RUSCH IPN040900Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04026704002672), received between Feb 15, 2022 and Feb 15, 2022 — classified as 1 malfunction.

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

7 other recalls cover devices cleared under the same FDA submission (K935842); they may or may not involve this specific model.

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 15, 2022Deflation Problem; Deflation Problem

  IT WAS REPORTED THAT "THE INNER CUFF DID NOT DEFLATE DURING A TEST BEFORE USE". NO PATIENT INVOLVEMENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13534330 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K935842. One submission often covers many models, so check the product and lot details in each record.

• Z-2533-2020 · May 29, 2020 · Terminated
  RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D
• Z-1685-2019 · Apr 1, 2019 · Terminated
  RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0
• Z-1686-2019 · Apr 1, 2019 · Terminated
  RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0
• Z-1683-2019 · Apr 1, 2019 · Terminated
  RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
• Z-1684-2019 · Apr 1, 2019 · Terminated
  RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
• Z-1682-2019 · Apr 1, 2019 · Terminated
  RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0
• Z-1851-2014 · May 23, 2014 · Terminated
  RUSCH, LaserTube (Rubber), Laser Resistant Tracheal Tube, cuffed, Teleflex Medical, Willy-Rusch, GmbH. A tracheal tube is a device inserted into a patient's trachea via the n