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. 2,614 recalls have been distributed to Idaho in the last 12 months.
Showing 1901–1920 of 27,833 recalls
Recalled Item: DORO¿ Easy-Connect Navigation Adaptor Recalled by Pro-Med Instruments Gmbh...
The Issue: Potential of compromised compatibility resulting in influence on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Update to IFU...
The Issue: Update to IFU to provide additional information related to risk with device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Update to IFU...
The Issue: Update to IFU to provide additional information related to risk with device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate Mobile Power Unit: Recalled by Thoratec LLC Due to Left...
The Issue: Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number:...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Recalled by...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK (Name Recalled by CareFusion 303, Inc. Due to Users trying...
The Issue: Users trying to restock a single bin location of an automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 4 Fr Single-Lumen PowerPICC Catheters Recalled by Bard Access Systems,...
The Issue: Catheters indicated for short-or-long term access to the central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower Recalled by CareFusion...
The Issue: Due to a software bug, automated dispensing cabinet is unable to calculate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Revised C Reactive Protein (RCRP) Recalled by Siemens Healthcare...
The Issue: Incorrect software flagging may occur for the assay that may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...
The Issue: Nerve Monitoring System with certain software versions has potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...
The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...
The Issue: The devices are missing the laser marked depth markings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.