FoodDec 8, 2021
Alsum Farms & Produce 2 lbs recall — FDA F-0225-2022
Onions are being recalled by Keeler Family Farms due to potential Salmonella contamination.
Class IFDA: TerminatedAlsum Farms & Produce, Inc.
Latest records
Latest recalls — page 793
The newest recall records with useful source details are listed here.
FoodDec 8, 2021
Flowers Foods Tastykake Butterscotch Krimpets 24oz recall — FDA F-0236-2022
The firm was notified by an ingredient supplier of the potential small metal fragments in one of the ingredients.
Class IIFDA: TerminatedFlowers Foods (Corporate Offices)
FoodDec 8, 2021
Alsum Farms & Produce Whole Red onions packaged in 2lb recall — FDA F-0227-2022
Onions are being recalled by Keeler Family Farms due to potential Salmonella contamination.
Class IFDA: TerminatedAlsum Farms & Produce, Inc.
DrugDec 8, 2021
Lupin Pharmaceuticals Tydemy recall — FDA D-0264-2022
Subpotent Drug
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugDec 8, 2021
Sandoz Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic recall — FDA D-0286-2022
Temperature Abuse; temperature excursion during shipping
Class IFDA: CompletedSandoz Inc.
VehicleDec 8, 2021
Volkswagen Group of body control module/bcm recall — NHTSA campaign 21V947000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021-2022 Q5 Sportback, SQ5 Sportback, 2018-2022 Q5, and SQ5 vehicles. A liquid spill in the rear seat, or water ingress from…
body control module/bcmVolkswagen Group of America, Inc.
VehicleDec 2, 2021
Honda driveshaft recall — NHTSA campaign 21V939000
Honda (American Honda Motor Co.) is recalling certain 2021 Acura RDX and 2022 CR-V Hybrid vehicles. A component in the right or left front driveshaft may have been improperly heat-treated,…
driveshaftHonda (American Honda Motor Co.)
VehicleDec 2, 2021
Tucson electrical system software recall — NHTSA campaign 21V938000
Hyundai Motor America (Hyundai) is recalling certain 2022 Tucson vehicles. The software installed in the Integrated Central Control Unit (ICU) may be incompatible with the vehicle, which…
electrical system softwareHyundai Motor America
Medical DeviceDec 1, 2021
Siemens Medical Solutions USA Artis zee multi-purpose with software VD12-angiography systems recall — FDA Z-0298-2022
If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceDec 1, 2021
Medtronic Vascular Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT recall — FDA Z-0292-2022
Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube.
Class IIFDA: OngoingMedtronic Vascular, Inc.
Medical DeviceDec 1, 2021
Becton Dickinson Infusion Therapy Systems BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 recall — FDA Z-0306-2022
There is a breach in the product packaging that renders the product non-sterile.
Class IIFDA: OngoingBecton Dickinson Infusion Therapy Systems Inc.
Medical DeviceDec 1, 2021
Siemens Medical Solutions USA Artis Q.zen floor with software VD12-angiography systems recall — FDA Z-0303-2022
If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceDec 1, 2021
Philips Healthcare ProxiDiagnost N90 is multi-functional general R/F systems recall — FDA Z-0240-2022
The Aleva monitor requires certain labels to be applied, some of which are required by FDA Electronic Product Radiation Control performance standards. This includes the Radiation Warning…
Class IIFDA: OngoingPhilips Healthcare
Medical DeviceDec 1, 2021
GE Healthcare Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex recall — FDA Z-0242-2022
The accumulated dose is incorrectly displayed in certain situations. Thisoccurs during an interventional exam using the SmartStep option if the table height is adjusted after the exam…
Class IIFDA: OngoingGE Healthcare, LLC
Medical DeviceDec 1, 2021
Siemens Medical Solutions USA SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 recall — FDA Z-0289-2022
software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceDec 1, 2021
Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) recall — FDA Z-0238-2022
3D-RA is a reconstruction software product that can be used with the Philips Azurin system. This product extends the functionality of compatible X-ray equipment with the capability of 3D…
Class IIFDA: OngoingPhilips Healthcare
Medical DeviceDec 1, 2021
Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger Kit used by the recall — FDA Z-0293-2022
The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger Kits) become unresponsive if the charging steps, indicated in the Recharger Patient User Guide, are not followed.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceDec 1, 2021
Siemens Medical Solutions USA SOMATOM Drive with software syngo.CT VB20 Model #10431700 recall — FDA Z-0287-2022
software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceDec 1, 2021
Philips Healthcare DigitalDiagnost C90 recall — FDA Z-0239-2022
The Aleva monitor requires certain labels to be applied, some of which are required by FDA Electronic Product Radiation Control performance standards. This includes the Radiation Warning…
Class IIFDA: OngoingPhilips Healthcare
Medical DeviceDec 1, 2021
Siemens Medical Solutions USA Artis Q ceiling with software VD12-angiography systems recall — FDA Z-0301-2022
If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceDec 1, 2021
Philips Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - CT Vision ACQSIM recall — FDA Z-0277-2022
Significant wear of the Monitor Bracket Assembly shaft may go unrecognized could lead to the Monitor Bracket Assembly detaching from the Suspension Arm, and resulting in injury to patient,…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceDec 1, 2021
Siemens Medical Solutions USA SOMATOM Confidence with software syngo.CT VB20 Model #10590100 recall — FDA Z-0288-2022
software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in the delay in…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceDec 1, 2021
Abbott Laboratories ARCHITECT c4000 REF 02P24-01/2P24, 1P86, 1R24, and 1R25 recall — FDA Z-0272-2022
Twelve software-related issues affecting software version 9.41 and earlier were identified. The issues include bypassing error codes, incorrect calibration, loss of module communication…
Class IIFDA: OngoingAbbott Laboratories
Medical DeviceDec 1, 2021
Philips Healthcare CombiDiagnost R90 is multi-functional general R/F systems recall — FDA Z-0241-2022
The Aleva monitor requires certain labels to be applied, some of which are required by FDA Electronic Product Radiation Control performance standards. This includes the Radiation Warning…
Class IIFDA: OngoingPhilips Healthcare
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