CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS, CS08658-03
Medical device recall Z-0043-2019. Published in FDA’s Enforcement Report on Oct 10, 2018.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Oct 10, 2018. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 1 state named
- 192 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS, CS08658-03
192, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
PA14170895 PA14170897 PA14170903 PA14170930 PA14170937 PA14170944 PA14170952 PA14170954 PA14170956 PA14170961 PA14170962 PA14170963 PA14170964 PA14170965 PA14170966 PA14170967 PA14170968 PA14170969 PA14170970 PA14170971 PA14170973…
Every code shown here, 1,991 characters
PA14170895 PA14170897 PA14170903 PA14170930 PA14170937 PA14170944 PA14170952 PA14170954 PA14170956 PA14170961 PA14170962 PA14170963 PA14170964 PA14170965 PA14170966 PA14170967 PA14170968 PA14170969 PA14170970 PA14170971 PA14170973 PA14170974 PA14170975 PA14170976 PA14170977 PA14170978 PA14170979 PA14170980 PA14170981 PA14170982 PA14170983 PA14170984 PA14170985 PA14170986 PA14170987 PA14170988 PA14170989 PA14170990 PA14170991 PA14170992 PA14170993 PA14170994 PA14170995 PA14170996 PA14170997 PA14170998 PA14170999 PA14171000 PA15171001 PA15171002 PA15171003 PA15171004 PA15171005 PA15171006 PA15171007 PA15171008 PA15171009 PA15171010 PA15171011 PA15171012 PA15171013 PA15171014 PA15171015 PA15171016 PA15171017 PA15171018 PA15171019 PA15171020 PA15171021 PA15171022 PA15171023 PA15171024 PA15171025 PA15171026 PA15171027 PA15171028 PA15171029 PA15171030 PA15171031 PA15171032 PA15171033 PA15171034 PA15171035 PA15171036 PA15171037 PA15171038 PA15171039 PA15171040 PA15171041 PA15171042 PA15171043 PA15171044 PA15171045 PA15171046 PA15171047 PA15171048 PA22172187 PA23172256 PA23172257 PA23172258 PA23172259 PA23172260 PA23172261 PA23172262 PA23172263 PA23172264 PA23172265 PA23172266 PA23172267 PA23172268 PA23172269 PA23172270 PA23172271 PA23172272 PA23172273 PA23172274 PA23172275 PA23172276 PA23172277 PA23172278 PA23172279 PA23172280 PA23172281 PA23172282 PA23172283 PA23172284 PA23172285 PA23172286 PA23172287 PA23172288 PA23172289 PA23172290 PA23172291 PA23172292 PA23172294 PA23172295 PA23172296 PA23172297 PA23172298 PA23172299 PA23172301 PA23172398 PA23172399 PA23172400 PA24172401 PA24172402 PA24172404 PA24172405 PA24172406 PA24172407 PA24172409 PA24172410 PA24172412 PA24172414 PA24172416 PA24172417 PA24172418 PA24172419 PA24172420 PA24172421 PA24172422 PA24172423 PA24172424 PA24172425 PA24172426 PA24172427 PA24172428 PA24172429 PA24172430 PA24172431 PA24172432 PA24172433 PA24172435 PA24172436 PA24172437 PA24172438 PA24172439 PA24172440 PA24172443 PA24172444 PA24172445…
FDA’s list runs to 2,111 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
The products were distributed US nationwide and Puerto Rico. The products were distributed to the following foreign countries: Argentina, Australia, Austria, Bahrain, Belgium, Canada, Columbia, Costa Rica, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Hungary, Ireland, Israel, Italy, Japan, Kazakhstan, Kuwait, Mexico, Netherlands, Norway, Oman, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, Tunisia, Turkey, UAE, UK, and Vietnam.
The states and territories these words name
- Puerto Rico
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jul 31, 2018.
- FDA classified it on Oct 3, 2018.
- FDA’s Enforcement Report published it on Oct 10, 2018.
- FDA terminated it on Sep 20, 2022.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Oridion Medical 1987 Ltd., of Jerusalem, Israel.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 2,111 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.