Cetirizine HCL tablets recalled for manufacturing process deviations
Glenmark Pharmaceuticals is voluntarily recalling Cetirizine HCL 10mg tablets distributed nationwide. The recall was initiated due to Current Good Manufacturing Practice deviations.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is a voluntary precautionary recall due to manufacturing process deviations. Per the severity rubric, voluntary precautionary recalls are classified as Moderate.
Plain-English summary
Glenmark Pharmaceuticals Inc. is recalling Cetirizine HCL 10mg tablets in 365-count packs distributed nationwide through retailers including Amazon and Walmart, with NDC# 72657-129-35.
The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. This is a voluntary recall initiated by the manufacturer.
Affected lot numbers include 17231980, 17232044, 17241436, 17241437, 17241455, 17241456, 17241457, 17241892, and 17241893, with expiration dates ranging from August 2025 to October 2026. Consumers should check their product packaging to determine if their medication is affected.
If you have this product, do not use it and return it to the place of purchase. Consult your healthcare provider if you have questions about your medication.
The recalled product
- Product
- CETIRIZINE HCL (CETIRIZINE)
- Brand
- CETIRIZINE HCL
- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- Category
- Drug
- Hazard
- cgmp-deviation
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (10)
- Lot # 17231980
- ep.. date Aug-25 Amazon 17232044
- ep.. date Aug-25 Walmart 17241436
- ep.. date Jul-26 Amazon 17241437
- ep.. date Jul-26 Amazon 17241455
- ep.. date Jul-26 Amazon 17241456
- ep.. date Aug-26 Amazon 17241457
- ep.. date Aug-26 Amazon 17241892
- ep.. date Oct-26 Amazon 17241893
- ep.. date Oct-26 Amazon
UPCs (2)
- 0372657128353
- 0372657129350
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- ModerateFDA Recalls Pred Mild Ophthalmic Suspension Due to Failed Stability Specifications
FDA (Drugs) · 2026-06-03
- ModerateNicotine Transdermal System Patches Recalled for Oxidative Impurity Specification Failure
FDA (Drugs) · 2026-06-03
- HighLiraglutide Injection Recalled Due to Particulate Matter in Cartridges
FDA (Drugs) · 2026-05-27
- LowPrimidone Tablets Recalled for Cross-Contamination with Acemetacin
FDA (Drugs) · 2026-05-27