Robitussin Honey CF Max Nighttime Adult — Class I drug recall D-0317-2024
Ongoing recall by Haleon US Holdings LLC, reported 2024-01-31, distributed nationwide. Microbial Contamination of Non-Sterile Products
| Recall number | D-0317-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Haleon US Holdings LLC, Warren, NJ, United States |
| Recall initiated | 2023-12-26 |
| Classified | 2024-02-07 |
| Reported by FDA | 2024-01-31 |
| Distributed | Nationwide (US) |
| Quantity | 21,900 bottles |
| Reason classes | microbial contamination, sterility |
| Lot numbers | T08740, T08742 |
| Expiration dates | 2026-06-30 |
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
Reason for recall
Microbial Contamination of Non-Sterile Products
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0317-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.