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. 2,295 recalls have been distributed to Vermont in the last 12 months.
Showing 38601–38620 of 47,027 recalls
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED ADULT R2 Multifunction Electrodes Recalled by ConMed Corporation Due...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and...
The Issue: Breakage of the nut that secures the heater head in place, which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Max Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...
The Issue: Internal testing and investigation of the packaging revealed cracks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets Recalled by...
The Issue: Tubing may detach at the connect/disconnect location on the MiniMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items...
The Issue: The blade retaining clip may be difficult to engage and thereby increase the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile drape Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...
The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Subpotent Drug: Heparin raw material was found to have low potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....
The Issue: Alcon is conducting a medical device recall due to the possible presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.