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. 1,776 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,776 in last 12 months

Showing 5190151920 of 52,482 recalls

Medical DeviceMay 1, 2012· Nidek Medical Products Inc

Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...

The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.

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

Class I — Serious Health HazardOngoing
FoodMay 1, 2012· Smart Juice LLC

Recalled Item: Organic 100% Pomegranate Juice packed in glass bottles Smart Juice Recalled...

The Issue: Pomegranate juice contains levels of lead above allowable limits.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2012· Apotex Inc.

Recalled Item: Dorzolamide HCI/Timolol Maleate Ophthalmic Solution 22.3mg/6.8mg per mL...

The Issue: Presence of Particulate Matter: Lots identified in this recall notification...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 30, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah Recalled by...

The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Zimmer Inc.

Recalled Item: Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral Recalled...

The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Uroskop Access. Fluoroscopic Recalled by Siemens Medical Solutions...

The Issue: Siemens has discovered a possible hazard to patients or hospital personnel...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray...

The Issue: During regular product monitoring, firm became aware of a potential issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Rejuvenate Modular Stems Stryker Ireland Carrigtwohill Industrial Estate...

The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2012· Zimmer Inc.

Recalled Item: Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor...

The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: Newport Portable Package Recalled by Accutron Inc Due to Accutron is...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: Ultra PC% Cabinet Mount Package G Recalled by Accutron Inc Due to Accutron...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: CM Flowmeter Pkg H Recalled by Accutron Inc Due to Accutron is recalling the...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2012· Accutron Inc

Recalled Item: Flow Meter Recalled by Accutron Inc Due to Accutron is recalling the...

The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2012· Kimberly-Clark Corporation

Recalled Item: Kimberly Clark Patient Warming System - Model 1000 Control Unit. Recalled by...

The Issue: A defect of the "fuse holder" can lead to a Control Unit failure that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2012· Respironics, Inc.

Recalled Item: Respironics Trilogy 100 Recalled by Respironics, Inc. Due to The specified...

The Issue: The specified Trilogy units are being recalled because of the potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2012· Motorola Inc

Recalled Item: Motorola Solutions PCS3000/CS3070 Laser Utility/Peripheral Laser Products...

The Issue: It was discovered the CS3000/CS3070 was manufactured using the laser power...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2012· Plasma Surgical Inc.

Recalled Item: PlasmaJet Open Surgery Handpiece (Part of the PlasmaJet Neutral Plasma...

The Issue: Potential failure in the glued seal between the stem and the tip of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2012· MicroAire Surgical Instruments, LLC

Recalled Item: Lipofilter 3000 Recalled by MicroAire Surgical Instruments, LLC Due to...

The Issue: Medical device was not manufactured under Good Manufacturing Procedures and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2012· Ormco/Sybronendo

Recalled Item: The brand name of the device is Damon 3MX Bicuspid Bracket Recalled by...

The Issue: The firm initiated the recall as a result of a misidentification of the...

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

Class III — Low RiskOngoing
DrugApril 24, 2012· Luitpold Pharmaceuticals, Inc.

Recalled Item: Epinephrine Injection Recalled by Luitpold Pharmaceuticals, Inc. Due to...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund