Recalls affecting Vermont
Notices that name Vermont in their distribution area, plus every nationwide recall — nationwide recalls reach Vermont too.
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Class II · 2 months ago
Tobii Dynavox Llc TD Navio Maxi Speech Generating Device Model/ recall: Under certain conditions, the battery mounting tabs may become damaged
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading…
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Class II · 2 months ago
Beckman Coulter DxC 500i Clinical Analyzer Modules using software recall: a software defect in which the Parameter Package (PP) import logic overwrites
a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously…
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Class II · 2 months ago
Gentherm Medical, LLC Innercool Coolblue Console, Model STx recall: Overheating of the 115V CPU board may cause the device to shut down
Overheating of the 115V CPU board may cause the device to shut down.
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Class II · 2 months ago
Fort Defiance Industries recall: The Automated Field Steam Sterilizer's water recovery system 120V Amphenol
The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which…
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Class II · 2 months ago
Gentherm Medical, LLC Blanketrol III, Model 233 recall: Overheating of the 115V CPU board may cause the device to shut down
Overheating of the 115V CPU board may cause the device to shut down.
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Class I · 2 months ago
Boston Scientific Enroute Transcarotid Neuroprotection System recall: Potential for arterial sheath tip separation or partial tip separation during
Potential for arterial sheath tip separation or partial tip separation during use.
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Class II · 2 months ago
Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software recall: a software defect in which the Parameter Package (PP) import logic overwrites
a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously…
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Class I · 2 months ago
Boston Scientific Enroute Transcarotid Neuroprotection System Plus recall: Potential for arterial sheath tip separation or partial tip separation during
Potential for arterial sheath tip separation or partial tip separation during use.
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Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
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Class II · 2 months ago
Siemens Healthineers Immulite 2000 Systems SYP recall: Syphilis Screen assay may contain a negative patient bias resulting in low
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
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Class II · 2 months ago
ConvaTec, Inc Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703 recall: Urostomy Pouches may leak from cap during use
Urostomy Pouches may leak from cap during use.
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Class II · 2 months ago
Philips North America Llc Cardiac Workstation 7000. Product Number: 860441 recall: Device will intermittently provide inaccurate data related to native heart
Device will intermittently provide inaccurate data related to native heart rate.
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Class II · 2 months ago
Covidien, LLC EndoFlip System that includes: Endoflip 1 System EF-100 05391530810050 recall: The system's 24-hour usage limit results in catheters incorrectly flagged
The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
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Class III · 2 months ago
Paragon 28, Inc. Custom Made Device Implant 6123 Navicular Cage Small Right Rev recall: Device was recalled due to an elevated oxygen level in excess
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material…
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Class II · 2 months ago
Boston Scientific Corporation Suture Cinch Long 1pk. Endoscopic tissue approximation recall: Device may fail to deploy the cinch implant and/or fail to cut the suture
Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.
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Class II · 2 months ago
Siemens Healthineers Immulite 2000 Systems SYP recall: Syphilis Screen assay may contain a negative patient bias resulting in low
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
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Class II · 2 months ago
Philips North America Llc Cardiac Workstation 5000. Product Number: 860439 recall: Device will intermittently provide inaccurate data related to native heart
Device will intermittently provide inaccurate data related to native heart rate.
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Class II · 2 months ago
Foundation Medicine, Inc. Hamilton Microlab STAR Liquid Handler recall: Software issue that can cause an increase in spontaneous software closures
Software issue that can cause an increase in spontaneous software closures.
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Class II · 2 months ago
Tobii Dynavox Llc TD Navio Midi Speech Generating Device Model/ recall: Under certain conditions, the battery mounting tabs may become damaged
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading…
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Class II · 2 months ago
Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System recall: Due to a firmware defect, the portable organ transfer device datalogger
Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed…
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Class II · 2 months ago
Siemens Healthcare Diagnostics, Inc. Syva EMIT 2000 Quinidine Assay REF: 4Q019UL recall: Due to unacceptable precision performance exhibited in certain lots
Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated…
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Class II · 2 months ago
restor3d Inc. Brand Name: Veritas Standard Reverse Total Shoulder Product Name recall: Due to incorrect machining of peripheral screw hole resulting in potential
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
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Class II · 2 months ago
Gentherm Medical, LLC Blanketrol II Model 222S recall: Overheating of the 115V CPU board may cause the device to shut down
Overheating of the 115V CPU board may cause the device to shut down.
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Class II · 2 months ago
Siemens Healthcare Diagnostics, Inc. Beckman Coulter recall: Due to unacceptable precision performance exhibited in certain lots
Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated…