Devices

Device Recall StayFix

Model / Serial
Lot numbers: 551268, 551537, 551615, 551616, 551702, 551703, 551704, 553104, 553360, 553361, 553362, 553363, 554362, 554367, 554368, 554483, 554497, 554504, 554505, 554506, 554723, 554764, 554765, 554766, 555638, 555639, 555655, 555656, 555657, 555658, 556406, 556407, 556408, 556409, 556410, 556411, 556842, 556843, 556844, 556845, 556846, 556847, 556871, 556872, 556873, 556874, 556875, 562518, 562748, 562874, 563254, 563255, 563388, 563389, 566538, 566899, 566900, 566901, 566902, 566903, 566904, 567248, 567515, 567596, 567599, 567600, 567601, 567767, 567835.
Product Classification
General Hospital and Personal Use Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide, including USA, France, Germany, and United Kingdom.
Product Description
StayFix Fixation Device for Percutaneous catheters, REF 680ME, (small) 5F - 14F, Merit Medical, Unomedical, Ltd., Great Britain.
Manufacturer
Merit Medical Systems, Inc
1 Event
- Recall of Device Recall StayFix

Manufacturer

Merit Medical Systems, Inc

Manufacturer Address
Merit Medical Systems, Inc, 1600 West Merit Pkwy, South Jordan UT 84095-2416
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall StayFix

Model / Serial
Lot Numbers: 547745, 551172, 554699, 555705, 555706, 556394, 556395, 556396, 556876, 556877, 558988, 560767, 560768, 560781, 561127, 561144, 562749, 562750, 563256, 563257, 563387, 564684, 564685, 565284, 565285, 565353, 565955, 566684, 566905, 566906, 566907, 567383, 567513, 567728, 569474.
Product Classification
General Hospital and Personal Use Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide, including USA, France, Germany, and United Kingdom.
Product Description
StayFix Fixation Device for Percutaneous catheters, REF 685ME, (large) 12F - 22F, Merit Medical, Unomedical, Ltd., Great Britain.
Manufacturer
Merit Medical Systems, Inc

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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