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. 2,384 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,384 in last 12 months

Showing 1874118760 of 27,254 recalls

Medical DeviceAugust 18, 2016· Elekta, Inc.

Recalled Item: HexaPOD evo RT System Product Usage: The intended use of Recalled by Elekta,...

The Issue: Potentially unrecognized incorrect position of the treatment couch in 3D...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Used to make treatment plans for patients Recalled by...

The Issue: In a specific workflow where contours are edited (enlarged, moved, copied,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sagittal Blade 18.0X0.97X90MM Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling the Sagittal Blade...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2016· Microgenics Corporation

Recalled Item: Thermo Scientific QMS Everolimus Assay Recalled by Microgenics Corporation...

The Issue: A reagent stability issue (still under investigation) causes less separation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2016· Pentax of America Inc

Recalled Item: Pentax Video Colonoscope is intended to be used with a Recalled by Pentax of...

The Issue: Pentax is initiating the product correction of several model numbers of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2016· Prismatik Dentalcraft, Inc

Recalled Item: BruxZir Shaded Recalled by Prismatik Dentalcraft, Inc Due to Prismatik...

The Issue: Prismatik Dentalcraft is recalling BruxZir Shaded because the new design was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2016· Pentax of America Inc

Recalled Item: Pentax Video Gastroscope is intended to be used with a Recalled by Pentax of...

The Issue: PENTAX Medical is initiating this field action to provide customers that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...

The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Novarad Corporation

Recalled Item: NovaPACS versions 8.4.7 Recalled by Novarad Corporation Due to Novarad...

The Issue: Novarad Corporation announces a voluntary field action for the NovaPACS...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...

The Issue: 78 Viva CRT -Ds and Evera ICDs that were manufactured with a specific subset...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Philips Electronics North America Corporation

Recalled Item: PCR Compano Basic Reader using 100-127V as mains voltage. Model numbers:...

The Issue: A defect component of the Compano reader power supply can cause the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Merit Medical Systems, Inc.

Recalled Item: Custom Fluid Management Set Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for Fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Maquet Cardiovascular Us Sales, Llc

Recalled Item: The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a...

The Issue: Post Market Surveillance cases reported to Maquet showing instances in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2016· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab 1240 Blood Gas Analyzer Siemens Material Number (SMN):...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products URIC Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products LAC Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 405 Blood Gas Analyzer nBili Siemens Material Number...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDLab 1265 Blood Gas Analyzer Siemens Material Number (SMN): 10321852...

The Issue: There is a potential for the first and/or last name of one patient to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products GLU Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed that N-Acetylcysteine (NAC), a drug...

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

Class II — Potential Health HazardOngoing