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. 2,621 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,621 in last 12 months

Showing 1292112940 of 29,186 recalls

Medical DeviceOctober 29, 2019· Bio-Signal Group Corp.

Recalled Item: HydroDot brand: Wave Prep Single use cups Recalled by Bio-Signal Group Corp....

The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer Private Label Item Code: 3069 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of...

The Issue: Current software version of the Anti-HAV IgM APP-file (version 06.05-101)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Bard Peripheral Vascular Inc

Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...

The Issue: During the firm's review of May 2019 complaint data, a significant increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Conformis, Inc.

Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...

The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic...

The Issue: Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 14MM- Orthopedic...

The Issue: Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2019· Galil Medical, Inc.

Recalled Item: Visual-ICE Cryoablation System Recalled by Galil Medical, Inc. Due to...

The Issue: Visual-ICE utilizing the IceSeed 1.5 and IceRod 1.5 PLUS cryoablation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Applied Medical Resources Corp

Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...

The Issue: The firm has received reports of tip separation during usage of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...

The Issue: Sterile packaging incomplete seals may compromise sterility of the product

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

Class II — Potential Health HazardOngoing