Oridion CO2 sampling lines and water traps under the label: Surestream CO2 Sampling Lines: SureLine Adult Part No.010976; sureLine Pediatric Part No. 010977; SureLine O2 Adult Part No.010979; SureLine O2 Pediatric Part No.010980 Smart SureLine Plus O2 Adult Part No. 010981; Smart SureLine O2 Pediatric Part No. 010982; Smart SureBloc O2 Part No. 010983; Watertrap (package of 25 units) Part No. 010994; Sure VentLine Set Adult/Pediatric Part No.010986; Sure VentLine H Set Adult/Pediatric Part No.010987; Smart SureLine Guardian O2 Part No.012533; Smart SureLine Guardian O2 Long Part No.012534;
FDA Recall Z-1333-2012 · Posted 2012-03-29
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Recalling FirmOridion Medical 1987 Ltd.
Recall StatusTerminated
Product CodeCCK
Date Initiated2012-02-16
Date Terminated2013-09-13
Product Quantity2 million
Reason for Recall
CO2 sampling lines may have paper and plastic particulate present in the packaged units at levels that may exceed visual specification.
Firm Action
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
Distribution Pattern
Nationwide Distribution
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
K042665SMART BITEBLOCOridion Medical 1987 , Ltd. · 2004-11-23K013845MODIFICATION TO: MAC-LINE O2/CO2 ORAL NASAL CANNULA SAMPLE LINEOridion Medical 1987 , Ltd. · 2001-11-29K012391MAC-LINE CO2 NASAL CANNULA SAMPLE LINEOridion Medical 1987 , Ltd. · 2001-08-15K012395MAC-LINE 02/CO2 NASAL CANNULA SAMPLE LINEOridion Medical 1987 , Ltd. · 2001-08-15K980324MICROSTREAM FILLERLINE OR/EMSOridion Medical , Ltd. · 1998-04-16K980327MICROSTREAM FILTERLINE ICUOridion Medical , Ltd. · 1998-04-16
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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