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. 2,541 recalls have been distributed to Vermont in the last 12 months.
Showing 2281–2300 of 27,157 recalls
Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...
The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...
The Issue: Potential that the induction seal is not completely sealed to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...
The Issue: Due to manufacturing issue (unintended by-product of the injection molding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...
The Issue: Product complaints were received describing the A820 myPTM app taking longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number:...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK Recalled...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Software...
The Issue: Software issues could potentially result in: 1) delays in accessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MSOT Acuity Echo is a Class 4 medical laser Recalled by Ithera Medical...
The Issue: The MSOT Acuity Echo does not include an adequate instruction for safe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Labeling...
The Issue: Labeling is insufficient regarding delays in access to medication. The firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a Recalled by...
The Issue: Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6....
The Issue: Sysmex was made aware of a report of false results due to carry-over caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E...
The Issue: It was identified internally that two commingle events occurred where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C...
The Issue: It was identified internally that two commingle events occurred where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irix-A Integrated Lumbar Fusion System Recalled by XTANT Medical Holdings,...
The Issue: Certain implants in the Irix-A Lumbar Fusion System were distributed while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.