Boddingtons Plastics recalls Endocuff Vision models ARV 110, 120, 130, 140 due to updated use instructions that may lead to complications during colonoscopy procedures.
Updated Instructions For Use- to contraindications and potential complications/adverse events of the colonoscopy procedure (without using Endocuff Vision Device)
Boddingtons Plastics is recalling Endocuff Vision models ARV 110, 120, 130, and 140 because their updated instructions for use could cause complications during colonoscopy procedures. This affects devices used by medical professionals for colonoscopies.
The updated instructions for use may lead to complications during colonoscopy procedures if the Endocuff Vision device is not used correctly. This device is designed to maintain and maximize the viewable mucosa during endoscopic procedures by manipulating colonic folds.
Medical professionals who use Endocuff Vision devices for colonoscopies are most at risk. The recall applies to all units distributed before May 1, 2020.
Check for Endocuff Vision models ARV 110, 120, 130, or 140. The devices were distributed before May 1, 2020, and are used with colonoscopes for endoscopic procedures.
Identify the model number on your Endocuff Vision device to confirm it is ARV 110, 120, 130, or 140.
Ensure you have the latest version of the use instructions to avoid complications during colonoscopy procedures.
The recall is due to updated instructions for use that may lead to complications during colonoscopy procedures if not followed correctly.
Endocuff Vision models ARV 110, 120, 130, and 140 distributed before May 1, 2020.
No, but you should review the updated instructions to ensure safe use during colonoscopy procedures.
We’ve drafted a message you can send Boddingtons Plastics to request your refund or repair — edit it as you like.
Subject: Recall Z-1718-2020 — Boddingtons Plastics Boddingtons Plastics Hello, I own a Boddingtons Plastics that is covered by recall Z-1718-2020 from Boddingtons Plastics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
