Drugs & medicalClass I

Jubilant Cadista Pharmaceuticals, Inc. recalls Meclizine Hydrochloride Tablets USP, 12.5 mg, packaged in a case of 24 bottles (100-count bottle), Rx only, Manufactured…

Labeling: Label mix-up: Incorrect label placed on product. Shipper cases labeled Meclizine Hydrochloride Tablets contain bottles incorrectly labeled as PredniSONE Tablets. The tablets in the bottles are Meclizine…

Read the official notice →
Date
2022-04-06
Country
United States
Brand
Jubilant Cadista Pharmaceuticals
Product
Meclizine Hydrochloride Tablets USP, 12.5 mg, packaged in a case of 24 bottles (100-count bottle), Rx only, Manufactured by: Jubilant…
Classification
Class I
Units
Product was distributed in Arkansas, Florida, North Carolina, South Carolina…
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Jubilant Cadista Pharmaceuticals recalls

  1. 2023-01-11
  2. US
    Drugs & medicalClass III

    Jubilant Cadista Pharmaceuticals, Inc. recalls Prochlorperazine Maleate Tablets, USP 5mg, 100 tablets, RX Only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury,…

    Subpotent Drug: Out of specification for assay at the 18-month stability timepoint.

    FDA · DrugJubilant Cadista Pharmaceuticals, Inc.Nationwide in the USA.Official notice →
  3. 2022-08-03
  4. US
    Drugs & medicalClass II

    Jubilant Cadista Pharmaceuticals, Inc. recalls Irbesartan Tablets, USP, 75 mg, 90- count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. Roorkee- 247661,…

    Failed Dissolution Specifications

    FDA · DrugJubilant Cadista Pharmaceuticals, Inc.Nationwide within the United StatesOfficial notice →
  5. US
    Drugs & medicalClass II

    Jubilant Cadista Pharmaceuticals, Inc. recalls Irbesartan Tablets, USP, 150mg, 90- count bottles, Rx only, Manufactured by: Jubilant Generics Ltd. Roorkee- 247661,…

    Failed dissolution specifications.

    FDA · DrugJubilant Cadista Pharmaceuticals, Inc.Nationwide within the United StatesOfficial notice →
  6. 2022-04-13
  7. US
All 5 Jubilant Cadista Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2022-04-06
  2. US
    Drugs & medicalClass II

    Roche Molecular Systems, Inc. recalls cobas LiatSystem, respiratory virus panel nucleic acid assay system, Material Number 07341920190

    Roche has identified a small number of cobas Liat analyzer units that have consistently high noise levels (background signal) originating from the amber detector (used for Influenza B detection). This noise increases…

    FDA · DeviceRoche Molecular Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of CO, IL,…Official notice →
  3. US
    Drugs & medicalClass II

    Mevion Medical Systems, Inc. recalls Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N 10263 or P/N 37808)

    Malfunction of the hand pendant controlling movement of the therapy couch and nozzle may result in unintentional motion. Patient injury is possible if they come in contact with the nozzle or other objects in the…

    FDA · DeviceMevion Medical Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of FL, MO,…Official notice →
  4. US
    Drugs & medicalClass II

    Diagnos Inc recalls CARA (Computer Assisted Retinal Analysis), Product ID: +B543CARA0/$$+7V4.7.2/16D202111179

    Retinal analysis system software has some features, based on artificial intelligence, that potentially lack appropriate market approval, so it is recommended to use a specific prior software version.

    FDA · DeviceDiagnos IncUS: CAOfficial notice →
  5. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Capsules, USP, 30 mg, 90-count bottle, Rx Only, Manufactured By: Dr. Reddy's Laboratories Limited,…

    Failed Dissolution Specifications; during long term stability testing.

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass II

    Aurolife Pharma, LLC recalls Glycopyrrolate Tablets, USP, 1 mg, 100-count bottle, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road,…

    Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.

    FDA · DrugAurolife Pharma, LLCNationwide in the USA and Puerto RicoOfficial notice →
  7. US
    Drugs & medicalClass II

    Drug Depot, Inc., dba APS Pharmacy recalls TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML; Packaged in a multi dose 10ML vial, as a) (CA) 4 ML…

    Lack of sterility assurance.

    FDA · DrugDrug Depot, Inc., dba APS PharmacyNationwide in the USA including Puerto Rico.Official notice →
See all drugs & medical recalls →