Lower riskMedical device recall · FDA · Published January 18, 2018
Angiodynamics Fluid Management Kits: Minor Procedure Delay Hazard
Angiodynamics recalls fluid management kits with specific lot numbers due to assembly issues causing minor procedure delays. Affected kits may not function properly during medical procedures.
NAMIC Fluid Management Convenience Kits contains a Fluid Delivery Set that was not assembled in accordance with specification, and prevents the device from being used, resulting in a minor delay in procedure.
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Contact the company
📍Recalling firmAngiodynamics Inc. (Navilyst Medical Inc.)10 Glens Falls Tech Park · Glens Falls, NY 12801-3864
✎ GovInfoNow plain-language explainer
Angi:odynamics recalls certain fluid management kits used in medical procedures because they were not assembled correctly, which can cause minor delays during surgery. This does not pose a serious safety risk but requires immediate attention to avoid procedure delays. Read more at govinfonow.com/recall/72125-angiodynamics-fluid-management-kits-minor-procedure-delay-hazard.
“Angiodynamics Fluid Management Kits: Minor Procedure Delay Hazard.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72125-angiodynamics-fluid-management-kits-minor-procedure-delay-hazard. Based on FDA recall #Z-1390-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1390-2018%22&limit=1).
The FDA announced on Jan. 18, 2018, that Angiodynamics Inc. (Navilyst Medical Inc.) recalled Fluid Management Convenience Kits due to assembly errors preventing device use. The recall affects 38 units distributed to end users.
Lot Numbers: 5284422, 5286610, 5283649, 5290525, 5286542
Quantity: 38 units
The hazard
The NAMIC Fluid Management Convenience Kits contain a Fluid Delivery Set not assembled in accordance with specifications. This defect prevents the device from being used, resulting in a minor delay in procedure.
Context
GovInfoNow's records show Angiodynamics Inc. (Navilyst Medical Inc.) has had 8 other recalls since Oct. 17, 2017. Other recent recalls of similar products include Angiodynamics Smart Port CT-Implantable Port Recall (Feb. 22, 2021), Starburst Talon Electrosurgical Device Recalled for Incorrect Labeling (Oct. 2, 2019), and Angiodynamics BIOFLO 8F Device May Delay Implantation Due to Connector Issue (Sept. 18, 2019). Other recent recalls of similar products include Medline Medical Kits Recall: Particulate Risk in Fluid Path (March 24, 2026), Medline Medical Kits Recall: Particulate in Fluid Path Risk (March 24, 2026), and Medline Neuro Angio Pack Kits Recall (Nov. 26, 2025).
How to tell if you have this one
Check the lot numbers on the kit: 5284422, 5286610, 5283649, 5290525, or 5286542. These kits were sold for use in fluid management and invasive pressure monitoring systems.
Brand
Angiodynamics
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Kit Lot Numbers
Identify the lot numbers on the kit: 5284422, 5286610, 5283649, 5290525, or 5286542.
How this recall unfolded
Recall timeline
FDA terminated this recall 8 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1390-2018 (January 18, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1390-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.