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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

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 19241–19260 of 25002 recalls

Ethambutol Tablets (Teva) – CGMP Manufacturing Deviation (2014)

CGMP Deviations: Ethambutol Hydrochloride Tablets, USP, 400 mg were manufactured using unapproved material: the incorrect gelatin excipient than specified in the product formulation.

Class IIModerate

FDAJan 24, 2014Nationwide• Teva Pharmaceuticals USA

San Francisco Sourdough (Farm to Market) – Undeclared Wheat (2014)

Undeclared Allergen

The product label does not list wheat flour as an ingredient. Undeclared allergen.

Class IIModerate

FDAJan 18, 2014IN, KS, MO• Farm To Market Bread Co Inc

Panko Bread Crumbs (Braum's) – Undeclared Milk (2014)

Undeclared Milk

1...961 962963964 965...1251

Page 963 of 1251Next

contains undeclared milk

Class IHigh

FDAJan 17, 2014AR, KS, MO +2 more• Braum's Ice Cream and Dairy

Bathroom Medicine Cabinets (RSI) – Injury Hazard (2014)

This recall involves four models of Glacier Bay®-branded bathroom medicine cabinets, manufactured between July 15, 2013 and October 10, 2013. They have a mirrored door, two adjustable and two fixed interior shelves. Some models have exterior display side shelves. They were sold in 21, 23 and 30-inch widths and in three finishes: cognac, java and white. "VOC" and the manufacture date are stamped on the exterior of the cabinet's back panel. The models below are included in this recall. The model and SKU number appear on the product's box. Model SKU Number Product Description S2327OS-ACO 1000004766 23" Swing Med Cab Open Side Cognac S3027OS-ACO 1000004797 30" Swing Med Cab Open Sides Cognac S2127C-JAV 1000004819 21" Curved Swing Med Cab Java S2127C-WHT 1000004822 21" Curved Swing Med Cab White

CPSCJan 16, 2014Nationwide• RSI Home Products, of Anaheim, Calif.

ROHTO Dry Eye Drops (Mentholatum) – sterility concern (2014)

Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto Arctic, Rohto Ice, Rohto Hydra, Rohto Relief and Rohto Cool eye drops, due to concerns related to the quality assurance of sterility controls.

Class IIModerate

FDAJan 16, 2014Nationwide• The Mentholatum Co.

Aston Martin V8 Vantage S (Aston Martin) – Accelerator Issue (2014)

Aston Martin Lagonda of North America (Aston Martin) is recalling certain model year 2008-2014 DB9 and V8 Vantage, 2009-2012 DBS, 2010-2012 Rapide, 2014 Rapide S, 2011-2012 V12 Vantage, 2011-2014 V8 Vantage S and 2012 Virage vehicles. Due to a manufacturing error, the accelerator pedal arm may break.

NHTSAJan 16, 2014Nationwide• ASTON MARTIN

ROHTO Redness Relief Ice (Mentholatum) – sterility concern (2014)

Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto Arctic, Rohto Ice, Rohto Hydra, Rohto Relief and Rohto Cool eye drops, due to concerns related to the quality assurance of sterility controls.

Class IIModerate

FDAJan 16, 2014Nationwide• The Mentholatum Co.

ROHTO Cooling Eye Drops (Mentholatum) – sterility concern (2014)

Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto Arctic, Rohto Ice, Rohto Hydra, Rohto Relief and Rohto Cool eye drops, due to concerns related to the quality assurance of sterility controls.

Class IIModerate

FDAJan 16, 2014Nationwide• The Mentholatum Co.

ROHTO Redness Relief Arctic (Mentholatum) – sterility concern (2014)

Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto Arctic, Rohto Ice, Rohto Hydra, Rohto Relief and Rohto Cool eye drops, due to concerns related to the quality assurance of sterility controls.

Class IIModerate

FDAJan 16, 2014Nationwide• The Mentholatum Co.

ROHTO Redness Relief (Mentholatum) – sterility concern (2014)

Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto Arctic, Rohto Ice, Rohto Hydra, Rohto Relief and Rohto Cool eye drops, due to concerns related to the quality assurance of sterility controls.

Class IIModerate

FDAJan 16, 2014Nationwide• The Mentholatum Co.

Hydraulic Bicycle Brakes (SRAM) – injury risk (2014)

The recalled bicycle brake models include SB Red Hydraulic Road Disc, SB Red Hydraulic Road Rim, SB 700 Hydraulic Road Disc and SB 700 Hydraulic Road Rim, used as either front or rear brakes. The SB RED brake lever is labeled "RED" on the body of the lever assembly. The SB 700 brake lever is labeled "S-Series" on the body of the lever assembly. The serial numbers for the recalled brakes have the digit "3" as the fourth digit of the serial number. The serial number can be found on the bottom of the caliper body. The brakes were sold as aftermarket products and as original equipment on the following bicycle brands and models: Brand Name Model Name ASI Fuji Altamira CX 1.1 Cannondale Super X Hi-Mod Black Inc. Diamondback Steilacoom RCX Carbon Pro Disc Felt Bicycles F2x Z2 Red Z3 Red Jamis Supernova Team Kona Super Jake Norco Threshold C1 Threshold SL Orbea Avan M-LTD Specialized Bicycles Crux Elite Carbon Disc Rival Crux Elite Evo Carbon Disc Crux Expert Carbon Disc Red Crux Pro Race Carbon Disc Red Crux Sport E5 Disc Apex Roubaix SL4 Elite Rival HRR C2 Roubaix SL4 Sport Disc SRAM C2 Ruby Elite Rival HRR S-works Crux Carbon Disc Red S-works Roubaix SL4 Disc Red S-works Tarmac SL4 Red HRR X2 S-works Venge Red HRR X2 Tarmac SL4 Elite Rival HRR M2 Venge Elite Rival HRR M2 Volagi Liscio 2 Giant Bicycles Revolt 0 TCX ADV 0 TCX ADV 1 TCX SLR 1 BRAVA SLR 0 Trek Bicycles Crockett 7

CPSCJan 14, 2014Nationwide• SRAM, LLC, of Chicago, Ill.

Atlantic Salmon Stix (Hannaford Bros) – listeria risk (2014)

Potential for Listeria monocytogenes contamination.

FDAJan 14, 2014ME, MA, NH +2 more• Delhaize America (Hannaford Bros)

Levothyroxine Sodium Tablets (Mylan) – subpotent medication (2014)

Subpotent Drug: Assay results obtained during stability testing for Levothyroxine Sodium Tablets, USP were below specification.

Class IIModerate

FDAJan 14, 2014Nationwide• Mylan Pharmaceuticals Inc.

Baby's Relief Cream (Dermamedics) – Unapproved Drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.

Post Procedure Cream (Dermamedics) – Unapproved Drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.

Complexion Repair Emulsion (Dermamedics) – unapproved drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.

Calm and Correct Serum (Dermamedics) – unapproved drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.

Calm and Correct Cream (Dermamedics) – unapproved drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.

Post Procedure Cream (Dermamedics) – unapproved drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.

Calm & Correct Cream (Dermamedics) – unapproved drug (2014)

Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.

Class IIModerate

FDAJan 10, 2014Nationwide• Dermamedics, L.L.C.