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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 22341–22360 of 46,762 recalls
Recalled Item: Monsel's (Ferric Subsulfate) Solution Recalled by Gordon Laboratories Due to...
The Issue: Superpotent Drug: contains higher levels of Iron than labeled.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soothe & Cool Protect Moisture Guard Skin Protectant (petrolatum 59%)...
The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Absorica (Isotretinoin) Capsules 30 mg USP Recalled by Sun Pharmaceutical...
The Issue: Subpotent Drug: Isotretinoin content results were lower than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocortisone Cream 1% MS Anti itch Cream with Intensive Healing 2 oz tubes...
The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%)...
The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK STEM with Microporous Surface MP Reconstruction Prosthesis Recalled by...
The Issue: The reaming guide and the guide rod can't be screwed into the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN):...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number Recalled by...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN):...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Planetary Herbals Mullein Lung Complex Recalled by Threshold Enterprises Ltd...
The Issue: Recall of Mullein Lung Complex due to a labeling error which indicates the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Levoxyl (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...
The Issue: Superpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vygon DUALSTOP Red Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Adapter Percutaneous Pin Recalled by Medtronic Navigation, Inc....
The Issue: Under certain circumstances, the percutaneous pin adapter used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VisuMax Software Version 2.10.13 with activated Software-Module ReLEx...
The Issue: VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature...
The Issue: Some SureStep" Foley Tray Systems with product catalog number A319418AM and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vyon DUALSTOP White Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-View¿ Contrast Enhanced Digital Mammography Recalled by Hologic, Inc. Due...
The Issue: Calibration issue not possible to visualize contrast uptake in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.