Fexofenadine Hydrochloride Tablets, USP 180mg, Antihistamine, Allergy Recall 2024
FEXOFENADINE HYDROCHLORIDEIssued January 18, 2024Updated Reviewed by the Recall Watch editorial team
FEXOFENADINE HYDROCHLORIDE Fexofenadine Hydrochloride Tablets, USP 180mg, Antihistamine, Allergy, 24 hour, a) 30 Tablets per bottle, NDC 51660-998-30; Distributed by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Made in Indi — recalled per FDA on 1/18/2024. Reason: CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment..
- Agency
- FDA
- Issued
- Jan 18, 2024
- Brand
- FEXOFENADINE HYDROCHLORIDE
- Distribution
- 1 states
- Lots affected
- 5
Steps to take for this recall
Stop using it
Take it out of rotation. Don't consume, wear, or operate.
Verify the match
Compare lot numbers, UPCs, and dates against your product.
Return or dispose
Follow the manufacturer's instructions to refund or safely dispose.
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What's recalled
Fexofenadine Hydrochloride Tablets, USP 180mg, Antihistamine, Allergy, 24 hour, a) 30 Tablets per bottle, NDC 51660-998-30; Distributed by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Made in India, b) 45 Tablets per bottle, NDC 51316-800-45; Distributed by: CVS Pharmacy, Inc., Woonsocket, RI 02895, Made in India, c) 150 Tablets per bottle, NDC 51660-998-55, Distributed by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Made in India.

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Why it was recalled
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Affected products & lot numbers5 lots called out
Affected Lot Numbers
Check your product label — do not use if your lot number appears below.
| Lot Number |
|---|
| Lot #s: a) DNE0792A Exp. 06/31/2025 |
| DNE1027A Exp. 08/31/2025. b) DNE0793A Exp. 06/31/2025. c) DNE0789A |
| DNE0790A |
| DNE0791A Exp. 06/2025 |
| DNE1026A Exp. 08/31/025. |
Where was it sold1 state
Nationwide in the USA
More recalls like this4 related — by brand, contaminant, and category
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Frequently asked questions
Is the FEXOFENADINE HYDROCHLORIDE recall still active?
Yes, this recall is currently active as of January 18, 2024. Do not use or consume the affected product.
What lot numbers are affected?
Affected lot numbers: Lot #s: a) DNE0792A Exp. 06/31/2025, DNE1027A Exp. 08/31/2025. b) DNE0793A Exp. 06/31/2025. c) DNE0789A, DNE0790A, DNE0791A Exp. 06/2025, DNE1026A Exp. 08/31/025.. Check the label on your product.
What should I do if I have the recalled FEXOFENADINE HYDROCHLORIDE?
Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.