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. 2,369 recalls have been distributed to Vermont in the last 12 months.
Showing 19081–19100 of 27,157 recalls
Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...
The Issue: Inability to deploy the stent or partial stent deployment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...
The Issue: Inability to deploy the stent or partial stent deployment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...
The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...
The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...
The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5 Recalled by Volcano Corporation Due to Volcano has become aware...
The Issue: Volcano has become aware of an incompatibility issue between Impacted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT S(20) - 4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: The bracket that is used to lift the cover has bolts that were not welded in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: The bracket that is used to lift the cover has bolts that were not welded in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.