Bryant Ranch Prepack recalls 250mg/5mL cephalexin oral suspension due to incorrect labeling of active ingredient content. This affects specific lots manufactured by Alkem Laboratories Ltd.
Labeling: Not Elsewhere Classified: Back Label states 'Each contains: cephalexin monohydrate, USP equivalent to 5g' instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 10g'
Bryant Ranch Prepack is recalling a specific cephalexin oral suspension product because its label incorrectly states it contains 5g of cephalexin instead of 10g. This labeling error could lead to incorrect dosing if the product is used without proper verification.
The product label incorrectly states each bottle contains 5g of cephalexin monohydrate instead of 10g. This labeling error could result in patients receiving a lower dose than intended if they follow the label without verification.
Prescription holders of the recalled cephalexin suspension (250mg/5mL, 200mL) with specific lot numbers. Patients using this medication for infections may be at risk of incorrect dosing.
Check for the product name 'Cephalexin for Oral Suspension, USP, 250mg/5mL, Rx only, 200mL (when mixed)' with specific lot numbers: 235287, 235629, 235805, 236292, 237022, 237308, 237748. The expiration date is 12/31/2025.
Verify the label states 'Each contains: cephalexin monohydrate, USP equivalent to 5g' instead of 10g.
The product label incorrectly states it contains 5g of cephalexin monohydrate instead of 10g, which could lead to incorrect dosing if used without verification.
The official recall notice does not specify a remedy or action steps beyond checking the label for the labeling error.
Affected lot numbers are 235287, 235629, 235805, 236292, 237022, 237308, 237748.
We’ve drafted a message you can send Bryant Ranch Prepack to request your refund or repair — edit it as you like.
Subject: Recall D-0538-2024 — Bryant Ranch Prepack Bryant Ranch Prepack Hello, I own a Bryant Ranch Prepack that is covered by recall D-0538-2024 from Bryant Ranch Prepack. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
