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International Medical Devices Database
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Recall of TITI GLOVE, Latex Examination Gloves, Size: Large
According to National Organization for Medicines, this recall involved a device in Greece that was produced by INEX MEDICAL SA.
What is this?
A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.
Learn more about the data here-
Type of Event
Recall
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Event ID
850469
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Event Date Posted
2014-05-12
- Event Country
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Event Source
NOM
- Event Source URL
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Notes / Alerts
Greek data is current through July 2018. All of the data comes from the National Organization for Medicines, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Greece. -
Extra notes in the data
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Action
Batch recall 20130904-04 of test gloves TITI GLOVE
Device
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Model / Serial
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Product Description
Withdrawal of batch 20130904-04, (dated: 09-2018) of the medical device "TITI GLOVE, Latex Examination Gloves, Size: Large"
- Manufacturer
Manufacturer
- Manufacturer Parent Company (2017)
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Source
NOM