Novartis Pharmaceuticals Corporation recalls Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834,…
Failed Dissolution Specifications
Read the official notice →- Date
- 2026-08-19
- Country
- United States
- Brand
- Novartis Pharmaceuticals
- Product
- Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by:…
- Classification
- Class II
- Units
- US Nationwide
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Novartis Pharmaceuticals recalls
- 2023-12-13
USNovartis Pharmaceuticals Corporation recalls SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM…
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals
- 2023-09-27
- US
Novartis Pharmaceuticals Corp. recalls SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue…
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals.
- 2022-10-05
- US
Novartis Pharmaceuticals Corporation recalls Neoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30 Soft Gelatin Capsules per carton,…
CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
- 2022-06-15
- US
Novartis Pharmaceuticals Corporation recalls Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE, packaged in a) 5 single-use containers (0.2 mL each vial)…
Failed Impurities/Degradation Specifications.
Other drugs & medical recalls in the United States
- 2026-08-19
- US
Prestige Brands Holdings recalls CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY…
Lack of assurance of sterility. The recall is due to potential contamination
- US
Shoolin Pharma Chem LLP recalls SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey…
CGMP Deviations:Noted during FDA inspection
- US
Apollo Care, LLC recalls SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO…
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
- 2026-08-12
- US
Contego Medical, Inc recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP System), REF:…
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond issue, may fail to open following sheath retraction; and if this…
FDA · DeviceContego Medical, IncUS Nationwide distribution in the states of IL, FL, NC, WI, KY, AL, VA, DE,…Official notice → - US
Freudenberg Medical, LLC recalls Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LEF
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flange contains a Large Esophageal Flange.
FDA · DeviceFreudenberg Medical, LLCUS Nationwide distribution in the states of IN, OH, AZ, WA, FL, MO, KY, IN, NY…Official notice → - US
TISSIUM SA recalls Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO2010 Software Version: N/A Product Description: In…
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may…
FDA · DeviceTISSIUM SAUS Nationwide distribution in the states of CA, FL, IL, NJ, OH, PA.Official notice →