Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,576 recalls have been distributed to Idaho in the last 12 months.
Showing 8841–8860 of 27,833 recalls
Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR Recalled by SEDECAL SA Due to While cleaning or...
The Issue: While cleaning or disinfecting the system, if the process is not followed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: These are communication systems Recalled by Hill-Rom Inc. Due to An...
The Issue: An unrecoverable error may occur where a component will fail to complete the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPL Coupling Gel Recalled by Lumenis, Inc. Due to Ultrasound gels and...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 Recalled by...
The Issue: When the ultrasound system is used in combination with a Fujifilm (formally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skinny Needle with Chiba Tip. RPN 090010 Recalled by Cook Inc. Due to...
The Issue: Specific lots may contain black debris on the exterior of the inner stylet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL ReadiPlasTin (20 mL) Recalled by Instrumentation Laboratory Due to...
The Issue: The firm has received customer reports of performance issues with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion kits Recalled by Medtronic Perfusion Systems Due...
The Issue: Product is labeled as non-pyrogenic but endotoxin testing was not performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno with software VE20C- diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane with software VE20C-diagnostic imaging angiography...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor with software VE20C-diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager application software (D00U005)...
The Issue: The processing of collected episode data may fail due to a software error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affected components are limited to the Monoprice charging cable (Product...
The Issue: Warning Added: Using damaged cables or chargers, or charging when moisture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.