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Key Pharmacy and Compounding Center

Key Pharmacy and Compounding Center Recalls

All product recalls associated with Key Pharmacy and Compounding Center.

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Recall Summary

Total Recalls

597

Past Year

Class I (Serious)

Most Recent

May 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 341–360 of 597 recalls

Sodium Carboxymethylcellulose Ophthalmic (Key Pharmacy) – Sterility Risk (2017)

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Class IIModerate

FDAApr 18, 2017Nationwide• Key Pharmacy and Compounding Center

Testosterone Micronized (Zizhu Pharmaceutical) – cGMP deviation (2017)

cGMP Deviations; lack of quality assurance.

Class IIModerate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Estrone Micronized (Zizhu Pharmaceutical) – cGMP deviation (2017)

cGMP Deviations; lack of quality assurance.

Class II

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Moderate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Ethinyl Estradiol Micronized (Qinhuangdao Zizhu) – Quality Assurance Issues (2017)

cGMP Deviations; lack of quality assurance.

Class IIModerate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Estradiol Non-Micronized (Qinhuangdao Zizhu) – Quality Assurance Issues (2017)

cGMP Deviations; lack of quality assurance.

Class IIModerate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Levonorgestrel Non-Micronized (Qinhuangdao Zizhu) – Quality Assurance Issues (2017)

cGMP Deviations; lack of quality assurance.

Class IIModerate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Estriol Micronized (Zizhu Pharmaceutical) – cGMP deviation (2017)

cGMP Deviations; lack of quality assurance.

Class IIModerate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Estradiol Micronized (Zizhu Pharmaceutical) – cGMP deviation (2017)

cGMP Deviations; lack of quality assurance.

Class IIModerate

FDAMar 24, 2017CO, MN, NJ +3 more• Qinhuangdao Zizhu Pharmaceutical, Co.

Isopto Carpine (Novartis) – Impurity Specification Failure (2017)

Failed Impurities/Degradation Specifications.

Class IIILow

FDAMar 22, 2017Nationwide• Novartis Pharmaceuticals Corp.

Pilocarpine Hydrochloride Solution (Novartis) – Impurity Specification Failure (2017)

Failed Impurities/Degradation Specifications.

Class IIILow

FDAMar 22, 2017Nationwide• Novartis Pharmaceuticals Corp.

Remington Gasoline Chainsaws – Fire Hazard (2016)

Fire/Burn Risk

This recall involves Remington-branded chainsaws powered by a two-cycle gasoline engine ranging in size from 42cc to 46cc and with either a 14-inch, 18-inch or 20-inch bar. The chainsaw's housing is orange and black and Remington is printed on the side of the unit and on the bar. Chainsaws included in this recall have model numbers RM4214, RM4218 and RM4620 and serial numbers 1K155XQ0198 through 1F076XQ0200; and were manufactured between November 15, 2015 and June 7, 2016. Model and serial numbers and the manufacture date are located on a white label above the rear handle. The second through fifth characters of the serial number identify the manufacturing date. The second character is the month with A = January, B = February, C = March, etc. The third and fourth characters are the day of the month. The fifth character is the last digit of the year of manufacture (e.g. C286 = March 28, 2016).

CPSCDec 15, 2016Nationwide• Zhejiang Pioneer Machinery & Electron Co., Ltd., of China

Craftsman Gasoline Chainsaws – Fire Hazard (2016)

Fire/Burn Risk

This recall involves Craftsman-branded chainsaws powered by a two-cycle gasoline engine ranging in size from 42cc to 46cc and with either a 16-inch, 18-inch or 20-inch bar. The chainsaw's housing is red and black and Craftsman is printed on the side of the unit and on the bar. Chainsaws included in the recall have model numbers 41AY427S799 316.38070, 41AY429S799 316.38090, 41AY462S799 316.38098 and 41AY469S799 316.38188, and serial numbers 1K155XQ0198 through 1F076XQ0200; and were manufactured between November 15, 2015 and June 7, 2016. Model and serial numbers and the manufacture date are located on a white label above the rear handle. The second through fifth characters of the serial number identify the manufacturing date. The second character is the month with A = January, B = February, C = March, etc. The third and fourth characters are the day of the month. The fifth character is the last digit of the year of manufacture (e.g. B196 = February 19, 2016).

CPSCDec 15, 2016Nationwide• Zhejiang Pioneer Machinery & Electron Co., Ltd., of China

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

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

Sodium Ferric Gluconate (West-Ward) – Subpotent Drug (2016)

Subpotent Drug: Product has an an out of specification in iron assay analysis found during 18 month stability testing.

Class IIILow

FDANov 17, 2016Nationwide• West-Ward Pharmaceuticals Corp.

Amoxicillin Suspension (West-Ward) – Labeling Error (2016)

Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.

Class IIILow

FDANov 4, 2016Nationwide• West-Ward Pharmaceuticals Corp.

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.

Hyoscyamine Sulfate (Virtus) – Potency Variation (2016)

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

Class IHigh

FDASep 2, 2016Nationwide• VIRTUS PHARMACEUTICALS OPCO II L