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Par Pharmaceutical, Inc.

Par Pharmaceutical, Inc. Recalls

All product recalls associated with Par Pharmaceutical, Inc..

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Recall Summary

Total Recalls

1000

Past Year

303

Class I (Serious)

34

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 2801–2820 of 4747 recalls

Travoprost Solution (Par) – Sterility Risk (2016)

Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container

Class IIModerate

FDAOct 5, 2016Nationwide• Par Pharmaceutical, Inc.

Phenobarbital Tablets (West-Ward) – Dissolution Failure (2016)

Failed Dissolution Specifications: Phenobarbital Tablets have an out of specification for dissolution at the 12 month stability time point

Class IIModerate

FDAOct 3, 2016Nationwide• West-Ward Pharmaceuticals Corp.

Prednisone Tablets (West-Ward) – Underweight Tablet (2016)

Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

1...139 140141142 143...238

Page 141 of 238Next

Class II

Moderate

FDAOct 3, 2016Nationwide• West-Ward Pharmaceutical

Gildess 24 FE (Par) – Subpotent Ethinyl Estradiol (2016)

Subpotent Drug; Ethinyl Estradiol

FDASep 27, 2016Nationwide• Par Pharmaceutical, Inc.

Gildess FE 1/20 (Par Pharmaceutical) – subpotent drug (2016)

Subpotent Drug; Ethinyl Estradiol

FDASep 27, 2016Nationwide• Par Pharmaceutical, Inc.

Gildess 1.5/30 (Par Pharmaceutical) – subpotent drug (2016)

Subpotent Drug; Ethinyl Estradiol

FDASep 27, 2016Nationwide• Par Pharmaceutical, Inc.

Gildess FE 1.5/30 (Par Pharmaceutical) – subpotent drug (2016)

Subpotent Drug; Ethinyl Estradiol

FDASep 27, 2016Nationwide• Par Pharmaceutical, Inc.

Gildess 1/20 (Par Pharmaceutical) – subpotent drug (2016)

Subpotent Drug; Ethinyl Estradiol

FDASep 27, 2016Nationwide• Par Pharmaceutical, Inc.

Paricalcitol 4mcg Capsules (Teva) – impurity specs (2016)

Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.

FDASep 22, 2016Nationwide• Teva Pharmaceuticals USA

Paricalcitol 2mcg Capsules (Teva) – impurity specs (2016)

Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.

FDASep 22, 2016Nationwide• Teva Pharmaceuticals USA

Paricalcitol 1mcg Capsules (Teva) – impurity specs (2016)

Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.

FDASep 22, 2016Nationwide• Teva Pharmaceuticals USA

mitoXANTRONE Injection (Teva) – Impurities Specification Failure (2016)

Failed Impurities/Degradation Specifications: potential failure to meet the specification for Impurity D throughout shelf-life.

FDASep 13, 2016Nationwide• Teva Pharmaceuticals USA

Desoximetasone Cream 0.25% (Taro) – Homogeneity Test Failure (2016)

Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).

Class IIModerate

FDASep 13, 2016PR• Taro Pharmaceuticals, Inc.

buPROPion Extended-release Tablets (Sun Pharma) – Failed Dissolution (2016)

Failed Dissolution Specifications

FDASep 13, 2016Nationwide• Sun Pharmaceutical Industries, Inc.

Desoximetasone Cream 0.05% (Taro) – Homogeneity Test Failure (2016)

Failed Stability Specifications: The subject lots exhibited OOS results for Homogeneity test (Moderate separation).

Class IIModerate

FDASep 13, 2016PR• Taro Pharmaceuticals, Inc.

Ondansetron HCI API (Cadila) – Microbial Contamination (2016)

Microbial Contamination of Non-Sterile Product

Class IIModerate

FDASep 9, 2016IN• Cadila Pharmaceuticals Limited

Hyoscyamine Sulfate (Virtus) – Potency Variation (2016)

Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.

FDASep 2, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Hyoscyamine Disintegrating Tablets (Virtus) – Potency Variation (2016)

Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.

FDASep 2, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Hyoscyamine Tablets (Virtus) – Potency Variation (2016)

Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.

FDASep 2, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L

Side-by-Side Utility Vehicles (Arctic Cat) – Crash Risk (2016)

This recall involves all model year 2016 Arctic Cat 700 HDX models and model year 2017 Arctic Cat 700 HDX CREW models within the vehicle identification number range of 300001 through 301280. The recalled utility vehicles have four wheels with side-by-side seating for three or six people. They were sold in a variety of colors including green, black, fire red, true timber camo and other colors. "Arctic Cat" is printed on the sides, front and rear of the utility vehicles. "HDX" is printed on the sides of the front fenders. The vehicle identification number on the 700 HDX CREW models is stamped into the upper frame tube under the rear of the cargo box.

CPSCAug 23, 2016Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.