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. 2,333 recalls have been distributed to Alaska in the last 12 months.
Showing 32361–32380 of 46,762 recalls
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...
The Issue: The software did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...
The Issue: Cut lines on the image may present horizontally rather than vertically.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: If a reader selects Multi-study review prior to the original study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...
The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...
The Issue: Eye Station images were not importing properly and were imported under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...
The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....
The Issue: There is a potential connection issue when powering up the Merge Hemo Record...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...
The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...
The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...
The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine 75 mg Tablet Recalled by Bryant Ranch Prepack Inc. Due to...
The Issue: Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection USP Recalled by B. Braun Medical Inc Due to...
The Issue: Non-Sterility: fungal contamination due to leaking containers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.