Health product recall

Endocuff Vision (2020-04-16)

Starting date:
April 16, 2020
Posting date:
May 8, 2020
Type of communication:
Medical Device Recall
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Medical Devices
General Public, Healthcare Professionals, Hospitals
Identification number:

Last updated: 2020-05-08

Affected Products

Endocuff Vision


Boddingtons, the manufacturer is notifying customers regarding the update to an IFU for Endocuff Vision model numbers ARV110, ARV120, ARV130, and ARV140. The new IFU will include the following information relating to contraindications and potential complications/adverse events of the colonoscopy procedure.

Contraindication: the Endocuff Vision should not be used in cases with acute, severe colitis, diverticulitis or where there is known colonic stricture.

Potential complication or adverse events: no common adverse events or complications for Endocuff Vision are known. However,

potential complications related to colonoscopy include, but are not limited to perforation, bleeding, infection, discomfort and allergic reaction to sedation agents.

Boddingtons has determined that customers may continue to use products on hand provided users are aware of the updated information. The updated IFU will accompany new products starting in May 2020.


Affected products

Endocuff Vision

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number
  • ARV 110
  • ARV 120
  • ARV 130
  • ARV 140


Unit 6, Whellbarrow Park Estate, Pattenden Lane

Tonbridge, Kent

TN12 9QJ