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.
Showing 6701–6720 of 27,254 recalls
Recalled Item: Amicus Exchange Kit Therapeutics. Component of Amicus Separator...
The Issue: Potential for centrifuge packs to develop a stress leak for certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus MNC Apheresis Kit Double Needle. Component of Amicus Separator...
The Issue: Potential for centrifuge packs to develop a stress leak for certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Global Total LP single step medium Recalled by CooperSurgical, Inc. Due to...
The Issue: It has come to CooperSurgical's attention that the affected Product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to Firm has...
The Issue: Firm has initiated a removal of the product due to insufficient evidence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DreamStation Auto BiPAP and CPAP Recalled by Philips Respironics,...
The Issue: A limited number of remediated Philips DreamStation units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed 7.0 Recalled by...
The Issue: Due to potential leaks associate with the Oral/Nasal Tracheal Tube Cuffed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II ROODRA non-invasive vascular diagnostic device Recalled...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II REVO non-invasive vascular diagnostic device Recalled by...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 App Recalled by Abbott Diabetes Care, Inc. Due to If using...
The Issue: If using affected glucose monitoring app on Android 13 Operating System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal SafeLiner Suction Canister Recalled by DeRoyal Industries Inc Due to...
The Issue: The reason for the voluntary recall is due to shrinkage of the canister lid....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton DBF Inject: a) GRAFTON T50303 DBF INJECT 3CC Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Matrix: a) DBM S42200 GRAFTON 2.5CMX10CM 2EA MATRIX...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Crunch a) DBM S44105 GRAFTON 5CC CRUNCH Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic XPANSE Bone Insert: a) DBM T600106 XPANSE SMALL-C 6 Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Gel: a) DBM S41120 GRAFTON GEL 1CC Recalled by Medtronic...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.