Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported May 23, 2018
Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24 lines per case. The Nipro¿ Set - Blood Tubing Set with Transducer Protector and Priming Set are disposable bloodlines intended to provide extracorporeal access to the patient s blood during hemodialysis. The compatibility of available configurations is the responsibility of the physician in charge.
There is a possibility of the heparin line is occluded.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Nipro Medical Corporation recalled Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packag… - a moderate-severity action.
Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packag… was recalled by Nipro Medical Corporation in May 23, 2018. Reason: There is a possibility of the heparin line is occluded.. Check the official notice for the remedy. Verify recall #Z-1876-2018 with the FDA Devices before acting.
The recall
Nipro Medical Corporation issued this moderate-severity FDA Devices recall-There is a possibility of the heparin line is occluded..
- Moderate
- severity level
- 308K units
- affected scope
- Class II
- classification
- May 23, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1876-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1876-2018) was formally reported on May 23, 2018, with the manufacturer initiating the action on December 19, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Nipro Medical Corporation is listed as the recalling firm, operating out of Doral, FL. Federal records list the affected scope as 307,944 units., a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: There is a possibility of the heparin line is occluded. Distribution data in the federal record shows the product reached: US Distribution to the states of : GA, NY, TN, TX.. 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
307,944 units.
Related Recalls
6
3 from same agency
Product description
Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24 lines per case. The Nipro¿ Set - Blood Tubing Set with Transducer Protector and Priming Set are disposable bloodlines intended to provide extracorporeal access to the patient s blood during hemodialysis. The compatibility of available configurations is the responsibility of the physician in charge.
Reason for recall
There is a possibility of the heparin line is occluded.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1876-2018 |
| Date reported | May 23, 2018 |
| Date initiated | December 19, 2017 |
| Recalling firm | Nipro Medical Corporation |
| Firm location | Doral, FL |
| Affected scope | 307,944 units. |
| Distribution | US Distribution to the states of : GA, NY, TN, TX. |
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-1876-2018) 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? ▼
Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24 lines per case. The Nipro¿ Set - Blood Tubing Set with Transducer Protector and Priming Set are disposable bloodlines intended to provide extracorporeal access to the patient s blood during hemodialysis. The compatibility of available configurations is the responsibility of the physician in charge.. Recalled by Nipro Medical Corporation. Units affected: 307,944 units..
Why was this product recalled? ▼
There is a possibility of the heparin line is occluded.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 23, 2018. Severity: Moderate. Recall number: Z-1876-2018.
Where was the recalled product distributed? ▼
Distribution: US Distribution to the states of : GA, NY, TN, TX..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1876-2018) 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 May 23, 2018. 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.