Reported Mar 7, 2018 · Terminated
MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged…
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 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, 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 38148440000396
- Lot/serial numbers
74 of 74 codes
CF1514703CF1514702CF1514702CF1514701CF1514702CF1517405CF1517406CF1518301CF1518302CF1518303CF1518301CF1521101CF1521103CF1521102CF1521701CF1522306CF1522308CF1522307CF1523312CF1524407CF1524407CF1525101CF1524407CF1525103CF1525102CF1526505CF1526506CF1527307CF1527306CF1528011CF1528607CF1528606CF1529306CF1529307CF1530106CF1530707CF1530706CF1530706CF1530705CF1530706CF1530707CF1530706CF1530707CF1532102CF1531406CF1532102CF1531405CF1532975CF1532976CF1532976CF1532976CF1532976CF1535001CF1533504CF1534902CF1535666CF1600507CF1600508CF1601203CF1601903
- Amount recalled
- 56,244/20 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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