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Mylan Pharmaceuticals Inc.

Mylan Pharmaceuticals Inc. Recalls

All product recalls associated with Mylan Pharmaceuticals Inc..

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Recall Summary

Total Recalls

1000

Past Year

303

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 2761–2780 of 4747 recalls

Mirtazapine Tablets (Mylan) – Foreign Tablet Risk (2017)

Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet in bottle

Class IIModerate

FDAJan 19, 2017Nationwide• Mylan Pharmaceuticals Inc.

Dexamethasone Elixir (Qualitest) – Impurity Specifications (2017)

Failed Impurities/ Degradation Specifications

Class IIILow

FDAJan 16, 2017Nationwide• Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Carbidopa and Levodopa Tablets (Sun Pharma) – Failed Dissolution (2017)

Failed Dissolution Specifications

Class II

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Page 139 of 238Next

Moderate

FDAJan 12, 2017Nationwide• Sun Pharmaceutical Industries, Inc.

Snowmobiles (Arctic Cat) – Fire Risk (2017)

Fire/Burn Risk

The recall involves model year 2007, 2008, and 2009 Arctic Cat snowmobiles, including F models, Jaguar and Jaguar Z1 1100 models, Bearcat Z1 XT models, T500 and T570 models, TZ1 and TZ1 Turbo models, and Z1 1100 and Z1 1100 Turbo models. These snowmobiles were produced in a variety of color combinations. "Arctic Cat" is printed on the sides of the vehicle and on the back snow-flap area. The model name is on the side of the vehicle. The model number is printed in the owner's manual.

CPSCJan 11, 2017Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.

Alfuzosin Tablets (Sun Pharma) – Foreign Substance (2017)

Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.

Class IIModerate

FDAJan 5, 2017Nationwide• Sun Pharmaceutical Industries, Inc.

Alaska Salmon Bites (Authentic Alaska) – Undeclared soy (2016)

Fire/Burn Risk

Alaska Salmon Bites (jerky), Spicy Fireweed Honey flavor is recalled due to undeclared soy. Product contains undeclared soy sauce from the ingredient Tamari sauce.

Class IIModerate

FDADec 23, 2016CA, IN, MD• Authentic Alaska

Alaska Salmon Bites (Authentic Alaska) – Undeclared soy (2016)

Undeclared Soy

Alaska Salmon Bites (jerky), Rhubarb & Raspberries flavor is recalled due to undeclared soy. Product contains undeclared soy sauce from the ingredient Tamari sauce.

Class IIModerate

FDADec 23, 2016CA, IN, MD• Authentic Alaska

Temazepam Capsules (Qualitest) – Failed Stability (2016)

Failed Stability Specifications

Class IIILow

FDADec 22, 2016Nationwide• Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Southwest Chipotle Seasoning (J M Exotic) – Salmonella Risk (2016)

Salmonella

Spice blends were manufactured using dried buttermilk which was subsequently recalled due to positive Salmonella results on environmental sampling.

Class IHigh

FDADec 21, 2016AL, SC• J M Exotic Foods Inc

Ranch Dressing (Wood Farms) – Salmonella Risk (2016)

Salmonella

Spice blends were manufactured using dried buttermilk which was subsequently recalled due to positive Salmonella results on environmental sampling.

Class IHigh

FDADec 21, 2016AL, SC• J M Exotic Foods Inc

Amoxicillin Suspension (Teva) – Subpotency Concern (2016)

Subpotency: due to a low, out of specification test result for assay during stability testing.

Class IIModerate

FDADec 21, 2016Nationwide• Teva Pharmaceuticals USA

Bupropion Extended-Release 200mg (Sun) – Dissolution Failure (2016)

Failed Dissolution Specifications; 18 month stability time point

Class IIILow

FDADec 20, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Bupropion Extended-Release 150mg (Sun) – Dissolution Failure (2016)

Failed Dissolution Specifications; 18 month stability time point

Class IIILow

FDADec 20, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Extra-Virt Plus DHA Softgel (Virtus Pharmaceuticals) – API Import Alert (2016)

cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.

Class IIILow

FDADec 12, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

VirtPrex Prenatal Tablets (Virtus Pharmaceuticals) – API Import Alert (2016)

cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.

Class IIILow

FDADec 12, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Rabeprazole Sodium Tablets (Amneal) – Failed Dissolution (2016)

Failed Dissolution Specifications

Class IIModerate

FDADec 12, 2016Nationwide• Amneal Pharmaceuticals LLC

Virt-Select Prenatal Softgels (Virtus Pharmaceuticals) – API Import Alert (2016)

cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.

Class IIILow

FDADec 12, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Virt-Advance Prenatal Softgels (Virtus Pharmaceuticals) – API Import Alert (2016)

cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.

Class IIILow

FDADec 12, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

INOVA Easy Pad (Cipher Pharmaceuticals) – Subpotent Formulation (2016)

Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial Stability testing showed variation within the lot outside of product specifications.

Class IIILow

FDADec 6, 2016AZ, CO, OH• Cipher Pharmaceuticals US LLC

Risedronate Sodium Tablets (Teva) – Failed Dissolution (2016)

Failed Dissolution Specifications

Class IIILow

FDADec 1, 2016Nationwide• Teva Pharmaceuticals USA