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. 1,938 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,938 in last 12 months

Showing 2418124200 of 52,482 recalls

Medical DeviceJanuary 31, 2019· RHONDIUM LIMITED

Recalled Item: Rhondium OVC3 One Visit Crown Recalled by RHONDIUM LIMITED Due to Mislabeling

The Issue: The product was mislabeled with an incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2019· Medline Industries Inc

Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...

The Issue: Potential for the Semi-Rigid canister lid to fragment during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2019· Microbiologics Inc

Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...

The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...

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

Class II — Potential Health HazardOngoing
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Diltiazem HCl CD capsules Recalled by Valeant Pharmaceuticals North America...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 30, 2019· U&I CORP.

Recalled Item: Velofix SA cervical cage Recalled by U&I CORP. Due to The vertical...

The Issue: The vertical dimensions of screw-hole position in some standalone cages...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2019· Matrix Surgical Holdings, LLC

Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...

The Issue: Product mislabeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2019· Matrix Surgical Holdings, LLC

Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...

The Issue: Product mislabeling.

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2019· US Compounding Inc

Recalled Item: Ephedrine Sulfate Recalled by US Compounding Inc Due to Lack of assurance of...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2019· COLLINS AEROSPACE

Recalled Item: TASE 400 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...

The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2019· COLLINS AEROSPACE

Recalled Item: TASE 500 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...

The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Lupin Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications: OOS results observed in any...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX2 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX3 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX3 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX2 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Spacelabs Healthcare, Inc.

Recalled Item: Spacelabs Healthcare Smart Disclosure System Recalled by Spacelabs...

The Issue: Several reports were received that patient records were printed with the...

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

Class II — Potential Health HazardOngoing