Reported Jul 31, 2019 · Terminated
MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron…
Zevex Incorporated (dba MOOG 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 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 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, 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
Lot numbers CF1819415CF1820215CF1821616CF1822914and CF1823615UDI 38148440000464
- Amount recalled
- 569/20-set caess
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Administration sets leaked at the filter.
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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