DrugNov 24, 2021
Cartia XT recall — FDA D-0232-2022
Labelling: Incorrect Exp. Date
Class IIFDA: TerminatedTeva Pharmaceuticals USA
Latest records
Latest recalls — page 798
The newest recall records with useful source details are listed here.
DrugNov 24, 2021
Bayer Healthcare Pharmaceuticals Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY NET WT133g recall — FDA D-0252-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, labeled as (a) Product of recall — FDA D-0243-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) recall — FDA D-0254-2022
cGMP Deviations: LOTRIMIN AF (Tolnaftate 1%) manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Bayer Healthcare Pharmaceuticals LOTRIMIN AF (Miconazole nitrate 2%) Jock Itch Powder Spray recall — FDA D-0237-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can, Dist by: Bayer recall — FDA D-0250-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) recall — FDA D-0240-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Bayer Healthcare Pharmaceuticals LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray recall — FDA D-0246-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) recall — FDA D-0239-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) recall — FDA D-0249-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Bayer Healthcare Pharmaceuticals LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray recall — FDA D-0236-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Bayer Healthcare Pharmaceuticals LOTRIMIN AF, (Miconazole nitrate 2%), Jock Itch, Powder recall — FDA D-0247-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can, labeled as (a) UPC recall — FDA D-0242-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Class IIFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, Labeled as (a) Product of recall — FDA D-0251-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
DrugNov 24, 2021
Bayer Healthcare Pharmaceuticals Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) recall — FDA D-0253-2022
Chemical Contamination: presence of benzene
Class IFDA: TerminatedBayer Healthcare Pharmaceuticals Inc.
VehicleNov 24, 2021
Chrysler curtain recall — NHTSA campaign 21V925000
Chrysler (FCA US, LLC) is recalling certain 2021-2022 Ram 2500, Ram 3500, and 2021 Ram 1500 Classic pickup trucks. The side air bag inflatable curtain (SABIC) assemblies may have been…
curtainChrysler (FCA US, LLC)
VehicleNov 23, 2021
Toyota Motor Engineering & Manufacturing hydraulic power assist system recall — NHTSA campaign 21V920000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2008-2022 Sequoia and 2007-2021 Tundra vehicles. The power steering gear assembly may have been manufactured…
hydraulic power assist systemToyota Motor Engineering & Manufacturing
VehicleNov 23, 2021
Ford caliper recall — NHTSA campaign 21V922000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco Sport and Escape vehicles. The rear brake linings may have been manufactured incorrectly, which can affect braking…
caliperFord Motor Company
VehicleNov 23, 2021
Chrysler display function recall — NHTSA campaign 21V918000
Chrysler (FCA US, LLC) is recalling certain 2021 Ram 1500 pickup trucks. The Trailer Reverse Steering Control Module (TRSCM) may prevent the rearview image from displaying. As such, these…
display functionChrysler (FCA US, LLC)
VehicleNov 22, 2021
Nissan trailer hitch recall — NHTSA campaign 21V917000
Nissan North America, Inc. (Nissan) is recalling certain 2022 Frontier Crew Cab Long Bed trucks. The tow hitch was not installed, compromising the structural integrity of the fuel tank in…
trailer hitchNissan North America, Inc.
VehicleNov 21, 2021
Model Y suspension recall — NHTSA campaign 21V912000
Tesla, Inc. (Tesla) is recalling certain 2020-2022 Model Y vehicles. The front and rear suspension knuckles may fracture, causing the suspension links to separate.
suspensionTesla, Inc.
VehicleNov 18, 2021
Honda retractor recall — NHTSA campaign 21V900000
Honda (American Honda Motor Co.) is recalling certain 2021 Accord Sedan, Accord Hybrid, CR-V, Ridgeline, 2022 Insight and CR-V Hybrid vehicles. The automatic locking retractor on the…
retractorHonda (American Honda Motor Co.)
Medical DeviceNov 17, 2021
Covidien Emprint Ablation Catheter with Thermosphere Technology Bronchoscopic Ablation, CFN recall — FDA Z-0210-2022
The firm identified an error in the device temperature monitoring circuitry which is designed to interrupt energy delivery in the event of a primary cooling system failure. Use of an…
Class IIFDA: TerminatedCovidien LLC
Medical DeviceNov 17, 2021
Z-Medica QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding recall — FDA Z-0211-2022
Lack of Packaging seal integrity may result in a sterile barrier breach.
Class IIFDA: TerminatedZ-Medica, LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories