Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported April 12, 2023
CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE
Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where t…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Terumo Cardiovascular Systems Corporation recalled CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE - a moderate-severity action.
CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE was recalled by Terumo Cardiovascular Systems Corporation in April 12, 2023. Reason: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded …. Check the official notice for the remedy. Verify recall #Z-1346-2023 with the FDA Devices before acting.
The recall
Terumo Cardiovascular Systems Corporation issued this moderate-severity FDA Devices recall-Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded ….
- Moderate
- severity level
- 84 units
- affected scope
- Class II
- classification
- April 12, 2023
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1346-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1346-2023) was formally reported on April 12, 2023, with the manufacturer initiating the action on March 1, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Terumo Cardiovascular Systems Corporation is listed as the recalling firm, operating out of Elkton, MD. Federal records list the affected scope as 84 units.
The documented reason for this recall is: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bon… Distribution data in the federal record shows the product reached: US Nationwide. Belgium, Canada, Costa Rica, Thailand.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
84 units
Related Recalls
6
3 from same agency
Product description
CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE
Reason for recall
Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1346-2023 |
| Date reported | April 12, 2023 |
| Date initiated | March 1, 2023 |
| Recalling firm | Terumo Cardiovascular Systems Corporation |
| Firm location | Elkton, MD |
| Affected scope | 84 units |
| Distribution | US Nationwide. Belgium, Canada, Costa Rica, Thailand. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1346-2023) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE. Recalled by Terumo Cardiovascular Systems Corporation. Units affected: 84 units.
Why was this product recalled? ▼
Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 12, 2023. Severity: Moderate. Recall number: Z-1346-2023.
Where was the recalled product distributed? ▼
Distribution: US Nationwide. Belgium, Canada, Costa Rica, Thailand..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1346-2023) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported April 12, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.