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Teva Pharmaceuticals USA

Teva Pharmaceuticals USA Recalls

All product recalls associated with Teva Pharmaceuticals USA.

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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 2281–2300 of 4747 recalls

Clonazepam Tablets (Teva Pharmaceuticals) – Stability Failure (2018)

Failed Stability Specifications: Out-of-specification test result for water content obtained during routine stability testing.

Class IIModerate

FDASep 20, 2018Nationwide• Teva Pharmaceuticals USA

Abilify (Otsuka Pharmaceutical) – Mislabeling (2018)

Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW Abilify are mislabeled. Product name is misspelled, storage instructions are missing and contents of kits may be incorrectly labeled on the outer packaging of the co-packaged kit.

Class IIILow

FDASep 17, 2018Nationwide• Otsuka Pharmaceutical Development & Commercialization, Inc.

Robaxin-750 (Endo Pharmaceuticals) – Incorrect Instructions (2018)

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Labeling: Incorrect Instructions: Dosage information on the immediate container label incorrectly states "Two to four tablets four times daily." rather than the correct dosage of "Two tablets three times daily."

Class IHigh

FDASep 17, 2018Nationwide• Endo Pharmaceuticals, Inc.

Minivelle 0.025mg Patch (Noven) – adhesive defect (2018)

Defective Delivery System: out of specification results for shear, an attribute related to the adhesive properties of the transdermal patches.

Class IIModerate

FDASep 7, 2018Nationwide• Noven Pharmaceuticals, Inc.

Minivelle 0.1mg Patch (Noven) – adhesive defect (2018)

Defective Delivery System: out of specification results for shear, an attribute related to the adhesive properties of the transdermal patches.

Class IIModerate

FDASep 7, 2018Nationwide• Noven Pharmaceuticals, Inc.

Minivelle 0.075mg Patch (Noven) – adhesive defect (2018)

Defective Delivery System: out of specification results for shear, an attribute related to the adhesive properties of the transdermal patches.

Class IIModerate

FDASep 7, 2018Nationwide• Noven Pharmaceuticals, Inc.

Minivelle 0.05mg Patch (Noven) – adhesive defect (2018)

Defective Delivery System: out of specification results for shear, an attribute related to the adhesive properties of the transdermal patches.

Class IIModerate

FDASep 7, 2018Nationwide• Noven Pharmaceuticals, Inc.

Pramipexole ER Tablets (Par) – impurity concern (2018)

Failed impurities/degradation specifications: Finished product contain a known product impurity about current specification levels.

Class IIILow

FDASep 6, 2018Nationwide• Par Pharmaceutical, Inc.

Bupropion ER Tablets (InvaGen) – impurity issue (2018)

Failed impurities/ degradation specifications: Out-of-specification results were observed in the meta-chlorobenzoic acid impurity in batches 18 months or older from date of manufacture in the 90 count bottle size.

Class IIILow

FDASep 6, 2018Nationwide• InvaGen Pharmaceuticals, Inc.

Synjardy Tablets (Boehringer) – product contamination (2018)

Cross Contamination With Other Products:

Class IIModerate

FDASep 4, 2018Nationwide• Boehringer Ingelheim Pharmaceuticals, Inc.

Reptile Strip Lights (McLanzoo) – fire hazard (2018)

Fire/Burn Risk

This recall involves 20 inch and 30 inch All Living Things reptile strip light fixtures. These light fixtures simulate natural daylight and are attached to the top of the reptile's terrarium. The 20 inch fixture has UPC number 73725773305 and the 30 inch fixture has UPC number 73725773306 printed on the packaging.

CPSCAug 30, 2018Nationwide• Tianjin McLanzoo Pet Articles, of Tianjin, China

Furosemide Injection (SCA Pharmaceuticals) – Precipitate Presence (2018)

Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.

Class IHigh

FDAAug 27, 2018CT, IN, VA +1 more• SCA Pharmaceuticals, Inc.

Levonorgestrel Estradiol Tablets (Mylan) – Labeling Error (2018)

Labeling: Not Elsewhere Classified-Incorrect NDC and product name identified on blister packs.

Class IIILow

FDAAug 27, 2018Nationwide• Mylan Pharmaceuticals Inc.

MethylPREDNISolone Tablets (Jubilant Cadista) – Stability Failure (2018)

Failed Stability Specifications: An out-of-specification result was obtained during 18-month stability testing for assay.

Class IIILow

FDAAug 27, 2018Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Cortaid Anti-itch Cream (Valeant) – Microbial Contamination (2018)

CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.

Class IIModerate

FDAAug 24, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Cortaid Cooling Spray (Valeant) – Microbial Contamination (2018)

Class IIModerate

FDAAug 24, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Cortaid Maximum Strength Cream (Valeant) – Microbial Contamination (2018)

Class IIModerate

FDAAug 24, 2018Nationwide• Valeant Pharmaceuticals North America LLC

Confer Curve Pool Steps – Drowning Hazard (2018)

This recall involves three models of in-pool step systems with curved steps for in-ground and aboveground pools. The steps and handrails are made of gray and beige plastic. The manufacturing/date code is located on the side walls of each step. Model Product Description Manufacturing/Date Code Range #CCX-AG Confer Curve base (staircase) 4-step for aboveground pool All 2013-2018 #CCX-IG Confer Curve base (staircase) 3-step for in-ground pool All 2013-2018 #CCX-ADD Curve add-on unit for either in-ground or aboveground stairs All 2013-2018

CPSCAug 21, 2018Nationwide• Confer Plastics, of North Tonawanda, N.Y.

Thyroid Powder (Sichuan Friendly) – Ingredient Inconsistency (2018)

CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

Class IIModerate

FDAAug 21, 2018Nationwide• Sichuan Friendly Pharmaceutical Co.,Ltd.

Valsartan Tablets 320mg (Preferred Pharmaceuticals) – carcinogen impurity (2018)

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Class IIModerate

FDAAug 15, 2018AL, IN• Preferred Pharmaceuticals, Inc