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. 2,506 recalls have been distributed to Alaska in the last 12 months.
Showing 10581–10600 of 46,762 recalls
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAJUNK Continuous Epidural Tray Recalled by Pajunk Medical Systems, L.P. Due...
The Issue: The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use Recalled...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octreotide Acetate Injection 500 mcg/mL Recalled by Viatris Inc Due to...
The Issue: Presence of Particulate Matter: Product complaint for the presence of glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V...
The Issue: Batteries could become unstable when not properly maintained and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quinapril and Hydrochlorothiazide Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...
The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...
The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fondaparinux Sodium Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Subpotent Drug: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pyridostigmine Bromide Oral Solution Recalled by VistaPharm, Inc. Due to...
The Issue: cGMP Deviations: Out of specification for assay of one of the preservative...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flunisolide Nasal Solution Recalled by Ingenus Pharmaceuticals Llc Due to...
The Issue: Out of specification for related substances (impurities).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is an incorrect manufacturing date/timestamp within the software which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.