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. 2,440 recalls have been distributed to Alaska in the last 12 months.
Showing 15201–15220 of 27,254 recalls
Recalled Item: TomoSPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-SPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by Bard Medical Division...
The Issue: An improper wiring connection on the chiller assembly may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...
The Issue: Incorrect use-by date on the device registration/patient file labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...
The Issue: The incorrect plastic was used to manufacture the handles of these shears,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...
The Issue: In 2018, Philips Respironics added foam replacement to the preventive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...
The Issue: Device could not meet the requirements for systolic pressure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...
The Issue: There is a potential risk of electrical fire when fluid leaks into the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper Product Usage: Vascular Recalled by Philips Healthcare Due to...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ Product Usage: Vascular Recalled by Philips Healthcare Due to The first...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.