FoodNov 17, 2021
The Kroger Co Country Oven Caramel Apple Double Layer Cake 32 oz recall — FDA F-0151-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Class IIFDA: TerminatedThe Kroger Co
Latest records
Latest recalls — page 800
The newest recall records with useful source details are listed here.
FoodNov 17, 2021
The Kroger Co Country Oven Yellow/Caramel Cake Single Slices, double layer recall — FDA F-0150-2022
Downstream Recall - Possible metal fragments in starch that was used to manufacture cakes.
Class IIFDA: TerminatedThe Kroger Co
DrugNov 17, 2021
Tadalafil Tablets, USP 20 mg, 30 count bottle recall — FDA D-0231-2022
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugNov 17, 2021
Tadalafil Tablets, USP 5 mg, 30 count bottle recall — FDA D-0230-2022
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugNov 17, 2021
Cetirizine hydrochloride, 10 mg tablets, 90-count bottle recall — FDA D-0096-2022
Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets.
Class IIIFDA: TerminatedA-S Medication Solutions LLC.
DrugNov 17, 2021
Ezetimibe and Simvastatin Tablets, 10 mg/80mg, 500 tablet bottles recall — FDA D-0228-2022
Failed Excipient Specification; product manufactured using an excipient found to be OOS for conductivity
Class IIFDA: TerminatedGolden State Medical Supply Inc.
DrugNov 17, 2021
Acetaminophen Oral Suspension, 160 mg/5 mL recall — FDA D-0094-2022
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Class IIFDA: TerminatedPrecision Dose Inc.
DrugNov 17, 2021
Acetaminophen Oral Suspension, 325 mg/10.15 mL recall — FDA D-0095-2022
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Class IIFDA: TerminatedPrecision Dose Inc.
DrugNov 17, 2021
Ezetimibe and Simvastatin Tablets, 10 mg/40mg, a) 90 Tablets, b) 500 tablets recall — FDA D-0227-2022
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin…
Class IIFDA: TerminatedGolden State Medical Supply Inc.
VehicleNov 17, 2021
Camry vacuum recall — NHTSA campaign 21V890000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2018-2019 Camry vehicles. The vane cap inside the vacuum pump may break, causing the pump to fail, which could result…
vacuumToyota Motor Engineering & Manufacturing
VehicleNov 12, 2021
XC40 BEV engine recall — NHTSA campaign 21V881000
Volvo Car USA, LLC (Volvo) is recalling certain 2021 XC40 BEV vehicles. A bolt that secures the cross-member bracket for the electrical motor in the engine compartment may be loose or…
engineVolvo Car USA, LLC
VehicleNov 12, 2021
Mazda North American Operations fuel pump recall — NHTSA campaign 21V875000
Mazda North American Operations (Mazda) is recalling certain 2018 Mazda3, Mazda6, 2019 CX-3, 2018-2019 MX-5, CX-5, CX-9, and 2019-2020 Mazda2 vehicles. The impeller inside the low-pressure…
fuel pumpMazda North American Operations
VehicleNov 12, 2021
Chrysler fuel pump recall — NHTSA campaign 21V880000
Chrysler (FCA US, LLC) is recalling certain 2019-2020 Ram 2500, 3500 pickup trucks, and Ram 3500, 4500, and 5500 cab chassis vehicles equipped with Cummins 6.7L Turbo Diesel engines. The…
fuel pumpChrysler (FCA US, LLC)
Medical DeviceNov 10, 2021
Medtronic Neuromodulation Clinician Programmer Application (CPA) model A610 Clinician recall — FDA Z-0201-2022
A software anomaly may occur with the clinician programmer application.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceNov 10, 2021
FujiFilm Healthcare Americas Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 recall — FDA Z-0192-2022
When the ultrasound system is used in combination with a Fujifilm (formally Hitachi) transducer, there is an error in the calculation formula of Effective Regurgitant Orifice Area (EROA)…
Class IIFDA: OngoingFujiFilm Healthcare Americas Corporation
Medical DeviceNov 10, 2021
Cook Flexor Check-Flo Introducer, Introducer Set, RPN KCFW-6.0-35-45-RB, GPN G09908 The recall — FDA Z-0185-2022
Affected lots may be manufactured incorrectly with the radiopaque marker band located just below the Check-Flo proximal fitting instead of the distal tip. The issue may not be identified…
Class IIFDA: TerminatedCook Inc.
Medical DeviceNov 10, 2021
3M Company - Health Care Business 3M Red Dot Electrodes, Radiolucent Monitoring Electrode recall — FDA Z-0188-2022
Potential for breakage of the ECG electrode carbon stud from the eyelet.
Class IIFDA: Terminated3M Company - Health Care Business
Medical DeviceNov 10, 2021
FujiFilm Healthcare Americas Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 recall — FDA Z-0189-2022
Diagnostic ultrasound system with the specified software version and used in conjunction with a Fujifilm (formally Hitachi) transducer does not display the measurement results correctly…
Class IIFDA: OngoingFujiFilm Healthcare Americas Corporation
Medical DeviceNov 10, 2021
Siemens Medical Solutions USA Artis zeego, Fluoroscopic X-Ray System Models recall — FDA Z-0200-2022
Software error, the software can produce an incorrect interpretation of the table rotation if the table has been rotated by more than 4degrees in either direction. This can cause the 3D…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceNov 10, 2021
Bayer Medical Care The MEDRAD Twist & Go Disposable Syringe 150 mL with Quick Fill Tube is a recall — FDA Z-0199-2022
Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700 SYR) labeled as Twist & Go Syringes (TAG 150 SYR)
Class IIFDA: TerminatedBayer Medical Care, Inc.
Medical DeviceNov 10, 2021
Implant Direct Sybron Manufacturing ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x recall — FDA Z-0197-2022
Packaged dental implant contains a different size then the size declared on the labeling.
Class IIFDA: OngoingImplant Direct Sybron Manufacturing LLC
Medical DeviceNov 10, 2021
Siemens Healthcare Diagnostics Aptio Automation Interface Module to ADVIA Centaur XP/XPT recall — FDA Z-0193-2022
The Aptio Automation Firmware for the ADVIA Centaur XP/XPT Interface Module may lead, in some cases, to an incorrect association of test results to sample ID. Incorrect association of test…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceNov 10, 2021
Siemens Healthcare Diagnostics Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # recall — FDA Z-0195-2022
Data provided in the Emergency Use Authorization (EUA) submission was insufficient to determine that the assays were adequately validated for the intended use.
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceNov 10, 2021
FujiFilm Healthcare Americas Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 recall — FDA Z-0191-2022
Diagnostic ultrasound system with the specified software version and used in conjunction with a Fujifilm (formally Hitachi) transducer does not display the measurement results correctly…
Class IIFDA: OngoingFujiFilm Healthcare Americas Corporation
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
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