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FDA (Device enforcement)Recalled 2024-04-09class ii

Sophysa S.A.: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit monitoring is intended for monitoring intracranial ventricular pressure and temperature with tunneling (PSO-VTT) ind

Hazard

An increase in claims related to leakage of cerebrospinal fluid (CSF) from the proximal end of the catheter. In the event of a leak going undetected during implantation, it could pose an infectious risk to the patient. The cause of the leaks is indicated to be manufacturing error involving perforation of the inner channel of the catheter during stylet insertion.

Details from the source

Reason for recall: An increase in claims related to leakage of cerebrospinal fluid (CSF) from the proximal end of the catheter. In the event of a leak going undetected during implantation, it could pose an infectious risk to the patient. The cause of the leaks is indicated to be manufacturing error involving perforation of the inner channel of the catheter during stylet insertion. Distribution: Worldwide - US Nationwide distribution in the states of AZ, NY, TX and the countries of ARGENTINA, CHINA, CZECH REPUBLIC, FRANCE, GREECE, HUNGARY, JAPAN, PAKISTAN, Portugal, ROMANIA, SOUTH AFRICA, SWEDEN, VIETNAM. Quantity: 3175 units- 41 units US; 3134 units OUS Lot/code info: UDI-DI: 3760124132922 US Serial Numbers: 22D06059 22D06060 22D06745 22D06747 22D06749 22D07240 22D07242 22D07243 22D07246 22D07249 22D07250 22D07251 22D07257 22D08435 22D08436 22D08438 22D08511 22D08512 22D08522 22D08525 22D08526 22D08527 22D08528 22D08529 22D12007 22D12009 22D12012 22D12013 22D12014 22D12016 22D12017 22D12018 22D12019 22D12020 22D12021 22D12022 22D12023 22D12024 22D12025 22D12027 22D12032 OUS S/N: 22D04871 22D04873 22D04875 22D04877 22D04881 22D04907 22D04908 22D04909 22D05006 22D05021 22D09368 22D09376 22D09377 22D09378 22D09379 22D09380 22D09381 22D09382 22D09383 22D09384 22D52761 22D52764 21D20346 21D20353 21D20355 21D20361 21D20367 21D42206 21D42212 21D42215 21D42240 22D00060 22D00064 22D00065 22D00066 22D00067 22D00068 22D00069 22D00070 22D00071 22D00072 22D00074 22D00075 22D00076 22D00077 22D00084 22D00124 22D00240 22D00241 22D00242 22D00244 22D00245 22D00247 22D00248 22D00253 22D00256 22D00258 22D00259 22D00262 22D00263 22D00264 22D00265 22D00267 22D00269 22D00271 22D00276 22D00277 22D00278 22D00279 22D00286 22D00290 22D00292 22D00297 22D00298 22D00299 22D00301 22D00302 22D00304 22D00307 22D00310 22D00313 22D00315 22D00616 22D00621 22D00622 22D00636 22D00637 22D00638 22D00640 22D00643 22D00645 22D00649 22D00650 22D00661 22D00665 22D00666 22D00667 22D00668 22D00670 22D00671 22D00672 22D00673 22D00674 22D00675 22D00676 22D00677 22D00678 22D00679 22D00680 22D00681 22D00682 22D00683 22D00684 22D00685 22D00686 22D00687 22D00690 22D00691 22D00692 22D00736 2

UPC codes

3760124132922

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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