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. 2,576 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,576 in last 12 months

Showing 1652116540 of 29,186 recalls

Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Double-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: SnapLock" Catheter/Syringe Adapter Recalled by Arrow International Inc Due...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Cenorin, LLC

Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...

The Issue: There is a supplier quality issue with the terminal blocks which may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Box Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: T-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· MHC Medical Products LLC

Recalled Item: EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Recalled...

The Issue: The retail shelf cartons may be labeled with an incorrect lot number.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Non-Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: CC Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· MHC Medical Products LLC

Recalled Item: EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Recalled by...

The Issue: The retail shelf cartons may be labeled with an incorrect lot number.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: TN Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival Reduce Kit Plates Recalled by Orthofix, Inc Due to Firm is conducting...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing