MOOG Medical Devices Group
MOOG Medical Devices Group appears in FDA public data with 5 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0688-2016, Class II) was initiated on December 23, 2015.
Summary
- Total Recalls
- 5
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0688-2016 | Class II | Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curl | December 23, 2015 |
| Z-0415-2016 | Class II | Catalog No. INF0020-A EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System an | November 20, 2015 |
| Z-0294-2013 | Class II | EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INF | November 8, 2012 |
| Z-0764-2013 | Class II | Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual | October 12, 2012 |
| Z-0072-2013 | Class II | ***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Admin | September 26, 2012 |