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. 1,968 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,968 in last 12 months

Showing 48214840 of 46,762 recalls

Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 7.5CPM Recalled by Alcon Research LLC Due to Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY INTREPID SB Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Omnia Medical

Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...

The Issue: Failure of fusion system instruments in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Omnia Medical

Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...

The Issue: Failure of fusion system instruments in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB Recalled by Alcon...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ TTL PLUS VPAK 20000CPM BWV Model/Catalog Number: Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE2.75MM AN...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys. This anesthesia gas machine is intended to provide general Recalled...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys CS2 with Et Control. This anesthesia gas machine is Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Meddev Corp

Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...

The Issue: Due to mislabeling of products

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Meddev Corp

Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...

The Issue: Due to mislabeling of products

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Intuitive Surgical, Inc.

Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...

The Issue: There is a potential that the robotic system's instrument cart arm may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 100. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing