🔍 RecallPedia

CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS, CS08658-03

Class I - Dangerous
🏥 Medical Devices Recalled: July 31, 2018 Oridion Medical 1987 Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    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 PA24172446 PA24172447 PA24172448 PA24172449 PA24172450 PA24172451 PA24172452 PA24172453 PA24172454 PA24172455 PA24172472
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Oridion Medical 1987 Ltd.
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS, CS08658-03

Product Codes/Lot Numbers:

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 PA24172446 PA24172447 PA24172448 PA24172449 PA24172450 PA24172451 PA24172452 PA24172453 PA24172454 PA24172455 PA24172472

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0043-2019

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Oridion Medical 1987

Class I - Dangerous

Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect adapter from endotracheal tube for procedures (e.g. suctioning), may cause treatment delay and/or unintended extubation, which could lead to respiratory failure, hypoxia, aspiration, and/or low oxygen saturation.

Feb 17, 2025 Other Medical Devices Nationwide View Details →

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Advance Intubated Infant, PT00156250 - Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration, MVIIH; Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft High Humidity, MVIIHH; Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 4m/13ft Extended Duration, MVIIHL; Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration, ZMVIIH

Oridion Medical 1987

Class I - Dangerous

Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect adapter from endotracheal tube for procedures (e.g. suctioning), may cause treatment delay and/or unintended extubation, which could lead to respiratory failure, hypoxia, aspiration, and/or low oxygen saturation.

Feb 17, 2025 Other Medical Devices Nationwide View Details →

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine Sets & VitaLine Sets Adult/Pediatric, MQ04616 - MICROSTREAM FilterLine H Set Long Adult-Pediatric CO2 Sampling Line and Airway Adapter for Humid Environments, 007737; MICROSTREAM FilterLine Set Long Adult-Pediatric CO2 Sampling Line and Airway Adapter, 007768; MICROSTREAM FilterLine Set Adult-Pediatric CO2 Sampling Line and Airway Adapter, 010579; MICROSTREAM FilterLine H Set Adult-Pediatric CO2 Sampling Line and Airway Adapter for Humid Environments, 010580; MICROSTREAM VitaLine H Set Adult-Pediatric CO2 Sampling Line and Airway Adapter for High Ambient Humidity X25, 010787; MICROSTREAM FilterLine Set Adult-Pediatric CO2 Sampling Line and Airway Adapter for Humid Environments, 015016; MICROSTREAM FilterLine Set Adult-Pediatric CO2 Sampling Line and Airway Adapter, 015021; MICROSTREAM FilterLine Set Adult-Pediatric CO2 Sampling Line and Airway Adapter, XS04620; MICROSTREAM FilterLine H Set Adult-Pediatric CO2 Sampling Line and Airway Adapter for Humid Environments, XS04624.

Oridion Medical 1987

Class I - Dangerous

Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect adapter from endotracheal tube for procedures (e.g. suctioning), may cause treatment delay and/or unintended extubation, which could lead to respiratory failure, hypoxia, aspiration, and/or low oxygen saturation.

Feb 17, 2025 Other Medical Devices Nationwide View Details →