Bryant Ranch Prepack, Inc. recalls Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed), Each contains: cephalexin monohydrate,
Bryant Ranch Prepack recalls 125mg/5mL cephalexin suspension due to incorrect labeling. The label states 2.5g instead of 5g per bottle. This may lead to incorrect dosing.
Lower-risk recall
Labeling: Not Elsewhere Classified: Back label states Each contains: cephalexin monohydrate, USP equivalent to 2.5g' instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 5g
Contact the company & request your remedy
What happened, in plain English
Bryant Ranch Prepack is recalling cephalexin oral suspension because the label incorrectly states it contains 2.5g of cephalexin instead of 5g per bottle. This labeling error could lead to incorrect dosing if the product is used without checking the label. Read more at govinfonow.com/recall/32682-bryant-ranch-prepack-cephalexin-suspension-recall-labeling-error.
Source Summary by GovInfoNow · govinfonow.com/recall/32682-bryant-ranch-prepack-cephalexin-suspension-recall-labeling-error · Updated September 23, 2026 · FDA enforcement record: FDA #D-0537-2024
Cite this page
“Bryant Ranch Prepack Cephalexin Suspension Recall: Labeling Error.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32682-bryant-ranch-prepack-cephalexin-suspension-recall-labeling-error. Based on FDA recall #D-0537-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0537-2024%22&limit=1).
Why it’s dangerous
The label states each bottle contains 2.5g of cephalexin instead of the intended 5g. This labeling error could result in underdosing if the product is used without checking the label, potentially leading to ineffective treatment.
Who’s affected
Prescription holders of this antibiotic suspension who received it from a pharmacy or doctor. Patients using the product without verifying the label may be at risk of incorrect dosing.
How to tell if you have this one
Check for the product name 'Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed)' on the label. Look for the manufacturer 'Bryant Ranch Prepack, Inc' and NDC number 63629-9205-1.
- Brand
Bryant Ranch Prepack- Category
Drug
All 5 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Ongoing- Distribution
Nationwide in the USA
| Recall number | Product, codes & lots | Quantity | NDC |
|---|---|---|---|
| D-0536-2024 | Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 100 Tablets, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9204-1.; Lot:225541, 226866, 227369, 227519, 229845, 231422, 234889, Exp: 03/31/2025 | 156 bottles | 63629-9204-1 |
| D-0537-2024 | Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed), Each contains: cephalexin monohydrate, USP equivalent to 2.5g of cephalexin in a strawberry flavored mixture. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9205-1.; Lot:234892, Exp:02/28/2025. | 6 bottles | 63629-9205-1 |
| D-0538-2024 | Cephalexin for Oral Suspension, USP, 250mg/ 5mL, Rx only, 200mL (when mixed), Each contains cephalexin monohydrate, USP equivalent to 5g cephalexin. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-8858-1.; Lot: 235287, 235629, 235805, 236292, 237022, 237308, 237748, Exp: 12/31/2025; | 104 bottles | 63629-8858-1 |
| D-0539-2024 | Cephalexin for Oral Suspension, USP, 250mg per 5mL, Rx only, 100mL (when mixed), Each contains cephalexin monohydrate, USP equivalent to 5g cephalexin. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9206-1.; Lot: 235288, 235294, 235368, 235806, 236058, 236138, 236139, 236351, 236490, 236757, 236877, Exp:11/30/2025; 236758, 236762, 237254, 237349, 237401, 237807, Exp: 12/31/2025. | 190 bottles | 63629-9206-1 |
| D-0540-2024 | Cephalexin for Oral Suspension, USP, 250mg/5mL, Rx only, 200mL (when mixed), Each contains cephalexin monohydrate, USP equivalent to 5g cephalexin. Manufactured by Alkem Laboratories Ltd, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504, NDC 63629-9207-1.; Lot: 235067, Exp 12/31/2025; 235289, Exp 11/30/2025; 235290, Exp 12/31/2025 | 61 Bottles | 63629-9207-1 |
What to do — step by step
Check Label
Verify the label states 'Each contains: cephalexin monohydrate, USP equivalent to 2.5g' instead of 5g per bottle.
Questions people ask
Why is this product being recalled?
The label incorrectly states each bottle contains 2.5g of cephalexin instead of 5g per bottle, which could lead to incorrect dosing.
How can I tell if I have the recalled product?
Check for the product name 'Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed)' and the manufacturer 'Bryant Ranch Prepack, Inc' with NDC 63629-9205-1.
What should I do if I have the recalled product?
Check the label to confirm the dosage. If the label states 2.5g instead of 5g, contact your doctor or pharmacist for guidance.
Contact Bryant Ranch Prepack
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-0537-2024 — Bryant Ranch Prepack Bryant Ranch Prepack Hello, I own a Bryant Ranch Prepack that is covered by recall D-0537-2024 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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Where this comes from
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.
- Official source: FDA Recall #D-0537-2024 (May 10, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0537-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.