Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Ranitidine Syrup (Ranitidine Oral Solution Recalled by Bio-pharm, Inc. Due to Failed Impurities/Degradation Specifications: Product recalled due to elevated...

Date: December 17, 2015
Company: Bio-pharm, Inc.
Status: Terminated
Source: FDA (Drug)

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 Bio-pharm, Inc. directly.

Affected Products

Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5 mL), 16 fl oz Bottle, Rx only, Mfd For: Heritage Pharmaceuticals Inc., Eatontown, NJ 07724, NDC 23155-291-51

Quantity: 103,664 Bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications: Product recalled due to elevated impurity result detected during routine stability testing.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Bio-pharm, Inc.

Bio-pharm, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report