Recalls affecting Wisconsin
Notices that name Wisconsin in their distribution area, plus every nationwide recall — nationwide recalls reach Wisconsin too.
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
Raz-AT Mobile Shower Commode Chair recall: Due to a modification by a vendor and may be reinstalled without properly
Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in…
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model SL Connection Component incl. PE-Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 8 months ago
International Life Sciences Artelon FlexBand Dynamic Matrix Ref: 31057 recall: Augmentation devices failed bacterial endotoxin testing
Augmentation devices failed bacterial endotoxin testing.
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Class II · 8 months ago
Beckman Coulter Mishima K.K. Chemistry Analyzer AU5800, REF: B96697, B96698 recall: A delay in results may occur. When clinical chemistry analyzer calibration
A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open…
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Class II · 8 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class III · 8 months ago
Penner Pacific Bathing Spa, Model Numbers 360020-1P recall: The device does not bear a unique device identifier
The device does not bear a unique device identifier.
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Class II · 8 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 8 months ago
Zydus Pharmaceuticals Inc Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle recall: Failed Tablet/Capsule specifications: Red dots inside capsule and melted
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
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Class II · 8 months ago
Palmetto Gourmet Foods Inc. Vegetarian Chicken Flavor Ramen Express recall: Product contains undeclared Yellow #5
Product contains undeclared Yellow #5
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Class II · 8 months ago
Palmetto Gourmet Foods Inc. Vegetarian Chicken Flavor Ramen Express recall: Product contains undeclared Yellow #5
Product contains undeclared Yellow #5
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NHTSA safety recall · 8 months ago
Ford F-59 and F-53 commercial stripped chassis recall: The exterior brake lights may remain illuminated when the driver
The exterior brake lights may remain illuminated when the driver is not applying the brakes. As such, these vehicles fail to comply with the…
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NHTSA safety recall · 8 months ago
Ford Explorer and Lincoln Aviator recall: The seat belt anchor bolts at the second-row outer seating positions
The seat belt anchor bolts at the second-row outer seating positions may be improperly secured.
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NHTSA safety recall · 8 months ago
Chrysler Jeep Wagoneer S recall: The liftgate hinge cover may not be properly clipped into position
The liftgate hinge cover may not be properly clipped into position and may detach from the vehicle.
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Highest risk · 8 months ago
Stoney Games Kluster Magnet Chess Games recall: Risk of Serious Injury or Death from Magnet Ingestion
Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
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Highest risk · 8 months ago
ProRider Bicycle Helmets recall: Risk of Serious Injury or Death from Head Injury
Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
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Elevated risk · 8 months ago
Lfte USA Playground Swing Set Seats recall: Fall Hazard
Fall Hazard
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NHTSA safety recall · 8 months ago
Volvo Car EX30 and EX30CC recall: The seat belt warning system may not activate the audible warning chime
The seat belt warning system may not activate the audible warning chime as intended. As such, these vehicles fail to comply with the requirements of…
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NHTSA safety recall · 8 months ago
Volkswagen Jetta recall: The transmission ground wire may not have been properly connected during
The transmission ground wire may not have been properly connected during assembly, causing an open electrical circuit.
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class II · 8 months ago
Vascutek, Ltd. Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE recall: Gelatin sealed woven polyester prostheses devices
Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life…