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Class III: unlikely to cause harmOngoing

Bryant Ranch Prepack Cephalexin for Oral Suspension Recall

Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed), Each c…

Bryant Ranch Prepack, Inc. · Burbank, CA

Risk level
Class III
Reported by FDA
Jun 12, 2024
Recall ID
D-0537-2024
Check your lot numberHow we source this data

Summary

Bryant Ranch Prepack recalled Cephalexin for Oral Suspension starting May 10, 2024. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0537-2024 on Jun 12, 2024. Reason: 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. Status: Ongoing.

Why it was recalled

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

Product description

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 numbers, UPCs & expiration codes

Lot:234892, Exp:02/28/2025.

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0537-2024
Classification
Class III
Status
Ongoing
Recall initiated
May 10, 2024
FDA report date
Jun 12, 2024
Quantity
6 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Bryant Ranch Prepack, Inc.

Original FDA data

Every field from FDA enforcement report D-0537-2024, exactly as published.

Show all FDA fields
City
Burbank
State
CA
Status
Ongoing
Country
United States
Event ID
94605
Address
1919 N Victory Pl
Code information
Lot:234892, Exp:02/28/2025.
Postal code
91504-3425
Report date
Jun 12, 2024
Product type
Drugs
Recall number
D-0537-2024
Classification
Class III
Recalling firm
Bryant Ranch Prepack, Inc.
Product quantity
6 bottles
Reason for 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
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
Nationwide in the USA
Recall initiation date
May 10, 2024
Initial firm notification
Letter
Center classification date
Jun 4, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0537-2024, published Jun 12, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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