Drugs & medicalClass II

Cipla USA, Inc. recalls Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98

Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.

Read the official notice →
Date
2024-11-20
Country
United States
Brand
Cipla
Product
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98
Classification
Class II
Units
USA nationwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Cipla recalls

  1. 2025-12-10
  2. US
    Drugs & medicalClass II

    Cipla Limited recalls Phytonadione Injectable Emulsion, USP 10mg/mL, 10x1 mL Single-Dose Vial/carton, Rx Only, Mfd. by: Cipla Ltd. India At M/s Immacule…

    Failed Stability Specifications: Observed OOS results: eg results for colour index

    FDA · DrugCipla LimitedNationwide in the USAOfficial notice →
  3. 2025-08-27
  4. US
    Drugs & medicalClass III

    Cipla USA, Inc. recalls Albuterol Sulfate, Inhalation Aerosol, 90 mcg, 200 metered Inhalations, NET CONTENT 6.7 g, Manufactured by: Cipla Ltd, Indore, SEZ,…

    Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point.

    FDA · DrugCipla USA, Inc.U.S. Nationwide.Official notice →
  5. 2025-07-30
  6. US
    Drugs & medicalClass II

    Cipla USA, Inc. recalls Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd.…

    Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.

    FDA · DrugCipla USA, Inc.Distributed Nationwide in the USAOfficial notice →
  7. 2024-05-01
  8. US
    Drugs & medicalClass II

    Cipla USA, Inc. recalls Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP, 0.5 mg & 3mg/3mL unit-dose vials, packaged in carton containing 30…

    Short fill: Complaints received of less fill volume in respule and few drops of liquid observed in the intact pouch.

    FDA · DrugCipla USA, Inc.USA nationwide.Official notice →
  9. 2023-07-19
  10. US
    Drugs & medicalClass I

    Cipla USA, Inc. recalls Albuterol Sulfate Inhalation Aerosol, 90 mcg, 200 Metered Inhalation, net content 6.7 g canister packaged in a box, Rx only, Manufactured…

    Defective container: empty inhaler and leakage observed through the inhaler valve due to partially missing bottom seat (gasket).

    FDA · DrugCipla USA, Inc.Nationwide in the USOfficial notice →
  11. 2022-10-12
  12. US
    Drugs & medicalClass II

    CIPLA recalls Arformoterol Tartrate Inhalation Solution, 15 mcg/2mL, 2 mL Sterile Unit-Dose Vial packaged in 5 x 2 mL Sterile Unit-Dose Vials per pouch,…

    Lack of Assurance of Sterility: environmental monitoring failure.

    FDA · DrugCIPLAProduct was distributed nationwide to distributors/wholesalers who may have…Official notice →
All 20 Cipla recalls →

Other drugs & medical recalls in the United States

  1. 2024-11-20
  2. US
    Drugs & medicalClass I

    Philips Respironics, Inc. recalls Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediatric through…

    Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

    FDA · DevicePhilips Respironics, Inc.Worldwide distribution - US Nationwide and the countries of AE, AF, AR, AT,…Official notice →
  3. US
  4. US
    Drugs & medicalClass III

    The Harvard Drug Group LLC dba Major Pharmaceuticals and… recalls Hydralazine HCl Tablets, USP, 25mg, Rx only, 100 tablets per carton, Distributed by: Avet…

    Failed Impurities/Degradation Specifications; during routine stability testing for impurities.

    FDA · DrugThe Harvard Drug Group LLC dba Major Pharmaceuticals and…Nationwide in the US.Official notice →
  5. US
    Drugs & medicalClass II

    Trinity Gold Nutrition recalls Trinity Gold Nutrition, 60 Capsule, 30 day Supply, Distributed by Trinity Gold Nutrition 201 Tom Hall St. Ste. 2107, Fortmill, SC 29716,…

    Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac and phenylbutazone.

    FDA · DrugTrinity Gold NutritionNationwide within the United States; additionally Canada, England, and…Official notice →
  6. 2024-11-13
  7. US
    Drugs & medicalClass II

    Smith & Nephew, Inc. recalls Tandem Intl Bipolar Cocr Shell/UHMWPE Liner, TI-6AL-4V Retaining Ring, 28MM I.D. 46 MM O.D., REF 71324046, sterile, femoral head bipolar…

    The Bipolar assembly contains an oversized Retainer Ring.

    FDA · DeviceSmith & Nephew, Inc.International distribution to the countries of Australia, Belgium, Canada,…Official notice →
  8. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph

    There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
See all drugs & medical recalls →