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. 2,503 recalls have been distributed to Vermont in the last 12 months.
Showing 7481–7500 of 27,157 recalls
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001...
The Issue: Drill Pin (drill bit) is not compatible with the Drill Template included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filter + Catheter Mount Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S with Expandi-Flex/Elbow: a) Recalled by TELEFLEX LLC Due...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR Power Knee OSSUR Power Knee Recalled by Ossur Americas Due to Battery...
The Issue: Battery may dislodge from the Power Knee
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BiPAP A30 Recalled by Philips Respironics, Inc. Due to Motor...
The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BiPAP V30 Auto Recalled by Philips Respironics, Inc. Due to Motor...
The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips OmniLab Advanced+ Intl (Flow Gen) Recalled by Philips Respironics,...
The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips OmniLab Advanced + with Heated Tube Humidifier Recalled by Philips...
The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BiPAP A40 Recalled by Philips Respironics, Inc. Due to Motor...
The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips OmniLab Advanced+ Recalled by Philips Respironics, Inc. Due to Motor...
The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...
The Issue: The outer sterile package cavity has a corner wall thickness that is below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.