Atlas FDA

Oridion CO2 sampling lines and water traps under the label: MicroStreamC02 Sampling Lines: FilterLine Set Adult/Pediatri

FDA device recall Z-1332-2012 · posted 2012-03-29 · Terminated

Recall details

Recalling firm
Oridion Medical 1987 Ltd.
Reason for recall
CO2 sampling lines may have paper and plastic particulate present in the packaged units at levels that may exceed visual specification.
Action taken
Oridion notified Hospitals, Clinics, EMS with an "Important Communication" letter to clinicians dated February 12, 2012. The letter was intended to make US clinicians aware of an important issue relating to certain Oridion CO2 sampling lines, which may not fully meet quality requirements. In a few cases, paper and plastic particulate may be present in the packaged units at levels that exceed the visual specification. Recommended actions were included in the letter. Questions were directed to 1(781)-972-1252.
Root cause
Packaging process control
Status
Terminated
Product code
CCK
Quantity affected
2 million
Distribution
Nationwide Distribution
Date initiated
2012-02-16
Date posted
2012-03-29
Date terminated
2013-09-13
Location
Jerusalem, Har Hotzvim Industrial Park, Israel

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Related 510(k) clearances

RecordFirmDate
MICROSTREAM O2/CO2 ORAL NASAL FILTERLINE (K011536)Oridion Medical 1987 , Ltd.2001-11-14
MICROSTREAM ORAL NASAL CANNULA FILTERLINE (K011050)Oridion Medical 1987 , Ltd.2001-05-04
O2/CO2 NASAL FILTERLINE (K010024)Oridion Medical 1987 , Ltd.2001-03-14
MICROSTREAM FILLERLINE OR/EMS (K980324)Oridion Medical , Ltd.1998-04-16
MICROSTREAM NASAL CANNULA FILTERLINE (K980325)Oridion Medical , Ltd.1998-04-16
MICROSTREAM FILTERLINE ICU (K980327)Oridion Medical , Ltd.1998-04-16