Recalls affecting Minnesota
Notices that name Minnesota in their distribution area, plus every nationwide recall — nationwide recalls reach Minnesota too.
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Class II · 9 months ago
Merit Medical Systems, Inc. Allwell recall: Inflation device handle may detach from the syringe during procedure
Inflation device handle may detach from the syringe during procedure.
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Class II · 9 months ago
Brand Name: EDAN Product Name: Vital Signs Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Brand Name: EDAN Product Name: Fetal Monitor Model/ recall: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm…
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Class II · 9 months ago
Specialty Process Labs LLC Thyroid, USP recall: Subpotent Drug
Subpotent Drug
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Class II · 9 months ago
Graviti Pharmaceuticals Private Limited Furosemide Tablets, USP 40 mg, 1,000 Tablets recall: Presence of Foreign Substance
Presence of Foreign Substance
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Class II · 9 months ago
Zydus Pharmaceuticals Inc Icosapent Ethyl capsules, 1 gram, 120-count bottles recall: Subpotent Drug: Due to oxidation caused by leakage of the contents
Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules
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Class III · 9 months ago
Cipla USA, Inc. Diclofenac Sodium Topical Gel, 1% recall: Failed PH Specifications
Failed PH Specifications
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NHTSA safety recall · 9 months ago
Kia recall: Due to a software error, the instrument panel display may fail
Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle…
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NHTSA safety recall · 9 months ago
Hyundai recall: Due to a software error, the instrument panel display may fail
Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle…
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Class II · 9 months ago
Gerber Arrowroot biscuits recall: potential presence of soft plastic and/or paper pieces
potential presence of soft plastic and/or paper pieces
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NHTSA safety recall · 9 months ago
Toyota Tundra and Tundra Hybrid recall: The rearview camera image may not display when the vehicle is placed
The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of…
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NHTSA safety recall · 9 months ago
Hyundai Palisade recall: The side curtain air bags for third-row occupants may deploy improperly
The side curtain air bags for third-row occupants may deploy improperly in a crash. As such, these vehicles fail to comply with the requirements of…
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NHTSA safety recall · 9 months ago
General Chevrolet Blazer EV recall: The rear parking brake wiring harness may become damaged or corroded
The rear parking brake wiring harness may become damaged or corroded, resulting in unintended activation of the parking brake or loss of the parking…
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Elevated risk · 9 months ago
Thrasio Angry Orange Enzyme Stain Removers recall: Risk of Exposure to Bacteria
Risk of Exposure to Bacteria
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Elevated risk · 9 months ago
Academy Sports + Outdoors Magellan Odyssey Rocker Chairs recall: Injury and Fall Hazards
Injury and Fall Hazards
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NHTSA safety recall · 9 months ago
Volkswagen ID.4 recall: 4 vehicles. The high-voltage battery may overheat
4 vehicles. The high-voltage battery may overheat.
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NHTSA safety recall · 9 months ago
Nissan recall: The door strikers may have been improperly welded and break
The door strikers may have been improperly welded and break, allowing the door to open while moving. As such, these vehicles fail to comply with the…
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NHTSA safety recall · 9 months ago
Ford F-59 and F-53 recall: The exterior brake lights may illuminate unexpectedly or fail to illuminate
The exterior brake lights may illuminate unexpectedly or fail to illuminate when the brake pedal is activated, due to an incorrectly installed…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Robotic recall: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the…
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Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
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Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
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Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
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Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
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Class II · 9 months ago
C-Rad Positioning Ab Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/ recall: Due to issues with the system's stereotactic radiosurgery (SRS) treatment
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain…