Medivators recalls Endo SmartCap Tubing (REF CPK-100222-0002) due to potential inadequate insufflation, air bubbles, or water leaks during endoscopic procedures. Affected units may cause procedure complications.
Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly that may present during procedures as inadequate insufflation, presence of air bubbles inside the endo smartcap tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve.
Medivators is recalling Endo SmartCap Tubing because it may not work properly during endoscopic procedures. This could lead to air bubbles, insufficient water for rinsing, or leaks that might cause procedure complications.
The tubing may not provide enough air or CO2 during procedures, leading to air bubbles in the tubing, insufficient water to rinse the endoscope lens, or water leaking from the air/water valve. This could cause procedure complications if the tubing fails during use.
Endoscopists and medical professionals using the Endo SmartCap Tubing for procedures are most at risk. Patients undergoing endoscopic procedures with this tubing may experience complications.
Check for the product name 'Endo SmartCap Tubing' and the reference number CPK-100222-0002. The tubing was sold with endoscopes for procedures requiring air or CO2.
Inspect the tubing for air bubbles or water leaks that could indicate improper function.
Confirm the product reference number CPK-100222-0002 to ensure it matches the recalled item.
The recall states the tubing may not work properly during procedures, so it is not recommended for use until the issue is resolved.
The recall does not specify a remedy, so contact Medivators directly for guidance.
The recall indicates potential issues during procedures, so it is advised to stop using it until the problem is addressed.
We’ve drafted a message you can send Medivators to request your refund or repair — edit it as you like.
Subject: Recall Z-1778-2020 — Medivators Medivators Hello, I own a Medivators that is covered by recall Z-1778-2020 from Medivators. 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.
