Recall Atlas
Drugs & medicalClass III

SUN PHARMACEUTICAL INDUSTRIES INC recalls Bupropion Hydrochloride Extended-Release Tablets USP (SR), 150 mg, 60 tablets bottle, Rx Only, Distributed by: Sun…

Failed Dissolution Specifications

Read the official notice →
Date
2023-10-25
Country
United States
Brand
Sun Pharmaceutical Industries
Product
Bupropion Hydrochloride Extended-Release Tablets USP (SR), 150 mg, 60 tablets bottle, Rx Only, Distributed by: Sun Pharmaceutical…
Classification
Class III
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Sun Pharmaceutical Industries recalls

  1. 2023-12-20
  2. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Liothyronine Sodium Tablets, USP 5 mcg, 100-count bottle, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc.…

    Failed Impurities/Degradation Specifications

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwideOfficial notice →
  3. 2023-12-13
  4. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls buPROPion Hydrochloride Extended-Release Tablets, USP (SR) 200 mg, 60 Tablets bottle, Distributed by: Sun Pharmaceutical…

    Failed Dissolution Specifications

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwideOfficial notice →
  5. 2023-11-08
  6. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Liothyronine Sodium Tablets, USP, 5 mcg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries,…

    Failed Impurities/Degradation Specifications.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide within the United StatesOfficial notice →
  7. 2023-09-27
  8. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)), Rx only,…

    Subpotent: Out of Specification result observed for low assay

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide wide in the USAOfficial notice →
  9. 2023-08-16
  10. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey…

    Out of Specification result observed in content uniformity testing

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
  11. 2023-08-02
  12. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New…

    Presence of Foreign Substance: Metal embedded in a tablet.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwideOfficial notice →
All 57 Sun Pharmaceutical Industries recalls →

Other drugs & medical recalls in the United States

  1. 2023-10-25
  2. US
    Drugs & medicalClass I

    VistaPharm LLC recalls Sucralfate Oral Suspension, 1g per 10mL, 16 oz (414 mL) PET bottle (12 bottles per case), Rx Only, Manufactured and Distributed by:…

    Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.

    FDA · DrugVistaPharm LLCUSA NationwideOfficial notice →
  3. US
    Drugs & medicalClass I

    Church & Dwight Inc recalls TheraBreath for Kids! Oral Rinse, sodium fluoride 0.05% (0.02% w/v fluoride ion), 16 fl. oz. 473 mL bottles, Strawberry Splash, UPC 6…

    Microbial contamination of Non-Sterile Product; presence of yeast identified as Candida parapsilosis

    FDA · DrugChurch & Dwight IncNationwide in the USOfficial notice →
  4. US
    Drugs & medicalClass II

    Dollar Tree Distribution, Inc. recalls Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail stores.

    CGMP Deviations: OTC products were stored outside of labeled temperature requirements.

    FDA · DrugDollar Tree Distribution, Inc.Nationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass III

    Imprimis NJOF, LLC recalls MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution Drops 1% - 0.5% - 2.5% - 0.5%, 5mL bottle,…

    Subpotent: Out of Specification result observed for Ketorolac assay levels, below the 90.0-110.0% of label claim.

    FDA · DrugImprimis NJOF, LLCProduct was distributed to physician's offices nationwide.Official notice →
  6. 2023-10-18
  7. US
    Drugs & medicalClass II

    Becton Dickinson & Co. recalls BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023

    Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.

    FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution.Official notice →
  8. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls THUNDERBEAT, 5MM, 35CM, Front-actuated Grip Type S. Model: TB-0535FCS Indicated for open, laparoscopic (including…

    Thunderbeats blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position may result in prolonged surgery

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution.Official notice →
See all drugs & medical recalls →