Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,353 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,353 in last 12 months

Showing 2338123400 of 27,254 recalls

Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...

The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Biomet, Inc.

Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...

The Issue: Surface finish is different than specified. The implant has 30 grit blast on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Chemistry Controls Level I and II LEVl: Amber Recalled by...

The Issue: The original mean assigned to the control too high, upon reassignment with...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan -Neg Breakpoint Combo Panel Type 34 Recalled by Beckman Coulter,...

The Issue: Siemens Healthcare Diagnostics has received complaints regarding panel...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· Beckman Coulter Inc.

Recalled Item: Ultrasonic Transducer Kits For use with the Access Family of Recalled by...

The Issue: Beckman Coulter is initiating a field action because some Ultrasonic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· CooperSurgical, Inc.

Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...

The Issue: Sterility of the device may be compromised due to unsealed pouch

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Units may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing