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. 1,786 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
1,786 in last 12 months

Showing 4354143560 of 52,482 recalls

Medical DeviceJune 18, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF PET/CT16: 882470 Recalled by Philips Medical Systems (Cleveland)...

The Issue: When beginning a procedure to start the gantry and CT Host, a Close Estop...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2014· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen)...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Apri (desogestrel and ethinyl estradiol tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2014· Varian Medical Systems, Inc.

Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...

The Issue: Trend in reports of unexpected decrease in beam output in C-series High...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Syngo RT Therapist and Syngo RT Oncologist intended use Recalled by...

The Issue: Siemens became aware of a potential issue with the syngo RT Therapist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...

The Issue: Inadequate iodine and packaging related defects.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
DrugJune 16, 2014· Baxter Healthcare Corp.

Recalled Item: Brevibloc Premixed Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Complaints received of discolored solution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 16, 2014· Nidek Inc

Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...

The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2014· McKesson Technologies, Inc.

Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...

The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2014· Schnucks Markets Inc

Recalled Item: Schnucks Bakery 8" Devil's Food Cake Recalled by Schnucks Markets Inc Due to...

The Issue: The product contains pecan pieces as a top garnish and the product label...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2014· Vita Food Products, Inc.

Recalled Item: Vita Classic Premium Sliced Smoked Atlantic Nova Salmon Recalled by Vita...

The Issue: This voluntary recall is being initiated due to a positive Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 13, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...

The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing