Haleon recalls Robitussin Honey CF Max Nighttime Adult due to microbial contamination
Haleon recalls Robitussin Honey CF Max Nighttime Adult bottles with microbial contamination risk. Affected lots expire June 2026. Consumers should stop using and contact Haleon for details.
Stop using this now
Microbial Contamination of Non-Sterile Products
Contact the company
What happened, in plain English
Haleon is recalling Robitussin Honey CF Max Nighttime Adult bottles that may contain microbial contamination. This poses a risk of infection or illness if consumed. Affected bottles have specific lot numbers and expiration dates. Read more at govinfonow.com/recall/32909-haleon-recalls-robitussin-honey-cf-max-nighttime-adult-due-to.
Source Summary by GovInfoNow · govinfonow.com/recall/32909-haleon-recalls-robitussin-honey-cf-max-nighttime-adult-due-to · Updated September 23, 2026 · FDA enforcement record: FDA #D-0317-2024
Cite this page
“Haleon recalls Robitussin Honey CF Max Nighttime Adult due to microbial contamination.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32909-haleon-recalls-robitussin-honey-cf-max-nighttime-adult-due-to. Based on FDA recall #D-0317-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0317-2024%22&limit=1).
Why it’s dangerous
Microbial contamination means harmful bacteria or other microorganisms may be present in the product. If consumed, this could cause infection or illness. The product is non-sterile, so contamination is possible during manufacturing.
Who’s affected
Adults who purchased Robitussin Honey CF Max Nighttime Adult bottles with lot numbers T08740 or T08742, expiring June 30, 2026, are affected. Children and infants should not use this product.
How to tell if you have this one
Check the bottle label for lot numbers T08740 or T08742. The product expires June 30, 2026. This product is distributed by GSK Consumer Healthcare.
- Brand
Haleon- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
USA nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0316-2024 | Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059; a) Lot#: T10810, Exp 10/31/2025 b) Lot#: T08730, T08731, T08732, T08733, Exp 05/31/2025; T10808, Exp 09/30/2025 | a) 31,632 bottles; b) 336,528 bottles |
| D-0317-2024 | 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; Lot#: T08740, T08742, Exp 06/30/2026 | 21,900 bottles |
What to do — step by step
Stop Using Now
Immediately stop using the recalled Robitussin Honey CF Max Nighttime Adult bottles with lot numbers T08740 or T08742.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “USA nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.8 years after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Other Haleon recalls
Latest drug recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0317-2024 (December 26, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0317-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.