PlainRecalls

Oridion Medical 1987 Ltd.

30 recalls on record · Latest: Mar 26, 2025

Oridion Medical 1987 Ltd. Recall Insight

Oridion Medical 1987 Ltd. appears on 30 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.036% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Mar 26, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 30 entries, severity tagging shows 0 critical, 30 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 30 of 30 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (30). The date window on this page runs from Oct 10, 2018 to Mar 26, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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, 101294…

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Advance Intubated Infant, PT00156250 - Mic…

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 -…

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 - Microstr…

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Advance Intubated Adult-Pediatric, PT00156254 …

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: OmniVentLine Set, 012808 - OmniVentLine Set Adult-Pedi…

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Luer Intubated Adult Pediatric, PT00156355 - …

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Micros…

FDA Devices Moderate Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Adult-Pediatric Intubated, PT00134333 - …

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

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds