# FDA recall Z-1718-2020

> **Boddingtons Plastics Ltd** · Class II · device recall initiated 2020-03-11.

## 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)

## Distribution

Nationwide  Foreign:

## Key facts

- **Recall number:** Z-1718-2020
- **Recalling firm:** Boddingtons Plastics Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-11
- **Report date:** 2020-04-22
- **Termination date:** 2022-08-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tonbridge, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1718-2020

## Citation

> AI Analytics. FDA recall Z-1718-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1718-2020. Source: US FDA. Licensed CC0.

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