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. 984 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
984 in last 12 months

Showing 42721–42740 of 52,482 recalls

Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
FoodOctober 20, 2014· Bailey Farms, Inc.

Recalled Item: Bailey Farms Recalled by Bailey Farms, Inc. Due to Potential Salmonella...

The Issue: Product was found to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 19, 2014· Biosense Webster, Inc.

Recalled Item: ThermoCool SmartTouch Navigation Catheters Recalled by Biosense Webster,...

The Issue: The recall was initiated because Biosense Webster is providing additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...

The Issue: Cardiohelp- i System may have a software issue that can potentially result...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Rapid Neg Urine Combo Panel Type 1 Recalled by Siemens Healthcare...

The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Rapid Neg BP Combo Panel Type 3 Recalled by Siemens Healthcare Diagnostics,...

The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2014· Ethicon, Inc.

Recalled Item: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet...

The Issue: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black...

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

Class II — Potential Health HazardOngoing
DrugOctober 17, 2014· Obagi Medical Products

Recalled Item: Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2014· Aurobindo Pharma USA Inc

Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Complaints of empty capsules received.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2014· Hospira Inc.

Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of particulate matter: A returned customer sample was evaluated and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 16, 2014· Pharmaceutical Associates Inc

Recalled Item: Cyproheptadine HCl Syrup (Cyproheptadine HCl Oral Solution Recalled by...

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
DrugOctober 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing