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. 1,856 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,856 in last 12 months

Showing 3608136100 of 52,482 recalls

Medical DeviceMarch 25, 2016· Monteris Medical Corp

Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...

The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2016· Hansen Medical Inc

Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...

The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...

The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2016· Lupin Limited

Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2016· AbbVie Inc.

Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class III — Low RiskOngoing
Refund
FoodMarch 24, 2016· Nestle Infant Nutrition

Recalled Item: GERBER Organic 2ND FOODS Pears Recalled by Nestle Infant Nutrition Due to...

The Issue: Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 24, 2016· Nestle Infant Nutrition

Recalled Item: GERBER Organic 2ND FOODS¿ Carrots Recalled by Nestle Infant Nutrition Due to...

The Issue: Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2016· Teleflex Medical

Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...

The Issue: Incorrect expiration date was printed on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...

The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...

The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...

The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer complaint for the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: Chlorhexidine gluconate Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: PerioRx (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: ORIS (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· TMIG Inc

Recalled Item: Renovo Patch (Capsaicin Recalled by TMIG Inc Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Failed pH...

The Issue: Failed pH Specifications: Confirmed high out of specification (OOS) results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 23, 2016· Acumedia Manufacturers, Inc.

Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...

The Issue: Incorrect expiration date was listed on the label. Correct expiration date...

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

Class III — Low RiskOngoing