Recall Z-1648-2016— Medtronic
Class II · Terminated
Class II FDA medical device recall by Medtronic, initiated 2016-04-01, terminated 2018-05-18. It names one FDA 510(k) clearance: K143263. Product: Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 384400 (US) Intended to provide enteral nutrition to a patient for hospital and acute care settings.. Reason: Kangaroo Connect Feeding Pump Occlusion alarms fail to alarm.
- Recalling firm
- Medtronic
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-04-01
- Terminated
- 2018-05-18
- Firm location
- North Haven, CT, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
Product description
Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 384400 (US) Intended to provide enteral nutrition to a patient for hospital and acute care settings.
Reason for recall
Kangaroo Connect Feeding Pump Occlusion alarms fail to alarm
Data sourced from openFDA. This site is unofficial and independent of the FDA.