Endocuff Vision: models ARV 110 — Class II medical device recall Z-1718-2020
Terminated recall by Boddingtons Plastics Ltd, reported 2020-04-22, distributed nationwide. Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonosco
| Recall number | Z-1718-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Boddingtons Plastics Ltd, Tonbridge, United Kingdom |
| Recall initiated | 2020-03-11 |
| Classified | 2020-04-16 |
| Reported by FDA | 2020-04-22 |
| Terminated | 2022-08-10 |
| Distributed | Nationwide (US) |
| Quantity | 13,202 units |
| Model numbers | 110, 120, 130, 140 |
Product
Endocuff Vision: models ARV 110, 120, 130, 140 Intended Use: ENDOCUFF VISION is a device attached to the distal end of a colonoscope, designed to maintain and maximize the viewable mucosa during endocosopic therapy by manipulating colonic folds
Reason for recall
Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)
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-1718-2020. 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.