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. 2,654 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,654 in last 12 months

Showing 72017220 of 52,120 recalls

Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Flo-Rester Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Coseal Premix Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Abiomed, Inc.

Recalled Item: Impella Connect Recalled by Abiomed, Inc. Due to The following features have...

The Issue: The following features have been disabled from the web-based portal because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table version Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Ambu Inc.

Recalled Item: Ambu aView 2 A Monitor Recalled by Ambu Inc. Due to Instructions for Use...

The Issue: Instructions for Use have been updated to add the following warning: Use...

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

Class II — Potential Health HazardOngoing
FoodDecember 4, 2023· Lunds Mitchell Rd LLC

Recalled Item: Lunds & Byerlys grilled chicken caesar salad Recalled by Lunds Mitchell Rd...

The Issue: Korean Shrimp Salad may be mislabeled as Grilled Chicken Caesar Salad:...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund