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. 2,283 recalls have been distributed to Alaska in the last 12 months.
Showing 41861–41880 of 46,762 recalls
Recalled Item: ADVIA Centaur Intact PTH Calibrator (6 pack) Recalled by Siemens Healthcare...
The Issue: PTH Calibrator packaged with only high calibrator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile Recalled...
The Issue: Issues with the Ingenuity TF PET/CT Software Version 4.0 could pose a risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Equipment Management System Recalled by Steris Corporation Due to...
The Issue: Dr¿ger Medical GmbH has notified STERIS of the potential for a break in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: The manufacturer has conducted a review of the results of product testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO - Beam shaping block for Radiation Therapy. Recalled by Elekta,...
The Issue: Clinical mistreatment may occur when there are errors in the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particulate embedded in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride 2% and Epinephrine 1:100 Recalled by Novocol...
The Issue: Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEART CATH CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH TRAY Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH PACK Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.