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 I · 6 months ago
Zapp’s, Dirty Potato chips recall: Potential Foodborne Illness - Salmonella
Potential Foodborne Illness - Salmonella
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Class I · 6 months ago
a2 a2 Platinum Premium Infant Formula 0-12 months USA label recall: Presence of cereulide toxin produced by some strains of the bacterium
Presence of cereulide toxin produced by some strains of the bacterium Bacillus cereus
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Class II · 6 months ago
Second Nature Keto Crunch Smart Mix recall: May contain undeclared Cashews, Pistachios, and Cherries
May contain undeclared Cashews, Pistachios, and Cherries
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NHTSA safety recall · 6 months ago
Mercedes-Benz CLA 350 4MATIC and CLA 250+ recall: The front passenger seat belt retractor may have been manufactured
The front passenger seat belt retractor may have been manufactured with a defect that prevents the deactivation of the child seat safety function…
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NHTSA safety recall · 6 months ago
Mercedes-Benz recall: The infotainment control unit may reset while the vehicle is in motion
The infotainment control unit may reset while the vehicle is in motion and cause the instrument panel display to go blank.
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Highest risk · 6 months ago
Thermos 8.2 Million Stainless King Food Jars and Bottles recall: Serious Impact Injury and Laceration Hazards
Serious Impact Injury and Laceration Hazards
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Highest risk · 6 months ago
Residential Elevators Elevator StrikeLock Hoistway Door Locking Device recall: Risk of Serious Injury or Death from Fall and Injury Hazards
Risk of Serious Injury or Death from Fall and Injury Hazards
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Highest risk · 6 months ago
CBC Group Stephan Baby Boo Bunnie and Friends Children's Toys recall: Risk of Serious Injury from Choking and Laceration Hazards
Risk of Serious Injury from Choking and Laceration Hazards
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Highest risk · 6 months ago
American Honda Motor Off-Road Motorcycles recall: Risk of Serious Injury or Death Due to Crash Hazard
Risk of Serious Injury or Death Due to Crash Hazard
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Public Health Alert · 6 months ago
FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Dairy Products That Have Been Recalled Due to Possible…
Product Contamination
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Class II · 6 months ago
Olympus Corporation of the Americas OER-ELITE Endoscope Reprocessor Connecting Tubes recall: Potential for the Version 2 reprocessor connecting tube lock levers may fail
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
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Class II · 6 months ago
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate recall: Unapproved design changes to the products outside of the 510(k) clearance
Unapproved design changes to the products outside of the 510(k) clearance.
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Class II · 6 months ago
Medline Kits: 1) Arthrogram Tray recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Medline Kits: 1) D AND C PACK recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Angiodynamics, Inc. Soft-Vu Angiographic Catheter, Headhunter , Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
XTANT Medical Holdings, Inc nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus recall: Products were incorrectly labeled with a 5-year shelf life. The approved
Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
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Class II · 6 months ago
Angiodynamics, Inc. Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
Angiodynamics, Inc. Soft-Vu Angiographic Catheter, Cobra , Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
Remel Europe Ltd. Oxoid Agglutinating Sera, Salmonella 9-0 R30957301 recall: Affected lots are not performing to IFU criteria showing cross reactions
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the…
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Class II · 6 months ago
Medline Kits: 1) Angio Cath Pack-Mary Immaculat recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Sequencing Agent SEQ0067, component of FoundationOne CDx recall: Possible increase in phasing, potentially resulting in false-positive BARD1
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants
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Class II · 6 months ago
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate recall: Unapproved design changes to the products outside of the 510(k) clearance
Unapproved design changes to the products outside of the 510(k) clearance.
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Class II · 6 months ago
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Windstone Medical Packaging, Inc. Custom Convenience Kits Pre Op Kit - NS recall: The product correction was initiated because B Braun is issuing a voluntary
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as…