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.
Monthly breakdown
2021 recalls by month
Select a month to review the recall records reported during that period.
December 2021194 records · 4 categoriesNovember 2021210 records · 4 categoriesOctober 2021342 records · 4 categoriesSeptember 2021300 records · 4 categoriesAugust 2021279 records · 4 categoriesJuly 2021251 records · 4 categoriesJune 2021361 records · 4 categoriesMay 2021226 records · 4 categoriesApril 2021279 records · 4 categoriesMarch 2021241 records · 4 categoriesFebruary 2021320 records · 4 categoriesJanuary 2021226 records · 4 categories
2021 recalls — page 12
Records are ordered by the best available source date.
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
Medical DeviceNov 17, 2021
THERAKOS CELLEX Photopheresis Procedural Kit PRODUCT CODE: CLXUSA recall — FDA Z-0212-2022
Product was released prior to all testing being completed. If used and a drive tube leak were to occur, may cause illness or injury.
Class IIFDA: OngoingTherakos, Inc.
Medical DeviceNov 17, 2021
Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model recall — FDA Z-0213-2022
When the user presses or releases both the APC (accept) button and the Float Tabletop (panning) button at the same time, the geometry may stop reacting on movement requests (table lock-up)…
Class IIFDA: TerminatedPhilips North America LLC
Medical DeviceNov 17, 2021
Baxter Healthcare Hemodialysis Delivery System, Software Version 2.x recall — FDA Z-0215-2022
If the operator initiates therapy with a saved prescription profile and makes a change to the prescription after a disposable filter change using the Same Patient button, the system may…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 17, 2021
BioCheck T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only This recall — FDA Z-0214-2022
Immunoassay TEST Kit do not meet product shelf-life standards resulting in failed controls.
Class IIFDA: TerminatedBioCheck, Inc.
FoodNov 17, 2021
The Kroger Co Country Oven Raspberry Cake 71oz recall — FDA F-0153-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Class IIFDA: TerminatedThe Kroger Co
FoodNov 17, 2021
The Kroger Co Country Oven Yellow/Fudge Cake 48oz, single slices recall — FDA F-0146-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Class IIFDA: TerminatedThe Kroger Co
FoodNov 17, 2021
The Kroger Co Country Oven Chocolate Cake 13.5oz, 60oz, 40oz recall — FDA F-0138-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Class IIFDA: TerminatedThe Kroger Co
FoodNov 17, 2021
Simply Delicious Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack recall — FDA F-0169-2022
Almond Butter Bars contain undeclared peanuts.
Class IFDA: TerminatedSimply Delicious, Inc.
FoodNov 17, 2021
The Kroger Co Country Oven Boston Cream Cake Double Layer Cake 28oz recall — FDA F-0152-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Class IIFDA: TerminatedThe Kroger Co
About the 2021 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.