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. 2,433 recalls have been distributed to Vermont in the last 12 months.
Showing 13941–13960 of 27,157 recalls
Recalled Item: ARIES GBS Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Extraction Kit Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Group A Strep Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aries Bordetella Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive...
The Issue: Deterioration of C-reactive protein (CRP) reagent in Optilite C-Reactive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...
The Issue: The product contains a misprinted expiration date on the peel pack. Both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: 722001 Allura Xper Recalled...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...
The Issue: Potential for the sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...
The Issue: The polarity of the output of power supply was reversed. Due to polarity of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...
The Issue: Complaints received that products packaged with the incorrect introducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...
The Issue: The devices were released from a lot for which one sample failed to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.