Drugs & medicalClass II

Dr. Reddy's Laboratories, Inc. recalls Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle…

CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.

Read the official notice →
Date
2021-10-27
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle within a…
Classification
Class II
Units
Nationwide in the USA
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Dr. Reddy's Laboratories recalls

  1. 2022-03-02
  2. US
  3. 2022-01-26
  4. US
  5. US
  6. 2021-12-15
  7. US
  8. 2021-11-10
  9. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, 500 count bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories…

    Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in…

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

    Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 count (NDC 43598-743-30), b) 90 count (NDC 43598-743-90)…

    Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USOfficial notice →
All 35 Dr. Reddy's Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2021-10-27
  2. US
    Drugs & medicalClass I

    Smiths Medical ASD Inc. recalls CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L…

    Specific Pumps may exhibit intermittent performance in the AILD (Air in Line Detector) function. If an AILD does not sufficiently discern fluid from air in line, an air in line event may not be recognized by the pump…

    FDA · DeviceSmiths Medical ASD Inc.Distribution to European countries: BE, BH, CH, DE, DK, ES, FI, FR, GB, IT,…Official notice →
  3. US
    Drugs & medicalClass I

    Datascope Corp. recalls Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) with the below…

    A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to meet the minimum runtime requirement per Getinge internal Product Specification. These nonconforming batteries were inadvertently released to…

    FDA · DeviceDatascope Corp.Worldwide distribution. US nationwide, Australia, Brazil, Bahrain, Belgium,…Official notice →
  4. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Imipramine Pamoate Capsules 125 mg, 30-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202…

    Out of specification result observed in a dissolution test at the 9-month long term stability time point.

    FDA · DrugLupin Pharmaceuticals Inc.Distributed Nationwide in the USA.Official notice →
  5. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA recalls AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC…

    Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

    FDA · DrugTeva Pharmaceuticals USAUSA NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    American Health Packaging recalls GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only,…

    Failed Dissolution Specifications: results were above specification.

    FDA · DrugAmerican Health PackagingNationwide within the USAOfficial notice →
  7. US
    Drugs & medicalClass II

    Piramal Critical Care, Inc. recalls Rocuronium Bromide Injection 50mg/5 mL, 5mL Multi-Dose Vial, Rx only, Manufactured for: Piramal Critical Care, Bethlehem, PA 18017,…

    Labeling: Label Lacks Warning or Rx Legend: Finished product did not include the statement on the flip cap vial, "WARNING: PARALYZING AGENT"

    FDA · DrugPiramal Critical Care, Inc.Nationwide within the United StatesOfficial notice →
See all drugs & medical recalls →