FDA Device recall Z-2176-2017
AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only
- FDA Device
- Class II
- terminated
- Published 2017-06-07
On 2017-06-07 the FDA classified a Class II recall of AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only by Abbvie.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2176-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-27 |
| Published | 2017-06-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Abbvie |
| Distribution | US |
Product
AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
Reason
Identifiers
| code_info | Material/List number: 629100116 Lots: 32025245, 32054247, 32265215, 32335206, 32335336 |
|---|
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-2176-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.