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. 2,517 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,517 in last 12 months

Showing 69416960 of 46,762 recalls

Medical DeviceNovember 20, 2023· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...

The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 - IVD For use as a Recalled by Randox Laboratories...

The Issue: Target for Alkaline Phosphatase (ALP) for the AMP optimized to IFCC 37¿C...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...

The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Medtronic Inc.

Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...

The Issue: Seal defects could compromise the ability of the product packaging to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ROi CPS LLC

Recalled Item: Regard Dressing change kit Recalled by ROi CPS LLC Due to ROi CPS...

The Issue: ROi CPS manufactured and distributed medical convenience kits with an...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· Keystone Industries

Recalled Item: KeySplint Hard Clear - Indicated for the fabrication of orthodontic Recalled...

The Issue: Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirTouch F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirTouch N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F30 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit N10 Nasal Masks and User Guide Recalled by ResMed Ltd. Due to Masks...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F20 Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit F30i Full Face Mask and User Guide Recalled by ResMed Ltd. Due to...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· ResMed Ltd.

Recalled Item: AirFit N20 Nasal Mask and User Guide Recalled by ResMed Ltd. Due to Masks...

The Issue: Masks non-invasive interface for channeling airflow to patients have magnets...

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

Class I — Serious Health HazardOngoing
FoodNovember 17, 2023· The HMC Group Marketing Inc

Recalled Item: HMC Farms Nectarines 2lb Gusset Bag Recalled by The HMC Group Marketing Inc...

The Issue: Potential contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 17, 2023· The HMC Group Marketing Inc

Recalled Item: HMC Farms Peaches 2lb Gusset Bag Recalled by The HMC Group Marketing Inc Due...

The Issue: Potential contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 17, 2023· The HMC Group Marketing Inc

Recalled Item: HMC Farms White Nectarines 2lb Gusset Bag Recalled by The HMC Group...

The Issue: Potential contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 17, 2023· The HMC Group Marketing Inc

Recalled Item: HMC Farms White Peaches 4lb box Recalled by The HMC Group Marketing Inc Due...

The Issue: Potential contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 17, 2023· The HMC Group Marketing Inc

Recalled Item: HMC Farms Nectarines 4lb bag Recalled by The HMC Group Marketing Inc Due to...

The Issue: Potential contamination with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund