Robitussin Honey CF Max Nighttime Adult recall: Sterility Concern
Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059
Why was Robitussin Honey CF Max Nighttime Adult recalled?
Microbial Contamination of Non-Sterile Products
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot#: T08740, T08742, Exp 06/30/2026
- Product
- Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059
- Recalling firm
- Haleon US Holdings LLC
- Quantity
- 21,900 bottles
- Distribution
- USA nationwide
- Recall date
- January 31, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)