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. 959 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
959 in last 12 months

Showing 44661–44680 of 52,120 recalls

Medical DeviceFebruary 7, 2014· Leica Biosystems Imaging, Inc.

Recalled Item: HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Recalled by...

The Issue: In an abundance of caution, Aperio (now known as Lecia Biosystems) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· Baxter Healthcare Corp.

Recalled Item: SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product...

The Issue: Baxter Healthcare Corporation has issued an Urgent Device Correction for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis Systems Product usage: Artis zee is a family Recalled by Siemens...

The Issue: Certain units of the AXIOM Artis Systems are using a flat detector cooling...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee Angiographic x-ray systems. Recalled by Siemens Medical Solutions...

The Issue: An inappropriate cable connection was assembled for certain Artis zee...

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

Class II — Potential Health HazardOngoing
DrugFebruary 7, 2014· Actavis

Recalled Item: Gelnique (oxybutynin chloride) Gel 10% Recalled by Actavis Due to Subpotent...

The Issue: Subpotent Drug: Drug potency was compromised during shipment.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 6, 2014· Mars Food US

Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...

The Issue: Reports of mild flushing reaction after consumption of product led to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...

The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2014· Medtronic Vascular

Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...

The Issue: Incorrect master label.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 5, 2014· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...

The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Synthes, Inc.

Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...

The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Fisher Scientific Co

Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...

The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...

The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...

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

Class II — Potential Health HazardOngoing