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. 2,489 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,489 in last 12 months

Showing 2404124060 of 29,186 recalls

Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Thoracentesis & Paracentesis Procedure Tray Recalled by Pfm Medical Inc Due...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT 600 ml Drainage Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Microgenics Corporation

Recalled Item: MAS CardioImmune XL Cardiac Marker Control Recalled by Microgenics...

The Issue: MAS CardioImmune XL, level 1 (lot CXL16011), is showing vial-to-vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: 6F x 60 cm Dual Lumen CT PICC Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Pleural Drainage System Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2014· Biosense Webster, Inc.

Recalled Item: ThermoCool SmartTouch Navigation Catheters Recalled by Biosense Webster,...

The Issue: The recall was initiated because Biosense Webster is providing additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Rt Stand Off TI...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Rapid Neg Urine Combo Panel Type 1 Recalled by Siemens Healthcare...

The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Rt Standard Ti Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 55mm Rt Standard Ti Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Lft Stand Off Ti...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Rt Narrow Ti Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Lft Stand Off Ti...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 45mm Rt Standard TI Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Lft Narrow Ti Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Biomet Microfixation, LLC

Recalled Item: Total Temporomandibular Joint Replacement System- 50mm Rt Narrow Ti Mand...

The Issue: Laser etching on the parts is wider and deeper than the conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Ethicon, Inc.

Recalled Item: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet...

The Issue: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black...

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

Class II — Potential Health HazardOngoing