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. 2,518 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,518 in last 12 months

Showing 2004120060 of 29,186 recalls

Medical DeviceAugust 26, 2016· Philips Electronics North America Corporation

Recalled Item: HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A Recalled by...

The Issue: The handle can separate from the MRx housing due to breakage of mounts on...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS 1-Piece IOL Recalled by Abbott Medical Optics Inc. (AMO) Due to...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Multifocal 1-Piece Intraocular Lens Recalled by Abbott Medical Optics...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS 1-Piece IOL with the TECNIS iTec Preloaded Delivery System Recalled...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS OptiBlue 1-Piece IOL with the TECNIS iTec Preloaded Delivery System...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Teleflex Medical

Recalled Item: Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised...

The Issue: The connector may disconnect from the tracheostomy tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Symfony Extended Range of Vision IOL Recalled by Abbott Medical...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· CooperSurgical, Inc.

Recalled Item: Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation)...

The Issue: Products contain international package insert and not the correct USA...

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

Class III — Low RiskOngoing
Medical DeviceAugust 25, 2016· Sorin Group USA, Inc.

Recalled Item: St¿ckert S5 System Recalled by Sorin Group USA, Inc. Due to Sorin/LivaNova...

The Issue: Sorin/LivaNova is initiating a field correction on the S5 Heart-lung machine...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista IRON Flex reagent cartridges Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of deferoxamine interference...

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

Class III — Low RiskOngoing
Medical DeviceAugust 25, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Telemetry Receiver (XTR) Recalled by Spacelabs...

The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension IRON Flex reagent cartridges Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of deferoxamine interference...

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

Class III — Low RiskOngoing
Medical DeviceAugust 25, 2016· CooperSurgical, Inc.

Recalled Item: Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation)...

The Issue: Products contain international package insert and not the correct USA...

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

Class III — Low RiskOngoing
Medical DeviceAugust 24, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM) Recalled by Siemens...

The Issue: Siemens received multiple customer complaints indicating an increase in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Baxter Corporation Englewood

Recalled Item: 0.2 Micron Filter Recalled by Baxter Corporation Englewood Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for all...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...

The Issue: Siemens received multiple customer complaints indicating an increase in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Teleflex Medical

Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...

The Issue: Misbranded: Incorrect etching on the device.

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

Class II — Potential Health HazardOngoing