Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 2704127060 of 27,655 recalls

Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP PN 98000XR Intended to be used as Recalled by Alere San...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal software Product Usage: Intellispace Portal is a...

The Issue: In the Multi-Modality Tumor Tracking application, when changing the contours...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage Cardiac Panel PN 97000HS Used for the quantitative Recalled by...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage Profiler SOB Panel PN 97300 Used for the Recalled by Alere San...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Triage D-dimer PN 98100 Used as an aid in the Recalled by Alere San Diego,...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Synthes USA HQ, Inc.

Recalled Item: 4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 .019.038S...

The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage CardioProfiler Panel PN 97100CP Used for the quantitative...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Synthes USA HQ, Inc.

Recalled Item: 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 .019.028S...

The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: TetraCXP Software System Recalled by Beckman Coulter Inc. Due to The recall...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Natus Medical Incorporated

Recalled Item: Olympic Cool-Cap System is intended to provide treatment for neonatal...

The Issue: Olympic Cool-Cap Cooling Module's power supply failed during treatment. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to software...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Software For use in the in-vitro quantitative...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Stryker Endoscopy

Recalled Item: Formula Shaver Handpiece (with buttons) Recalled by Stryker Endoscopy Due to...

The Issue: Stryker Endoscopy determined that there may not have been adequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Software For use in the in-vitro quantitative...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Philips Healthcare Inc.

Recalled Item: Philips Multi Diagnost Eleva II with swivel cable Product Codes Recalled by...

The Issue: MultiDiagnost Eleva X--Ray system may have damage to System Cables from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing