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 1416114180 of 46,762 recalls

Medical DeviceAugust 3, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...

The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Luminex Corporation

Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...

The Issue: There is potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Olympus Corporation of the Americas

Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...

The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2021· Je Dois Lavoir LLC

Recalled Item: 365 SKINNY High Intensity Capsules Recalled by Je Dois Lavoir LLC Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 2, 2021· Akorn, Inc.

Recalled Item: Artificial Tears Ointment Recalled by Akorn, Inc. Due to Non-Sterility - OOS...

The Issue: Non-Sterility - OOS sterility testing observed during 12-month controlled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2021· Macleods Pharma Usa Inc

Recalled Item: Clopidogrel Tablets Recalled by Macleods Pharma Usa Inc Due to Presence of...

The Issue: Presence of foreign matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...

The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· GE Healthcare, LLC

Recalled Item: Flow sensors that may be installed in the following GEHC Recalled by GE...

The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uMI 550 System - Product Usage: intended to be operated Recalled by Shanghai...

The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· GE Healthcare, LLC

Recalled Item: Flow sensors kept as stand-alone user replaceable spare parts for Recalled...

The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES Recalled by...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Bag Access Device Recalled by CAREFUSION Due to Needle-free...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite 'Y' Extension Set 2 Needle-Free Valves Recalled by CAREFUSION...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED Recalled...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite Recalled by CAREFUSION Due to Needle-free connector valves,...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing