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 4952149540 of 52,482 recalls

Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and...

The Issue: The firm has received numerous complaints of the cannulated screw driver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Exactech, Inc.

Recalled Item: Optetrak Logic Comprehensive Knee Prosthesis System Recalled by Exactech,...

The Issue: A dimensional mismatch was identified which can potentially allow for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Orthofix, Inc

Recalled Item: Firebird Spinal Fixation System Recalled by Orthofix, Inc Due to There is a...

The Issue: There is a possibility that the Set Screw (p/n 90-2923) sub-component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE Safety Blood Collection Set + Luer Adapter Recalled by Greiner...

The Issue: The VACUETTE Safety Blood Collection Set + Luer Adapter may display leaking...

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

Class II — Potential Health HazardOngoing
DrugJanuary 31, 2013· Gilead Sciences, Inc.

Recalled Item: Vistide (cidofovir) Injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: Particulate matter was found in some vials...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 31, 2013· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax (cefixime for oral suspension) USP Recalled by Lupin Pharmaceuticals...

The Issue: Discoloration; Product may not meet specifications for color description...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 31, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus...

The Issue: During the course of product monitoring, Siemens became aware of a tolerance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2013· Hitachi Medical Systems America Inc

Recalled Item: Echelon Recalled by Hitachi Medical Systems America Inc Due to Hitachi...

The Issue: Hitachi discovered a software error that can occur when simultaneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2013· Salyer Prn Biomedical

Recalled Item: Century Console Base Recalled by Salyer Prn Biomedical Due to Concerns that...

The Issue: Concerns that the addition of the UPS Battery Backup to the Century Console...

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

Class II — Potential Health HazardOngoing