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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85214

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
March 11, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Boddingtons Plastics Ltd

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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

Z-1718-2020
Recall number
Z-1718-2020
Initiated
March 11, 2020
Classification
Class II
Status
Terminated
Recalling firm
Boddingtons Plastics Ltd
Quantity
13202 Units US

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

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Inspect official wording and provenance

Reason for recall

Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)

Code information

All batches distributed prior to 1st May 2020.

Distribution pattern

Nationwide Foreign: