Glenmark Pharmaceuticals Inc., USA recalls Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm…
Defective Container: Firm received complaints of broken tube at the seal.
Read the official notice →- Date
- 2024-10-09
- Country
- United States
- Brand
- Glenmark Pharmaceuticals
- Product
- Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC…
- Classification
- Class III
- Units
- Nationwide in the US.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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
- 2025-01-01
USGlenmark Pharmaceuticals Inc., USA recalls chlorproMAZINE Hydrochloride Tablets, USP, 10mg, 100-count bottle, RX only, Manufactured for: Glenmark Pharmaceuticals Inc.,…
CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were found to be failing per current FDA recommended limit.
- 2024-12-11
- US
Glenmark Pharmaceuticals Inc., USA recalls Diltiazem Hydrochloride Extended-Release Capsules, USP 90mg, Twice-a-Day Dosage, Rx Only, 100 Capsules per bottle, Mfd for:…
cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.
- 2024-10-09
- US
Glenmark Pharmaceuticals Inc., USA recalls Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray, 665 mcg/25 mcg per spray, 240 Metered…
Defective Delivery System: The dip tube is clogged causing the spray not to work.
- 2024-10-02
- US
Glenmark Pharmaceuticals Inc., USA recalls Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513,…
Subpotent Drug
FDA · DrugGlenmark Pharmaceuticals Inc., USAProduct was distributed nationwide within the United States.Official notice → - 2024-09-04
- US
Glenmark Pharmaceuticals Inc., USA recalls Indomethacin Extended-Release Capsules, USP, 75 mg, packaged in a) 60-count bottle (NDC 68462-325-60) and b) 90-count bottle…
Failed Dissolution Specifications: below specification results
- 2024-08-07
- US
Other drugs & medical recalls in the United States
- 2024-10-09
- US
Glenmark Pharmaceuticals Inc., USA recalls Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray, 665 mcg/25 mcg per spray, 240 Metered…
Defective Delivery System: The dip tube is clogged causing the spray not to work.
- US
Gilead Sciences, Inc. recalls Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA…
Presence of Particulate Matter: Presence of glass particle.
- US
Supercore Products Group Inc. recalls Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
FDA · DrugSupercore Products Group Inc.Nationwide US (2014), Israel (2), Canada (12), Republic of Kosovo (1),…Official notice → - US
Nivagen Pharmaceuticals Inc recalls Atorvastatin Calcium Tablets, USP, 40mg, Rx only, 1000 Tablets per bottle, Manufactured for: Nivagen Pharmaceuticals, Inc.…
Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.
- 2024-10-02
- US
Cardinal Health 200, LLC recalls (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti-Reflux Valve, 12 Fr/Ch (4.0 mm) x 48 in. (122 cm), Model #8888266114,…
The firm received reports of breakage in the Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made.
FDA · DeviceCardinal Health 200, LLCDistribution was nationwide, including Puerto Rico and Guam. There was also…Official notice → - US
Dr Franz Koehler Chemie Gmbh recalls Custodiol HTK Solution, 500ml bottle. 10 per carton.
Potential for particles to be present in solution.
FDA · DeviceDr Franz Koehler Chemie GmbhUS Nationwide distribution in the state of North Carolina.Official notice →