The Recall Desk
ModerateFDA (Drugs)·D-0995-2015·Announced 2015-05-20

Akorn Recalls Sulfamethoxazole and Trimethoprim Oral Suspension for Dissolution Failure

Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole failed to meet dissolution specifications.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically involves a situation where use of, or exposure to, a violative product may cause temporary or medically reversible health consequences. The specific defect is a failure to meet dissolution specifications, which is a quality control issue rather than a contamination or mislabeling hazard involving immediate physical harm.

Plain-English summary

Akorn, Inc. is recalling 27,648 bottles of Sulfamethoxazole and Trimethoprim Oral Suspension, USP, 200 mg/40 mg per 5mL, Cherry Flavor, 16 fl oz (473 mL) bottles. The product is identified by NDC 50383-0823-16 and was manufactured by Hi-Tech Pharmacal Co. Inc. The affected lots are #623940 (Exp. 10/2015), #624487 (Exp. 11/2015), #624741 (Exp. 11/2015), and #625296 (Exp. 1/2016).

The recall was initiated because the product failed to meet dissolution specifications for sulfamethoxazole. This means the active ingredient may not dissolve at the required rate, potentially affecting the medication's effectiveness.

The affected product was distributed nationwide and in Puerto Rico. Consumers and healthcare providers should check their inventory for the specific lot numbers and expiration dates listed above. If the product is found, it should be returned to the pharmacy or supplier for a refund or replacement.

The recalled product

Product
SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION, USP,200 mg/ 40 mg per 5mL, CHERRY FLAVOR, 16 fl oz (473 mL) bottles (NDC 50383-0823-16), Rx only, HI-TECH PHARMACAL CO. INC, Amityville, NY 11701
Manufacturer
Akorn, Inc.
Category
Drug — Antibiotic
Hazard

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 (7)

  • Lot # 623940
  • Exp. 10/2015
  • Lot # 624487
  • Exp. 11/2015
  • Lot # 624741
  • Lot # 625296
  • Exp. 1/2016

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 3 recalled by Akorn, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

Related recalls

Same manufacturer · Akorn, Inc.

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Same hazard · dissolution failure

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