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 14521–14540 of 27,157 recalls
Recalled Item: B20i Patient Monitor and B20i V2 Patient Monitor. The device Recalled by GE...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROCARE B20 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...
The Issue: Patient monitors may restart due to network overload caused by network...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiLite X-Short anti-tip tubes Recalled by TiSport, Llc Due to The anti-tip...
The Issue: The anti-tip tubes potentially fail in certain situations and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...
The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...
The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...
The Issue: Potential for outer pouch sterile barrier to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME)...
The Issue: Firm identified an issue in the manufacturing process which might contribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...
The Issue: Bayer has received reports of loose particulate in the filter when the dust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Hemi-Artery Recalled by CryoLife, Inc. Due to The...
The Issue: The conduit length and branch length of a SG Pulmonary Hemi-Artery were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altrix¿ Precision Temperature Management System Model: 8001Product Usage:...
The Issue: Users may experience alarm fatigue due to frequent alarming relating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is Recalled by...
The Issue: Product may not meet the internal manufacturing shaft subassembly burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Recalled by BioFire...
The Issue: Increased risk of false positive results for Proteus when the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of...
The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Omega System Recalled by Alpha Omega Engineering Due to If cables are...
The Issue: If cables are improperly connected, current may reach high charge density,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.