AbbVie PEG Kit 20 FR — Class II medical device recall Z-0786-2017
Terminated recall by AbbVie Inc., reported 2016-12-28, distributed in PR. AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnecti
| Recall number | Z-0786-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AbbVie Inc., North Chicago, IL, United States |
| Recall initiated | 2016-11-22 |
| Classified | 2016-12-17 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2019-07-09 |
| Distributed | PR |
| Quantity | 541 units |
| Lot numbers | 32025245, 32265215, 32335206, 32335336 |
Product
AbbVie PEG Kit 20 FR
Reason for recall
AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0786-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.