Clearview™ 22120Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20643169888672), received between Mar 27, 2024 and Aug 22, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Mar 19, 2024Open, Classified

   Potential for unsealed sterile packing.

   Z-1794-2024 · Root cause: Process control · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 22, 2024Obstruction of Flow; Obstruction of Flow

  MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A CLEARVIEW BLOWER MISTER, IT WAS REPORTED THAT NO CO2 GAS CAME OUT. THE DEVICE WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT NONE OF THE DEVICE TUBING OR THE DISTAL TIP APPEARED TO BE DAMAGED OR OCCLUDED. THERE WAS NO DAMAGE OR KINK IN THE TUBING. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE CUSTOMER THINKS THE TIP WAS ON THE DEVICE WHEN THEY USED IT BUT THEY ARE NOT CERTAIN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20026707 ↗
• MalfunctionMar 27, 2024Break; Break

  MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A CLEARVIEW BLOWER/MISTER, IT WAS REPORTED THAT THE IV PART OF THE DEVICE WAS BROK EN. USE OF THE DEVICE WAS UNSPECIFIED. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18985131 ↗