Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 27141–27157 of 27,157 recalls
Recalled Item: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To...
The Issue: The outer jacket is receding away from the black sensor prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT Link Waterbath Recalled by Dako North America Inc. Due to Dako is...
The Issue: Dako is recalling the PT Link Waterbath because of a possible electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba CT systems Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: The systems all have a similar table control board. It has been found that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics...
The Issue: The power to the Esprit Display's Backlight is interrupted, causing the GUI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HiRes 90K devices with Helix Electrodes Model CI 1400-02H The Recalled by...
The Issue: Advanced Bionics is recalling the the HiRes 90K cochlear implant with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC MiniView 6800 Mobile Recalled by GE OEC Medical Systems, Inc Due to...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to Please be aware...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Plus Digital Recalled by GE OEC Medical Systems, Inc Due to Please...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cannulaide Recalled by Beevers Manufacturing & Supply, Inc. Due to...
The Issue: Cannulaide model CA 101 was recalled because the firm discovered this model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: No packaging. The device is a computed tomography scanner. Intended Recalled...
The Issue: When the Extended Display Firled ov View reconstruction is used, the CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile...
The Issue: Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 8800 Flexview Recalled by GE OEC Medical Systems, Inc Due to Please be...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC InstaTrak 3500 Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaTrak with Multiple Dataset Navigation Recalled by GE OEC Medical...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT System 6/10/16/16P/40 configuration. No packaging Recalled by...
The Issue: The system has a gap that can appear between the upper and lower tilt stand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUN|DASH RADIUS 252 tanning system Recalled by JK Products & Services, Inc...
The Issue: The firm has tracked a systematic failure in the door cord on the Sun|Dash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Prisma 2K Hearing Aid Product Usage: A behind the Recalled by...
The Issue: Siemens became aware of an issue where an infant or child could open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.