PlainRecalls

Oridion Medical 1987 Ltd.

47 recalls on record · Latest: Mar 26, 2025

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Agency notice ledger

Federal filing book Oridion Medical 1987 Ltd. MID-BOOK · SINGLE-AGENCY

#380 of 14,151 · 47 notices · 0.045% archive

  • BOOK 47 notices
  • RANK #380 of 14,151
  • SHARE 0.045% archive
  • AGENCY FDA Devices (47)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 26, 2025
  • PHOTO Arrow International,…

Nearest notice-volume peer: Arrow International, LLC (0 notice gap)

Oridion Medical 1987 Ltd. accounts for about 0.045% of the 104,423-notice archive on 47 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Oridion Medical 1987 Ltd. sits among 14,151 recalling firms

Oridion Medical 1987 Ltd. ranks 380th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Oridion Medical 1987 Ltd. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

47 380th of 14151 higher than 13,768 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14

Oridion Medical 1987 Ltd. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Oridion Medical 1987 Ltd. holds about 0.045% of archive notices alongside 47 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Filter Line Sets Adult/Pediatric & Infant/Neonatal, 10129497 - CapnoLine Neonatal-Infant Intubated Filter Line with Microstream Technology H, Length 7 (2.0 m), 006324COV; CapnoLine Adult-Pediatric Intubated Filter Line with Microstream Technology Length 7 (2.0 m), XS04620COV; CapnoLine Adult-Pediatric Intubated Filter Line with Microstream Technology H, Length 7 (2.0 m), XS04624COV

FDA Devices Moderate Mar 26, 2025

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

FDA Devices Moderate Mar 26, 2025

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-

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Airway Adapter and CO2 Sampling Line, 01158 - Microstream Luer Adult-Pediatric Airway Adapter, 010989; Omnistream CO2 Sampling Line X25, 010991

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Advance Intubated Adult-Pediatric, PT00156254 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Short-term use: Procedural/Emergency, MVAI; Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Short-term use: Procedural/Emergency, MVAI100U; Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Extended Duration, MVAIH; Micr

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: OmniVentLine Set, 012808 - OmniVentLine Set Adult-Pediatric CO2 Sampling Line and Airway Adapter, 012495;

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Luer Intubated Adult Pediatric, PT00156355 - Microstream Luer Adult-Pediatric Intubated CO2 Sampling Line 2m/6.5ft Short-term use: Procedural/Emergency, MLAI

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration, QMVIIH

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Adult-Pediatric Intubated, PT00134333 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Short-term use: Procedural/Emergency, QMVAI; Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Extended Duration, QMVAIH

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H Set Infant/Neonatal, 006147 - MICROSTREAM FilterLine H Set Infant/Neonatal CO2 Sampling Line and Airway Adapter for Humid Environments, 006324; MICROSTREAM FilterLine H Set Long Infant/Neonatal CO2 Sampling Line and Airway Adapter for Humid Environments, 007738; MICROSTREAM VitaLine H Set Infant/Neonatal CO2 Sampling Line and Airway Adapter for Humid Environments, 01080

FDA Devices Moderate Oct 10, 2018

Capnostream20 M ADULT ICU (CPM), CS08654RA

FDA Devices Moderate Oct 10, 2018

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

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N W/PRINTER, Part Number CS08657-01

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) N W/PRINTER REFURBISHED, Part Number CS78657

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20 (INTL) N W/PRINTER, Part Number CS08658

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) M, CS08654

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) N REFURBISHED, CS78652

FDA Devices Moderate Oct 10, 2018

Capnostream20 M NICU (CPM), CS08654RN

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-03

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20 (INTL) N, Part Number CS08652

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N W/PRINTER, Part Number CS08658-01

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) M, Part Number CS08653

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20 (US) N W/PRINTER, Part Number CS08657

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS, CS051COV-03

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) M W/PRINTER REFURBISHED, CS78660

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) M W/PRINTER REFURBISHED, Part Number CS78659

FDA Devices Moderate Oct 10, 2018

Capnostream20 N CYVITAL, CS08799

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N, Part Number CS08652-01

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US)M REFURBISHED, Part Number CS78653

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) M TO MASIMO, Part Number CS08750

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) M REFURBISHED, CS78654

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) N W/PRINTER REFURBISHED, CS78658

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) M W/PRINTER TO MASIMO, Part Number CS08751

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-03

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS, CS08658-02

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N W/PRINTER - ROHS, Part Number CS08657-02

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) N REFURBISHED, Part Number CS78651

FDA Devices Moderate Oct 10, 2018

Capnostream20 N W/PRINTER CYVITAL, CS08798

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N, Part Number CS08651-01

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (COV-INTL) N W/PRINTER ROHS, CS051COV

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-02

FDA Devices Moderate Oct 10, 2018

Capnostream20 M W/PRINTER CYVITAL, CS08796

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) M W/PRINTER, CS08660

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) M W/PRINTER, Part Number CS08659

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20 (US) N, Part Number CS08651

Oridion Medical 1987 Ltd. holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (47 here — heavy-book).

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Frequently Asked Questions

How many federal recall notices name Oridion Medical 1987 Ltd.?
PlainRecalls indexes 47 distinct federal recall events naming Oridion Medical 1987 Ltd., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Oridion Medical 1987 Ltd. sit among other recalling firms?
Oridion Medical 1987 Ltd. ranks #380 of 14,151 by distinct recall-event count among 14,151 firms in this archive (97th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Oridion Medical 1987 Ltd.'s notices?
FDA Devices accounts for 47 of this firm's 47 indexed notices.
What product category dominates Oridion Medical 1987 Ltd.'s filing book?
Filings for Oridion Medical 1987 Ltd. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Oridion Medical 1987 Ltd.: 47 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Oridion Medical 1987 Ltd.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026