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.
Showing 14221–14240 of 46,762 recalls
Recalled Item: Alprostadil Injection USP Recalled by Teva Pharmaceuticals USA Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vecuronium Bromide for Injection 10 mg Recalled by Teva Pharmaceuticals USA...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethosuximide Oral Solution USP 250 mg/5 mL Recalled by PAI Holdings, LLC....
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cimetidine Hydrochloride Oral Solution 300 mg/5 mL Recalled by PAI Holdings,...
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...
The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...
The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...
The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...
The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...
The Issue: Missing splash guard which may expose users to hazardous materials. .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX Delta Mod Head Recalled by Corin Ltd Due to The packaging...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.