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 · 6 months ago
Owen Biosciences Inc. FHF Farmhouse Fresh, Midnight Clearing, Night Lotion recall: Chemical contamination: Presence of benzene
Chemical contamination: Presence of benzene
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Class II · 6 months ago
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. MGC Health recall: This recall is being initiated following FDA's recommendation based
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the…
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Class II · 6 months ago
Sun Pharmaceutical Industries Inc Fluocinonide, USP, 0.05% Cream, 30g tube recall: Failed Viscosity Specifications: Out of Specification results
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
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NHTSA safety recall · 6 months ago
Hyundai recall: The B-pillar impact sensors may have been misassembled
The B-pillar impact sensors may have been misassembled, which can delay air bag deployment.
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Elevated risk · 7 months ago
Breeder’s Edge, Shelter’s Choice Canine milk replacer recall: Variable levels of Vitamin D
Variable levels of Vitamin D
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Class I · 7 months ago
Aligned Medical Angio Pack Angio Packs recall: Risk of the syringe rotating adapter unwinding during use
Risk of the syringe rotating adapter unwinding during use, which may result in a loose connection and/or full disconnection between the syringes and…
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Highest risk · 7 months ago
ZMC Group LED Finger Beam Lights recall: Risk of Serious Injury or Death from Battery Ingestion
Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
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Highest risk · 7 months ago
Macy's Arch Studio Tea Kettles recall: Risk of Serious Injury from Burn Hazard
Risk of Serious Injury from Burn Hazard
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Highest risk · 7 months ago
JC Sales Lil' Buddies Pet Laser Toys recall: Risk of Serious Injury or Death from Battery Ingestion Hazard
Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
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Highest risk · 7 months ago
Generac Power Systems Portable Generators recall: Risk of Serious Injury or Death from Burn and Fire Hazards
Risk of Serious Injury or Death from Burn and Fire Hazards
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Highest risk · 7 months ago
Fisher & Paykel Gas Ranges recall: The ovens in the ranges can experience a delayed ignition
The ovens in the ranges can experience a delayed ignition, causing gas to accumulate and the oven door to open from combustion, posing a burn hazard…
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Class II · 7 months ago
Spacelabs Healthcare, Inc. Multi-parameter Command Module, Model 91496 recall: Multi-parameter command module has a circuit board issue and when in Auto
Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing NAMIC Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline Industries, LP Namic Angiographic Syringe, labeled as follows: 1 recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class I · 7 months ago
Medline medical convenience kits, containing Namic Angiographic recall: Medline Industries, LP has identified through post-market surveillance
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…
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Class II · 7 months ago
Tornier HRS Max parts: 1. Tornier HRS Max Tuberosity Body Lat Coat recall: Affected products were incorrectly labeled as Tornier HRS Max products
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are…
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Class II · 7 months ago
Molded Products Inc See Luer Cap Set, MPC-130, set, administration, intravascular recall: Molded Products, Inc. is voluntarily conducting a medical device recall
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the…