Curlin Administration Set recallZ-2054-2019 · Zevex Incorporated (dba MOOG Medical Devices Group) · initiated Feb 27, 2019
Terminated
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Zevex Incorporated (dba MOOG Medical Devices Group) or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Administration sets leaked at the filter.
FDA root cause category: Nonconforming Material/Component
What the company is doing
The recalling firm issued a letter dated 2/27/2019 via regular mail on 2/272019 to their direct accounts describing the issue, risk to health, and the necessary actions to be taken.
Recall details
- Recall number
- Z-2054-2019
- Status
- Terminated
- Initiated by the company
- Feb 27, 2019
- Posted by the FDA
- Jul 23, 2019
- Recalling firm
- Zevex Incorporated (dba MOOG Medical Devices Group)
- Quantity
- 756/20-set cases
- Product code
- FRN
- FDA submissions
- K981816
- Distribution
- Distribution was made to GA, IL, KS, MA, MI, and OH. There was no foreign/military/government distribution.
Product description
MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.
Code information (models, lots, serial numbers)
Lot numbers CF1820216, CF1821617, CF1822214, and CF1823616, UDI 38148440000471.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Curlin Administration Set 340-4130-VZevex International, Inc. · Pump, Infusion1 recall0 reports
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 82864).
- Z-2053-2019 · TerminatedMOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile. Product Usage: Ad…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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