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. 2,487 recalls have been distributed to Alaska in the last 12 months.
Showing 12561–12580 of 46,762 recalls
Recalled Item: PALIPERIDONE EXTENDED-RELEASE TABLETS Recalled by The Harvard Drug Group Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NanoSight LM10 fitted with LM12 module. A laboratory instrument for Recalled...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoSight LM10 fitted with LM14 module. A laboratory instrument for Recalled...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL Recalled by Medtronic...
The Issue: There is a software anomaly with the InterStim X Clinician software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V680 Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Universal Flexible Arm part number Recalled by Integra LifeSciences...
The Issue: Excess force used to tighten the Universal Flexible Arm can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical, Inc. Due to...
The Issue: Lack of sterility assurance: leaking bags
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DigitalDiagnost C50 1.1 Recalled by Philips North America Llc Due to...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Application software VE20 (Material Number 10848815) installed on the...
The Issue: After CT image data from Toshiba is loaded, image mirroring can occur along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor in combination with a Siemens Healthineers table Recalled...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane- in combination with a Siemens Healthineers table...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- in combination with a Siemens Healthineers table or Recalled by...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: Product is mislabeled as self-righting Luer slip tip caps, yellow.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anterior Hip Pack - Surgical Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coryell Memorial Hosp Total Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicare Neuro Pack - Neurological Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Pack - Surgical Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lum Lam Custom Pack - Anesthesia Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.