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 3466134680 of 52,482 recalls

Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2016· Mylan Pharmaceuticals Inc.

Recalled Item: Alprazolam Extended-release Tablets Recalled by Mylan Pharmaceuticals Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2016· Teva North America

Recalled Item: Albuterol Sulfate Syrup Recalled by Teva North America Due to Presence of...

The Issue: Presence of Foreign Substance; presence of black particles describes...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
FoodJune 21, 2016· Kill Cliff

Recalled Item: KC (Kill Cliff) Strawberries & Cream Protein Bars Recalled by Kill Cliff Due...

The Issue: Product may contain mold. Recall started on 6/21/16

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2016· Karl Storz Endoscopy

Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...

The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2016· Medtronic Navigation

Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...

The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Integra LifeSciences Corp.

Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...

The Issue: Data from internal studies suggests there may be a potential that the...

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

Class II — Potential Health HazardOngoing
FoodJune 17, 2016· Annona Company, LLC

Recalled Item: Earnest Eats Chewy Granola Dark Chocolate Almond .2 Recalled by Annona...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 17, 2016· Fresh Express Incorpated

Recalled Item: Fresh Express Kit Caesar salad Recalled by Fresh Express Incorpated Due to...

The Issue: The condiment kits in some Caesar Salad bags contain undeclared allergens:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund