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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1386113880 of 27,254 recalls

Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2019· Molnlycke Health Care, Inc

Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...

The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Hamilton Medical AG

Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...

The Issue: New software version for affected ventilators reduces the probability of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Premium Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Vision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Precision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Lightning Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing