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Teva Pharmaceuticals USA Inc

Teva Pharmaceuticals USA Inc Recalls

All product recalls associated with Teva Pharmaceuticals USA Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

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 5461–5480 of 25000 recalls

Matzim LA Tablets (Teva) – Dissolution Failure (2022)

Failed Dissolution Specifications: below specification limits for dissolution.

Class IIModerate

FDAJul 21, 2022Nationwide• Teva Pharmaceuticals USA Inc

Amaranth Grain Organic (Natural Grocers) – Salmonella Risk (2022)

Salmonella

Potential to be contaminated with Salmonella

Class IIModerate

FDAJul 21, 2022AZ, AR, CO +18 more• Vitamin Cottage Natural Food Markets, Inc.

EVIS EXERA III Bronchovideoscope (Aizu Olympus) – Incorrect Usage (2022)

The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.

1...272 273274275 276...1250

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FDAJul 20, 2022Nationwide• Aizu Olympus Co., Ltd. 1 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Alinity m System (Abbott Molecular) – Optical Calibration Error (2022)

Incorrect optical calibration

FDAJul 19, 2022Nationwide• Abbott Molecular, Inc.

Prednisone Tablets (Strides Pharma) – Foreign Tablet Contamination (2022)

Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets

Class IIModerate

FDAJul 19, 2022Nationwide• Strides Pharma Inc.

Irbesartan Tablets (Jubilant Cadista) – Dissolution Failure (2022)

Failed Dissolution Specifications

Class IIModerate

FDAJul 18, 2022Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Irbesartan Tablets (Jubilant Cadista) – Dissolution Failure (2022)

Failed dissolution specifications.

Class IIModerate

FDAJul 18, 2022Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Arcimoto FUV (Arcimoto) – Electrical Cable Issue (2022)

Arcimoto Inc. (Arcimoto) is recalling certain 2019-2022 FUV, 2020-2022 Roadster, Deliverator and 2021 Rapid Responder hybrid electric vehicles. The high voltage (HV) control board cover may prevent the high voltage connector from latching properly to the plug.

NHTSAJul 15, 2022Nationwide• ARCIMOTO

Aesculap Ennovate Set Screw (Aesculap) – Potential Incorrect Screw (2022)

Potential for the incorrect screw to be included in the package.

FDAJul 15, 2022GA, TX• Aesculap Implant Systems LLC

Fulvestrant Injection (Zydus) – Impurity Specification (2022)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAJul 15, 2022Nationwide• Zydus Pharmaceuticals (USA) Inc

Avant Hand Sanitizer (Aire-Master) – Water System Issue (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Common Sense Hand Sanitizer (Aire-Master) – Water Contamination (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Protect U Guard Hand Sanitizer (Aire-Master) – Water Quality Concerns (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Protect U Guard Hand Sanitizer (Aire-Master) – Manufacturing Deviation (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Organic Blueberries (Natierra) – elevated lead (2022)

Elevated levels of lead detected as a result of testing conducted by Maryland Department of Health.

Class IIModerate

FDAJul 15, 2022Nationwide• BrandStorm Inc

Avant Hand Sanitizer (Aire-Master) – Water Contamination (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Stage 2 Ophardt Hand Sanitizer (Aire-Master) – Production Flaw (2022)

CGMP Deviations: product manufactured using deionized water from a system lacking appropriate microbial control post deionization.

Class IIModerate

FDAJul 15, 2022FL, IL, IA +1 more• Aire-Master of America Inc

Aeos Robotic Digital Microscope (Aesculap) – Software Application Errors (2022)

Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:

FDAJul 14, 2022AR, IN, NE +1 more• Aesculap Implant Systems LLC

Can-Am Ryker (Can-Am) – Handlebar Stem Bolt Risk (2022)

Bombardier Recreational Products Inc. (BRP) is recalling certain 2022 Can-Am Ryker motorcycles. The handlebar stem bolt may break unexpectedly due to insufficient thread length.

NHTSAJul 13, 2022Nationwide• CAN-AM

Ready Meals Crab & Shrimp (Albertsons) – undeclared allergens (2022)

Undeclared Allergen

Undeclared allergens; fish, shellfish, egg, wheat, and soy

Class IHigh

FDAJul 13, 2022AK, CA, CO +22 more• Albertsons Companies LLC