FDA Device recall Z-1649-2016
Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 584400 (OUS) Intended to provide enteral nutrition to a patient for hospital an…
- FDA Device
- Class II
- terminated
- Published 2016-05-18
On 2016-05-18 the FDA classified a Class II recall of Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 584400 (OUS) Intended to provide enteral nutrition to a patient for hospital an… by Medtronic, citing kangaroo Connect Feeding Pump Occlusion alarms fail to alarm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1649-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-04-01 |
| Published | 2016-05-18 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic |
| Distribution | n/a |
Product
Covidien Kangaroo Connect Enteral Feeding Pump Item Number: 584400 (OUS) Intended to provide enteral nutrition to a patient for hospital and acute care settings.
Reason
Kangaroo Connect Feeding Pump Occlusion alarms fail to alarm
Identifiers
| code_info | Serial Numbers: AS1400000006 AS1400000007 AS1400000008 AS1400000010 AS1400000011 AS1400000012 AS1400000013 AS14…Serial Numbers: AS1400000006 AS1400000007 AS1400000008 AS1400000010 AS1400000011 AS1400000012 AS1400000013 AS1400000014 AS1400000015 AS1400000016 AS1400000017 AS1400000020 AS1400000022 AS1400000023 AS1400000024 AS1400000025 AS1400000026 AS1400000027 AS1400000028 AS1400000029 AS1400000031 AS1400000032 AS1400000033 AS1400000034 AS1400000035 AS1400000036 AS1400000037 AS1400000038 AS1400000039 AS1400000040 AS1400000041 AS1400000042 AS1400000043 AS1400000045 AS1400000046 AS1400000047 AS1400000049 AS1400000050 AS1400000051 AS1400000052 AS1400000054 AS1400000055 AS1400000057 AS1400000058 AS1400000059 AS1400000060 AS1400000061 AS1400000062 AS1400000063 AS1400000064 AS1400000065 AS1400000066 AS1400000067 AS1400000068 AS1400000069 AS1400000070 AS1400000072 AS1400000077 AS1400000078 AS1400000079 AS1400000080 AS1400000081 AS1400000082 AS1400000083 AS1400000089 AS1400000091 AS1400000092 AS1400000101 AS1400000103 AS1400000104 AS1 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1649-2016%22
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