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. 2,258 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,258 in last 12 months

Showing 4340143420 of 46,762 recalls

Medical DeviceApril 15, 2013· Medrad Inc

Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...

The Issue: The firm is recalling these power cables due to a latent design reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Hill-Rom, Inc.

Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...

The Issue: Complaints have been reported for brakes disengaging when the bed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...

The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...

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

Class I — Serious Health HazardOngoing
DrugApril 12, 2013· OPMX, LLC

Recalled Item: Pentrexcilina Jarabe NF (dextromethorphan HBr and guaifenesin) liquid...

The Issue: Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 12, 2013· OPMX, LLC

Recalled Item: Pentrexcilina (acetaminophen Recalled by OPMX, LLC Due to Labeling: Not...

The Issue: Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2013· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Paa Laboratories Inc

Recalled Item: Various types of Fetal Bovine Serum Bovine sourced Animal Sera Recalled by...

The Issue: Current product labeling band data sheets state that FBS Pharma Grade and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Covidien LLC

Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...

The Issue: On March 26, 2013 Covidien received a recall notice from one of their...

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

Class III — Low RiskOngoing
Medical DeviceApril 12, 2013· Becton Dickinson & Co.

Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...

The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Becton Dickinson & Co.

Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...

The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing