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 29012920 of 46,762 recalls

Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 3 Month Trial Tampon Box Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 18 Coated Super and 18 Nude Super Tampons Recalled by DAYE...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product lacks...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 9 Coated Regular and 9 Coated Super Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 9 Coated Regular Tampons and 9 Nude Regular Tampons Recalled by DAYE (ANNE'S...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· Oridion Medical 1987 Ltd.

Recalled Item: Microstream Instructions for Use and Part Number used with - Product...

The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...

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

Class II — Potential Health HazardOngoing
FoodFebruary 15, 2025· NATURIPE VALUE ADDED FRESH LLC

Recalled Item: Berry Buddies Recalled by NATURIPE VALUE ADDED FRESH LLC Due to Undeclared...

The Issue: Incorrect back label on product resulting in undeclared allergens (wheat, eggs)

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2025· Abbott Medical

Recalled Item: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...

The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2025· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear 1mL Applicators Recalled by CareFusion 213, LLC Due to...

The Issue: Non-Sterility: contamination of Aspergillus penicillioides, due to breach in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Modular Stem cylindrical Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: A problem was discovered during the scanning process of the outer carton...

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

Class II — Potential Health HazardOngoing