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 34841–34860 of 47,027 recalls
Recalled Item: Midazolam (PF) 0.1 mg/mL in 0.9% Sodium Chloride Recalled by Pharmakon...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine 100 mg/mL Recalled by Pharmakon Pharmaceuticals Due to Stability...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine (PF) 100 mcg/mL in 0.9% Sodium Chloride Recalled by Pharmakon...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ephedrine Sulfate 5 mg/mL in 0.9% Sodium Chloride Recalled by Pharmakon...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine 50 mg/mL Recalled by Pharmakon Pharmaceuticals Due to Stability...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Provocholine Pre-diluted Set II in 0.9% Sodium Chloride Recalled by...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software and firmware bugs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...
The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...
The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...
The Issue: Some devices exhibit backup VVI operation due to a backup reset.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...
The Issue: patient procedure interruption due to a potential system failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....
The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution Recalled by Bausch & Lomb, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cevimeline Hydrochloride Capsules Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Stability Specifications: product may not meet specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.