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. 1,877 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,877 in last 12 months

Showing 3246132480 of 52,482 recalls

Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Nidek Inc

Recalled Item: Final Fit Software Version 1.11 and 1.12 Recalled by Nidek Inc Due to During...

The Issue: During treatment planning, the procedure was programmed with an unintended...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Check-Flo Introducer Hausdorf-Lock Atrial Recalled by Cook Inc. Due to...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic Recalled by...

The Issue: Certain lots of Sex Hormone Binding Globulin (SHBG) do not meet the thirty...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
DrugJanuary 30, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled by Mylan...

The Issue: Chemical Contamination: out of specification results for impurities were...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Tarina Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled...

The Issue: Chemical Contamination: out of specification results for impurities were...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2017· Actavis Inc

Recalled Item: Glipizide extended-release tablets Recalled by Actavis Inc Due to Failed...

The Issue: Failed Dissolution Specifications. Above out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2017· Bwi Inc

Recalled Item: Burts British Hand Cooked Potato Chips Sea Salt & Malted Recalled by Bwi Inc...

The Issue: Product is labeled as gluten free; however was labeled as containing an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2017· Tearscience, Inc

Recalled Item: LipiFlow Thermal Pulsation System/LipiFlow Recalled by Tearscience, Inc Due...

The Issue: Labeling: The labeled storage temperature is not consistent with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2017· Beckman Coulter Inc.

Recalled Item: iChemVELOCITY Urine Chemistry System Recalled by Beckman Coulter Inc. Due to...

The Issue: The probe misalignment or bending has the potential to lead to delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2017· Phadia US Inc

Recalled Item: EliA Sample Diluent Recalled by Phadia US Inc Due to Erroneous EliA test...

The Issue: Erroneous EliA test results related to problems with liquid level detection...

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

Class II — Potential Health HazardOngoing