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 4316143180 of 46,762 recalls

DrugMay 13, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) Recalled by...

The Issue: Failed Impurity/Degradation Specifications; out of specification value for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 13, 2013· Life Technologies Corporation

Recalled Item: HSV 2 Primers Recalled by Life Technologies Corporation Due to Firm received...

The Issue: Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens issued a customer safety notice about the overlay of system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems...

The Issue: It has been confirmed from in-house testing that Direct Bilirubin (DBIL),...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Endologix Inc

Recalled Item: Brand Name: AFX" Introducer System Recalled by Endologix Inc Due to...

The Issue: Endologix, Inc. initiated this voluntary recall of certain lots of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2013· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister...

The Issue: Ethicon Endo-Surgery is initiating a voluntary worldwide recall for ECHELON...

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

Class II — Potential Health HazardOngoing
DrugMay 10, 2013· Apotex Corp.

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Corp. Due to...

The Issue: Crystallization: Potential to exhibit precipitation/crystallization in IV...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 10, 2013· ErgoSafe Product LLC dba Prism Medical Services

Recalled Item: 400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 Recalled by...

The Issue: MedCare Products has determined that a number of their Floor Lifts...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo(R) Lab Data Manager - Version VA11B and VA12A Systems Recalled by...

The Issue: Under certain conditions the system may not perform as intended, causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Rauland-Borg Corp

Recalled Item: Responder 5 is a nurse call communication system that connects Recalled by...

The Issue: A counterfeited electronic component was identified in the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· SpineFrontier, Inc.

Recalled Item: Invue Split Driver Recalled by SpineFrontier, Inc. Due to Device design.

The Issue: Device design.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: IMMULITE Systems Third Generation TSH ( - 100T Recalled by Siemens...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra ReadyPack (( - 100 Tests Recalled by...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension EXL LOCI Module TSHL Flex Reagent Cartridge (). Recalled by...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension Vista System TSH Flex Reagent Cartridge (). Intended Recalled by...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension TSH Flex Reagent Cartridge (). Intended to quantitatively Recalled...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: IMMULITE Systems Rapid TSH ( - 100T Recalled by Siemens Healthcare...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510449 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510636 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510180 Disposable Single Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing