Drugs & medicalClass II

Glenmark Pharmaceuticals Inc., USA recalls Desmopressin Acetate Tablets, 0.2 mg, 100-count bottles, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141,…

CGMP Deviations

Read the official notice →
Date
2022-07-06
Country
United States
Brand
Glenmark Pharmaceuticals
Product
Desmopressin Acetate Tablets, 0.2 mg, 100-count bottles, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by:…
Classification
Class II
Units
One sole distributor in TX
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Glenmark Pharmaceuticals recalls

  1. 2023-08-30
  2. US
    Drugs & medicalClass III

    Glenmark Pharmaceuticals Inc., USA recalls Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg, 100-count Bottle, Rx only, Manufactured by:…

    Subpotent: Out of Specification for Assay Test at the 3-month time point.

    FDA · DrugGlenmark Pharmaceuticals Inc., USAnationwide in the U.S.Official notice →
  3. 2022-08-17
  4. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals…

    Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

    FDA · DrugGlenmark Pharmaceuticals Inc., USAnationwideOfficial notice →
  5. 2022-08-10
  6. US
    Drugs & medicalClass III

    Glenmark Pharmaceuticals Inc., USA recalls Tacrolimus Ointment, 0.1%, For Dermatological Use Only, Not for Ophthalmic Use, Rx Only, a) 30 g tube, NDC 68462-534-35, b)…

    Defective Container: Tube split from side seam

    FDA · DrugGlenmark Pharmaceuticals Inc., USANationwide in the USAOfficial notice →
  7. 2022-07-27
  8. US
    Drugs & medicalClass III

    Glenmark Pharmaceuticals Inc., USA recalls Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark…

    Failed Tablet/Capsule Specification : Capsule breakage

    FDA · DrugGlenmark Pharmaceuticals Inc., USAUSA NationwideOfficial notice →
  9. 2022-07-13
  10. US
  11. 2022-05-04
  12. US
All 43 Glenmark Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2022-07-06
  2. US
    Drugs & medicalClass II

    GE Healthcare, LLC recalls Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019

    Backup batteries can fail earlier than their estimated life.

    FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide and the countries of Algeria,…Official notice →
  3. US
    Drugs & medicalClass II

    Microgenics Corporation recalls QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3 QMS TACROLIMUS CAL…

    Due to QMS Tacrolimus Calibrator recovering between 82 to 94% of their target values, resulting in over-quantitation in tacrolimus patient result values when used with the QMS Tacrolimus Immunoassay.

    FDA · DeviceMicrogenics CorporationU.S.: AL, AZ, CA, DC, FL, IA, ID, IL, KY, LA, MA, NE, NJ, NM, OH, OK, PA, SC,…Official notice →
  4. US
    Drugs & medicalClass II

    Akorn, Inc. recalls Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL…

    Defective container: defect prevents product from dispensing as intended.

    FDA · DrugAkorn, Inc.Nationwide USAOfficial notice →
  5. US
    Drugs & medicalClass II

    Akorn, Inc. recalls Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC.,…

    Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.

    FDA · DrugAkorn, Inc.Nationwide in the U.S.Official notice →
  6. US
    Drugs & medicalClass II

    Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for…

    Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.

    FDA · DrugNoven Pharmaceuticals IncDistributed Nationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass I

    Akcea Therapeutics, Inc. recalls Tegsedi (inotersen) Injection 284 mg/1.5 mL, Rx Only, Sterile solution for Subcutaneous Use, 4 prefilled syringes, each containing 284…

    Superpotent: High Out of specification (OOS) test result for percent label claim (%LC).

    FDA · DrugAkcea Therapeutics, Inc.KY, USAOfficial notice →
See all drugs & medical recalls →