Reported Mar 7, 2018 · Terminated
MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site…
Zevex Incorporated (dba Moog Medical Medical Devices Group)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Zevex Incorporated (dba Moog Medical Medical Devices Group) · 4314 S Zevex Park Ln · Salt Lake City, UT · 84123-7881
Is this the product you have?
- MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site with Check Valve, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile
- Product UsageAdministration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions
- Lot codes and dates
- UDI 38148440000495
- Lot/serial numbers
CF1518304CF1521104CF1524301CF1523803CF1528603and CF1613101
- Amount recalled
- 2,497/20-administration set cases
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
Particulate found on the Curlin spike.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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