Cephalexin for Oral Suspension, USP, 250mg/5mL, Rx only, 200mL (when mixed), Each contains cephal...

FDA Recall #D-0540-2024 — Class III — May 10, 2024

Recall #D-0540-2024 Date: May 10, 2024 Classification: Class III Status: Ongoing

Product Description

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.

Reason for Recall

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'

Recalling Firm

Bryant Ranch Prepack, Inc. — Burbank, CA

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

61 Bottles

Distribution

Nationwide in the USA

Code Information

Lot: 235067, Exp 12/31/2025; 235289, Exp 11/30/2025; 235290, Exp 12/31/2025

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated