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. 2,299 recalls have been distributed to Alaska in the last 12 months.
Showing 38421–38440 of 46,762 recalls
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...
The Issue: Internal testing and investigation of the packaging revealed cracks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items...
The Issue: The blade retaining clip may be difficult to engage and thereby increase the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets Recalled by...
The Issue: Tubing may detach at the connect/disconnect location on the MiniMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...
The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....
The Issue: Alcon is conducting a medical device recall due to the possible presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Subpotent Drug: Heparin raw material was found to have low potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...
The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM...
The Issue: The 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...
The Issue: Portions of the lots may contain units with an incorrect lens axis condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...
The Issue: It was determined that if the Mammomat Inspiration system is not secured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Macadamia nuts in various formats: (1.) Western Family Macadamia Diced Nuts...
The Issue: Macadamia nuts may have possible contamination with Salmonella florida.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chicken flavored broth base and seasoning Recalled by Kent Precision Foods...
The Issue: Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...
The Issue: Potential breach of sterile barrier due to defective product tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...
The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...
The Issue: Drill set may contain incorrect drill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.