Reported Oct 10, 2018 · Terminated
CAPNOSTREAM 20 (US) N, Part Number CS08651
Oridion Medical 1987 Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Oridion Medical 1987 Ltd. · Har Hotzvim Industrial Park Box 45025 · Jerusalem · N/A
Is this the product you have?
CAPNOSTREAM 20 (US) NPart Number CS08651
- Lot codes and dates
2,717 of 2,717 codes
B200001468B200001473B200001476B200001594B200001951B200001980B200001992B200002054B200002129B200002144B200002147B200002149B200002164B200002171B200002204B200002154B200001956B200002085B200002110B200001948B200002048B200002167B200002168B200001953B200001955B200001961B200001964B200001966B200001968B200001969B200001972B200001981B200001991B200002001B200002006B200002008B200002022B200002024B200002033B200002034B200002074B200002075B200002080B200002095B200002111B200002126B200001985B200001717B200001422B200001505B200001599B200001691B200001696B200001783B200001889B200001916B200001919B200001923B200002115B400002214
- Amount recalled
- 3143
This recall covers 37 products
The agency filed one notice per product. You are reading one of them; the other 36 are below.
24 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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