Recalls affecting West Virginia
Notices that name West Virginia in their distribution area, plus every nationwide recall — nationwide recalls reach West Virginia too.
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Class II · 11 months ago
Remel, Inc 1. Camhb W/LHB, Manual, 11ML, 10/BOX YCP112-10 2. Brucella Broth recall: Products may contain contamination, which may result in a darker or brown
Products may contain contamination, which may result in a darker or brown media color.
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Class II · 11 months ago
Stryker Corporation NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination recall: Tape used to secure components within packaging contains latex
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an…
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Class II · 11 months ago
Pivotal Health Solutions, Inc. Quantum Intersegmental Table, Model/ recall: The heat function may become damaged over time due to patients pressing
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to…
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Class II · 11 months ago
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system recall: The motorized longitudinal movement of the FlexArm stand may be inconsistent
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to…
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Class II · 11 months ago
Medtronic Sofamor Danek USA Inc Catalyft PL & PL40 recall: Expandable interbody system cage may loose height or collapse (loss
Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological…
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Class II · 11 months ago
Intelerad Medical Systems Incorporated IntelePACS - InteleConnect / TechPortal recall: Software application that receives digital images and data
Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that…
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Class II · 11 months ago
Magellan Diagnostics, Inc. The LeadCare¿ II Blood Lead Test System relies recall: Calibration Buttons being used in the kitting process were incorrectly
Calibration Buttons being used in the kitting process were incorrectly labeled as Lot 2323M for lot 2333M. The use of mislabeled calibration Button…
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Class II · 11 months ago
Brand Name: Evis Exera III Duodenovideoscope Product Name: Olympus recall: Continued reports of positive cultures and infections have identified updates
Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF…
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Class II · 11 months ago
Djo, LLC Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder recall: The IFU (Information for Use) on the wrap instructs the user to heat the hot
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may…
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Class II · 11 months ago
Pivotal Health Solutions, Inc. Quantum Intersegmental Table, Model/ recall: The heat function may become damaged over time due to patients pressing
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to…
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Class II · 11 months ago
FoundationOne Liquid CDx , TECH-0009 version 6.0 recall: Reports were sent to customers without the companion diagnostic (CDx) Claims
Reports were sent to customers without the companion diagnostic (CDx) Claims Page. Claims pages were distributed via amended reports within 7 days of…
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Class II · 11 months ago
Alcon Research LLC Constellation Ultravit 10K and Constellation Hypervit 20K recall: XXX
XXX
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Class II · 11 months ago
Mindray North America Isoflurane V90 Electronic Vaporizer with the A9 Anesthesia recall: Potential for anesthesia leakage
Potential for anesthesia leakage.
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Class II · 11 months ago
Medtronic MiniMed, Inc. CareLink Clinic, REF: MMT-7350 recall: Software error causing incorrect data to be displayed on the 24-hour Sensor
Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based…
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Class II · 11 months ago
Straumann USA LLC Emdogain recall: The possibility for this product that is intended for demonstration purposes
The possibility for this product that is intended for demonstration purposes only to be placed in patients.
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Class II · 11 months ago
Argon Medical Devices, Inc Option"Elite Vena Cava Filter System REF 352506070E Udi-Di recall: Due to complaints of increased resistance when advancing the dilator within
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural…
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Class II · 11 months ago
Stryker Corporation NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 recall: Tape used to secure components within packaging contains latex
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an…
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Class II · 11 months ago
Mindray North America Sevoflurane V90 Electronic Vaporizer with the A9 Anesthesia recall: Potential for anesthesia leakage
Potential for anesthesia leakage.
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Class II · 11 months ago
Stryker Corporation NICO BrainPath recall: Tape used to secure components within packaging contains latex
Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an…
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Class II · 11 months ago
Cepheid Xpert MTB/RIF recall: Product testing did not meet expected stability criteria
Product testing did not meet expected stability criteria.
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Class II · 11 months ago
FoundationOne CDx , RAL-0003 version 31.0 recall: Reports were sent to customers without the companion diagnostic (CDx) Claims
Reports were sent to customers without the companion diagnostic (CDx) Claims Page. Claims pages were distributed via amended reports within 7 days of…
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Class II · 11 months ago
Noah Medical Corporation Brand Name: Galaxy System Product Name: Galaxy System Model/ recall: Due to Users not having access to the Instructions for Use/User Manual
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
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Class II · 11 months ago
Medical Products Laboratories, Inc. Walgreens Saline Nasal Spray With Xylitol recall: Microbial contamination of a non-sterile product - microorganism found
Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
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NHTSA safety recall · 11 months ago
Chrysler recall: A software error may cause the instrument panel cluster display to be blank
A software error may cause the instrument panel cluster display to be blank. As such, these vehicles fail to comply with the requirements of Federal…