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. 1,917 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,917 in last 12 months

Showing 2698127000 of 52,482 recalls

Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: ADVANSYS MLP/DLP Recalled by NewDeal SA Due to Use of the impacted product...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...

The Issue: The recalling firm has received a higher than expected number of complaints...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2018· Medline Industries Inc (Northpoint Services)

Recalled Item: READYFLUSH PROTECT with Dimethicone (3.2%) Recalled by Medline Industries...

The Issue: Microbial Contamination of a Non-Sterile Product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 21, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...

The Issue: The block used to connect the patient pallet to the couch may be assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Modular Primary Tibial Tray Implants Recalled by Zimmer Biomet, Inc....

The Issue: One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· OMNIlife science Inc.

Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...

The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...

The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Qiagen Sciences, Inc.

Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...

The Issue: Potential for control line not appearing on the test strip

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 18, 2018· BERLIN HEART GMBH

Recalled Item: EXCOR Pediatric Ventricular Assist Device Blood Pumps Recalled by BERLIN...

The Issue: There is a potential for a disruption in one or more of the triple layer...

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

Class I — Serious Health HazardOngoing
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Sully's Potato Salad Recalled by Morski Brands Inc. dba Dawn's Fresh Foods...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Terry's Potato Salad Recalled by Morski Brands Inc. dba Dawn's Fresh Foods...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Finest Traditions Deluxe Potato Salad Recalled by Morski Brands Inc. dba...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2018· Morski Brands Inc. dba Dawn's Fresh Foods

Recalled Item: Dawn's Foods Deluxe Potato Salad Mfg. No. 20114 Recalled by Morski Brands...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 17, 2018· Ziyad Brothers Importing, Inc.

Recalled Item: Ziyad Brand Tahini Recalled by Ziyad Brothers Importing, Inc. Due to...

The Issue: Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing