desk
Agency classClass IIOur severity:SevereFDA (Drugs)·D-0018-2027·Announced 2026-10-14

Carolina Infusion Recalls Semaglutide Injectable Due to Sterility Concerns

Carolina Infusion, LLC is recalling Semaglutide 3 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II due to a lack of assurance of sterility in the compounded injectable product. The source does not report any illnesses, injuries, or deaths.

Plain-English summary

Carolina Infusion, LLC is recalling Semaglutide 3 mg/mL injectable, 8 x 0.1 mL syringes. The recall is due to a lack of assurance of sterility, which is related to the formulation using bacteriostatic water and the processing equipment used in the compounded product.

The affected product is identified by Lot 08262026@6 with a beyond-use date of 10/10/2026. The product was distributed nationwide within the U.S.

Consumers should stop using the recalled product and contact their healthcare provider or pharmacist for guidance on next steps.

The recalled product

Product
SEMAGLUTIDE 3 MG/ML INJECTABLE, 8 x 0.1 mL syringes, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot: 08262026@6
  • BUD:10/10/2026.

Distribution

Distributed nationwide across the United States.

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