Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,693 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,693 in last 12 months

Showing 661680 of 52,120 recalls

Medical DeviceNovember 20, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Baby Allergy Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Pain Away Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Baby Soothe Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Boswellia Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Ear Drops Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Anti-virus Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Sinus Cap Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Organic Ginger Root Herbal Supplement Recalled by A New Life Herbs, LLC Due...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2025· A New Life Herbs, LLC

Recalled Item: Chaga Mushroom Herbal Supplement Recalled by A New Life Herbs, LLC Due to...

The Issue: Unapproved drug claims on product labeling and product misbranded due to no...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· DICOM Grid, Inc.

Recalled Item: Intelerad InteleShare software Recalled by DICOM Grid, Inc. Due to Software...

The Issue: Software intended to aid in diagnosing conditions, planning treatments,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 18, 2025· JR Simplot Company

Recalled Item: Simplot¿ Traditional Reduced Sodium Tater Gems¿ Recalled by JR Simplot...

The Issue: Plastic fragments. Pieces of semi-rigid plastic embedded in the recalled...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Nebivolol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Cross Contamination with Other Products

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 18, 2025· AGFA Healthcare Corp.

Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...

The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...

The Issue: When the Worstation of the BeneVision DMS has a specific hardware...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...

The Issue: A customer experienced that during assembly and load testing of the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sophysa

Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...

The Issue: Customer complaints of Pressio monitor rebooting.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing