FDA recall record

Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets bottles recall — FDA D-0033-2026

Tablet/Capsules Imprinted with Wrong ID

Class IIIclassification
D-0033-2026official record ID
Oct 29, 2025report date

Recall record at a glance

Official recordD-0033-2026
CategoryDrug Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmJB Chemicals and Pharmaceuticals Ltd
Report dateOct 29, 2025
Recall initiation dateSep 12, 2025
Quantity13,440 bottles
LocationMumbai, India

Official product description

Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-50

Why the product was recalled

Tablet/Capsules Imprinted with Wrong ID

Distribution information

U.S. Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.