Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,557 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,557 in last 12 months

Showing 2022120240 of 28,744 recalls

Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color A1 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color A2 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color B1 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color A3.5 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color C2 60ml art. no. 681060. Product Usage: Recalled by...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: ONLINE TDM Vancomycin 100 tests Recalled by Roche Diagnostics Operations,...

The Issue: Roche Diagnostics Operations, Inc. has issued a voluntary recall for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...

The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN...

The Issue: Eight (8) issues were identified which may affect the results generated by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Exactech, Inc.

Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...

The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2016· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The surface inside of the femoral component, where cement is applied for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Physio-Control, Inc.

Recalled Item: LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External...

The Issue: LIFEPAK CR Plus Automated External Defibrillators (AED) or LIFEPAK EXPRESS...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access software. The firm name on the label is Merge Healthcare...

The Issue: Software displayed incorrect prior reports in the viewport area, only when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to The...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Recalled by Philips Medical Systems (Cleveland)...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Upgrade Model 882454 Recalled by Philips Medical Systems...

The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...

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

Class II — Potential Health HazardOngoing