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

Read the official notice →
Date
2022-08-10
Country
United States
Brand
Glenmark Pharmaceuticals
Product
Tacrolimus Ointment, 0.1%, For Dermatological Use Only, Not for Ophthalmic Use, Rx Only, a) 30 g tube, NDC 68462-534-35, b) 60 g tube, NDC…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Glenmark Pharmaceuticals recalls

  1. 2023-11-08
  2. US
    Drugs & medicalClass III

    Glenmark Pharmaceuticals Inc., USA recalls Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 5mg/6.25mg, 100-count Bottle, RX only, Manufactured by: Glenmark…

    Failed Impurities/Degradation Specifications

    FDA · DrugGlenmark Pharmaceuticals Inc., USANationwide in the USAOfficial notice →
  3. 2023-08-30
  4. 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 →
  5. 2022-08-17
  6. 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 →
  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. 2022-07-06
  12. US
All 43 Glenmark Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2022-08-10
  2. US
    Drugs & medicalClass I

    North American Diagnostics recalls SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML LDT Kits, SML…

    Various brands of SARS CoV 2 Antigen Rapid Test kits were offered for sale and distribution to consumers in the United States without marketing approval, clearance, or authorization from FDA.

    FDA · DeviceNorth American DiagnosticsWorldwide distribution - US Nationwide distribution in the states of FL, LA,…Official notice →
  3. US
    Drugs & medicalClass I

    Ultra Supplement LLC recalls SUSTANGO (Pendenadril Tytrate Blend) Capsules, 400 mg, 10-count blisters per carton, Formulated by: Male FX Labs, Bangor, ME, ASIN…

    Marketed Without an Approved NDA/ANDA: Analytical testing showed the presence of tadalafil.

    FDA · DrugUltra Supplement LLCProduct was distributed nationwide in the USA via Amazon Marketplace on…Official notice →
  4. US
    Drugs & medicalClass I

    Distributor RFR, LLC. recalls SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800)…

    Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.

    FDA · DrugDistributor RFR, LLC.Retail stores in the state of FL, Nationwide in the USA, France and Canada via…Official notice →
  5. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA Inc recalls Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30-count bottles, Rx Only, Manufactured by: Actavis…

    Failed Dissolution Specifications: below specification limits for dissolution.

    FDA · DrugTeva Pharmaceuticals USA IncNationwide in the USA and Puerto RicoOfficial notice →
  6. US
    Drugs & medicalClass II

    Tolmar, Inc. recalls Naftifine Hydrochloride Gel, USP 1%, packaged in cartons with: a) Net Wt. 90g tube (NDC 0115-1510-48), b) Net Wt. 40g tube (NDC…

    Failed Impurities/ degradation specifications: Out-of-Specification test results obtained for Unspecified Impurity Relative Retention Time

    FDA · DrugTolmar, Inc.distributed to 1 consignee in KY.Official notice →
  7. 2022-08-03
  8. US
    Drugs & medicalClass II

    Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)

    Manufacturing error that may have resulted in a cathode component being out of specification. All devices met final functional testing requirements.

    FDA · DeviceMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)US Nationwide distribution in the states of Indiana and CA.Official notice →
See all drugs & medical recalls →