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. 2,478 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,478 in last 12 months

Showing 2556125580 of 29,186 recalls

Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Spacelabs Healthcare, Llc

Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...

The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Steris Corporation

Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...

The Issue: STERIS has identified that the outer shipping package for one lot (Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...

The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Zimmer, Inc.

Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...

The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...

The Issue: Three problems were reported to the firm: When positioning for a relative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 9-12 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Urine Control L/H. The ABX PENTRA Urine Control Recalled by...

The Issue: HORIBA Medical is informing all ABX PENTRA Urine Control L/H customers...

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

Class III — Low RiskOngoing
Medical DeviceDecember 18, 2013· Merit Medical Systems, Inc.

Recalled Item: Radial Assist RAD BOARD Recalled by Merit Medical Systems, Inc. Due to Merit...

The Issue: Merit Medical Systems, Inc. is voluntarily recalling one lot (B507171) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Ranir Corporation

Recalled Item: UP & UP kids' power toothbrush Recalled by Ranir Corporation Due to Ranir,...

The Issue: Ranir, LLC is recalling all lots of UP & UP brand Kid's Power Toothbrush and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Ranir Corporation

Recalled Item: TopCare Clifford THE BIG RED DOG power toothbrush for kids! Recalled by...

The Issue: Ranir, LLC is recalling all lots of Up & Up brand Kid's Power Toothbrush and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Stryker Spine

Recalled Item: Specialty Straight Static Inserter Assembly Product Usage: This instrument...

The Issue: Stryker has received complaints from customers relating to fracture along...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 6-pack SMN Recalled by...

The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...

The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2013· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: Possible break in the connector of the Force Sensor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs: 2MM Carbide Fluted Ball Recalled by The...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Carbide Cutting Burrs & Drums: 2MM Carbide Fluted Ball Recalled by...

The Issue: Some carbide cutting burr fractured during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine...

The Issue: Bicarbonate Jug Adapter distributed prior to 510(k) approval

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

Class II — Potential Health HazardOngoing