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. 2,550 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,550 in last 12 months

Showing 721740 of 27,254 recalls

Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kit Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia circuit kit Recalled by Medline Industries, LP Due to Firm...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2025· C-RAD POSITIONING AB

Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...

The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Myofunctional Research Company USA

Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...

The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Recalled...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing