Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cephalexin for Oral Suspension Recalled by Preferred Pharmaceuticals, Inc. Due to Failed Impurities/degradation specifications: Repackager recall due to Out...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Preferred Pharmaceuticals, Inc. directly.
Affected Products
Cephalexin for Oral Suspension, Generic for Keflex, USP, Powder for Oral Suspension, 250 mg/5mL, Pkg Size 100, Rx only, Repackaged by Preferred Pharmaceuticals, Inc., Mfg: Ascend Laboratories, LLC, NDC #: 68788-7529-1,
Quantity: Six bottles
Why Was This Recalled?
Failed Impurities/degradation specifications: Repackager recall due to Out of Specification detected by manufacturer for Individual Unidentified Impurity found during related substance test analysis of Cephalexin
Where Was This Sold?
This product was distributed to 1 state: CA
About Preferred Pharmaceuticals, Inc.
Preferred Pharmaceuticals, Inc. has 44 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report