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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 641–660 of 27,254 recalls
Recalled Item: IntelliVue Multi-Measurement Module X3. Product Number: 867030. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX550. Product Number: 866066. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX750. Product Number: 866471. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OER-Mini Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX450. Product Number: 866062. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP70. Product Number: M8007A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO BrainPath Recalled by Stryker Corporation Due to Tape used to secure...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...
The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn INF BAG Recalled by Baxter Healthcare Corporation Due to...
The Issue: Replacement bladder kit for the Welch Allyn two-piece reusable blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Kits/ containing flow cells Recalled by Illumina, Inc. Due to An...
The Issue: An instrument intended for sequencing DNA libraries with in vitro diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PERFUSION SYRINGE Recalled by Medline Industries, LP Due to Medline...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis System Recalled by Nipro Medical Corporation Due to Screw may...
The Issue: Screw may loosen or fallout of Hemodialysis system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2...
The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.