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. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 24421–24440 of 27,157 recalls
Recalled Item: CATH PACK Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH TRAY Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument Sternal Zip Flex System intended for use...
The Issue: When using the 1st generation Zip Fix Application Instrument it is possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (6 units) Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (1 unit) Recalled by Codman & Shurtleff, Inc. Due to Drug flow...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens EasyLink Informatics System V4.0/V5 Siemens Recalled by Siemens...
The Issue: May not perform as intended under certain conditions, causing the release of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cypher MIS Screw System Recalled by Ebi, Llc Due to Several complaints were...
The Issue: Several complaints were reported to exhibit screw head splay in the Cypher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon 14 Microbore Extension Set with Bionector Recalled by Churchill...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Dressing Change Kit Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Surgical Eye Spears Recalled by DeRoyal Industries Inc Due to...
The Issue: One lot of eye spears was labeled as being x-ray detectable, but contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T8 REMOVAL HEAD Recalled by Medtronic Sofamor Danek USA Inc Due to One lot...
The Issue: One lot of the T8 Removal Head had incorrect hardness specification, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120/2120i Hematology Systems with ADVIA Autoslide connected to it...
The Issue: Siemens determined that if an autosampler rack jam error occurs during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular...
The Issue: Due to a labeling error related to the conversion of the inner diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for...
The Issue: Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.