Class I · Most seriousActive recall
Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberLot#: T08740, T08742, Exp 06/30/2026
Where it was soldUSA nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Microbial Contamination of Non-Sterile Products
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | GSK Consumer Healthcare, Warren, NJ 07059 |
Show the full FDA record
| Full product label | 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 |
| Distribution | USA nationwide |
| Quantity | 21,900 bottles |
| Recall initiated | 2023-12-26 |
| Report date | 2024-01-31 |
| Recall completed | — |
| Recall number | D-0317-2024 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Warren NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.