FoodJan 15, 2020
TFI Holding dba Grey Ghost Bakery GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT recall — FDA F-0559-2020
The product contains undeclared sulfites.
Class IIFDA: OngoingTFI Holding dba Grey Ghost Bakery
Latest records
Latest recalls — page 1098
The newest recall records with useful source details are listed here.
DrugJan 15, 2020
Appco Pharma Ranitidine Capsules 150 mg, (a) 60 count bottles (NDC 62559-690-60) , (b) 500 recall — FDA D-0649-2020
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Class IIFDA: TerminatedAppco Pharma LLC
DrugJan 15, 2020
Idelle Labs SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net Wt recall — FDA D-0786-2020
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Class IIIFDA: TerminatedIdelle Labs
DrugJan 15, 2020
Lupin Pharmaceuticals Blisovi Fe 1.5/30 recall — FDA D-0638-2020
Failed Tablet/Capsule Specifications: Complaints related to crumbling of tablets when popped out of the blister pack.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugJan 15, 2020
Idelle Labs SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant & recall — FDA D-0784-2020
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Class IIIFDA: TerminatedIdelle Labs
DrugJan 15, 2020
Idelle Labs SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net Wt recall — FDA D-0785-2020
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Class IIIFDA: TerminatedIdelle Labs
DrugJan 15, 2020
Appco Pharma Ranitidine Capsules 300 mg, 30 count bottles recall — FDA D-0648-2020
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Class IIFDA: TerminatedAppco Pharma LLC
DrugJan 15, 2020
Idelle Labs SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net recall — FDA D-0783-2020
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Class IIIFDA: TerminatedIdelle Labs
VehicleJan 13, 2020
Toyota Motor Engineering & Manufacturing fuel pump recall — NHTSA campaign 20V012000
Toyota Motor Engineering & Manufacturing (Toyota) recalled certain 2018-2019 4Runner, Highlander, Camry, Land Cruiser, Sequoia, Sienna, Tacoma and Tundra, and Lexus RC 300, RC 350, GS 350,…
fuel pumpToyota Motor Engineering & Manufacturing
Medical DeviceJan 8, 2020
Roche Diabetes Care Blood Glucose Monitoring System, Model Number 08453071001 ACCU-CHEK recall — FDA Z-0750-2020
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Class IIFDA: TerminatedRoche Diabetes Care, Inc.
Medical DeviceJan 8, 2020
Deerfield Imaging iMRX MRI and Angiography System, part number 10094137 and 10094141, a recall — FDA Z-0762-2020
There is a potential hardware error for the iMRX System with a generator A100. A tolerance issue in the power supply of the generator control above a specific value may cause generator A100…
Class IIFDA: TerminatedDeerfield Imaging, Inc.
Medical DeviceJan 8, 2020
Medtronic Navigation, Inc.-Littleton O-arm" O2 Imaging System, Product Number/CFN recall — FDA Z-0767-2020
Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems, Medtronic has determined that the gantry tractor motor drive belt may loosen over an extended number of uses at…
Class IIFDA: TerminatedMedtronic Navigation, Inc.-Littleton
Medical DeviceJan 8, 2020
Roche Diabetes Care Blood Glucose Monitoring System, Model Number 07400942001 ACCU-CHEK recall — FDA Z-0749-2020
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Class IIFDA: TerminatedRoche Diabetes Care, Inc.
Medical DeviceJan 8, 2020
Roche Diabetes Care Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK recall — FDA Z-0747-2020
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Class IIFDA: TerminatedRoche Diabetes Care, Inc.
Medical DeviceJan 8, 2020
Nucletron BV There is a complaint regarding internal check cable guide mechanism failure for recall — FDA Z-0772-2020
A component failure may lead to treatment interruption or incorrect source positioning.
Class IIFDA: TerminatedNucletron BV
Medical DeviceJan 8, 2020
Villa Sistemi Medicali S.P.A Apollo, Model Numbers 9784100231, 9784120131, 9784130131 recall — FDA Z-0764-2020
An amendment to the IFU and Service Manual is being issued to prescribe the replacement of the angulation chain after 8 years of service of the of the unit. After testing, it was found that…
Class IIFDA: OngoingVilla Sistemi Medicali S.P.A.
Medical DeviceJan 8, 2020
Roche Diabetes Care Blood Glucose Monitoring System, Model Number 07400926001 ACCU-CHEK recall — FDA Z-0748-2020
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Class IIFDA: TerminatedRoche Diabetes Care, Inc.
Medical DeviceJan 8, 2020
STANLEY BLACK & DECKER The products involved are DeWALT laser distance measurers, model recall — FDA Z-0681-2020
The products are labeled as Class II lasers. However, the level of laser radiation emitted by the distributed products may exceed the limit (1 mW) established for Class II lasers. These…
Class IIFDA: OngoingSTANLEY BLACK & DECKER Inc.
Medical DeviceJan 8, 2020
Medela Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224 recall — FDA Z-0773-2020
Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging.
Class IIFDA: TerminatedMedela Inc.
Medical DeviceJan 8, 2020
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact recall — FDA Z-0771-2020
The electromagnetic noise exceeded the upper limit of the Electromagnetic Compatibility Standard (EMC: IEC 60601-1-2)
Class IIIFDA: TerminatedNidek, Inc.
Medical DeviceJan 8, 2020
Roche Diabetes Care Blood Glucose Monitoring System, Model Number 08313202001 ACCU CHEK recall — FDA Z-0752-2020
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Class IIFDA: TerminatedRoche Diabetes Care, Inc.
Medical DeviceJan 8, 2020
Roche Diabetes Care Blood Glucose Monitoring System, Model Number 08453063001 ACCU-CHEK recall — FDA Z-0751-2020
Potential power issues with the Accu-Chek Guide Blood Glucose Monitoring System.
Class IIFDA: TerminatedRoche Diabetes Care, Inc.
Medical DeviceJan 8, 2020
Villa Sistemi Medicali S.P.A Apollo DRF, Model Number 9784220831 - Product Usage: The remote recall — FDA Z-0765-2020
An amendment to the IFU and Service Manual is being issued to prescribe the replacement of the angulation chain after 8 years of service of the of the unit. After testing, it was found that…
Class IIFDA: OngoingVilla Sistemi Medicali S.P.A.
Medical DeviceJan 8, 2020
Villa Sistemi Medicali S.P.A Apollo EZ, Model Number 9784152036 - Product Usage: The Apollo recall — FDA Z-0766-2020
An amendment to the IFU and Service Manual is being issued to prescribe the replacement of the angulation chain after 8 years of service of the of the unit. After testing, it was found that…
Class IIFDA: OngoingVilla Sistemi Medicali S.P.A.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026180 records · 4 categoriesSeptember 2026363 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