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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 31161–31180 of 46,762 recalls
Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...
The Issue: Product gives incorrect low blood glucose levels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...
The Issue: Product gives incorrect low blood glucose levels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...
The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit Select Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical...
The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Recalled...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe Recalled by...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece only Recalled by ConMed Corporation Due to The...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set Recalled by ConMed...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe Recalled by ConMed...
The Issue: The packaging seal may contain a crease. The crease may result in an open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to Recalled by Cardinal...
The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...
The Issue: Superpotent drug: Out of specification test result for assay during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II. Recalled...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II. Recalled by The...
The Issue: There was a potential for the Adaptor and Light Adaptor for Small Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.