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Clean W-203-B(EC)Recalls & reported problems

Guangzhou Clean Medical Products Manufacturing Corp. · Disposable Electronically Pulsed Lavage Suction Apparatus · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06951233720279), received between Apr 23, 2022 and Apr 23, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Delivered as Unsterile Product” (1 report).

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.

Most reported problems

Device problems

  • Delivered as Unsterile Product1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionApr 23, 2022Delivered as Unsterile Product; Delivered as Unsterile Product

    IT WAS REPORTED THAT, WHEN OPENING A VERSAPULSE-DISPOSABLE PULSE LAVAG SUCTION BOX DURING THE SET-UP FOR A TKA SURGERY, IT WAS FOUND THAT BOTH STERILE PACKAGING HAD BEEN OPENED ALREADY. SURGERY WAS RESUMED, WITHOUT ANY DELAY, WITH A COMPETITOR'S DEVICE (PULSE LAVAGE FROM ZIMMER - PULSAVAC). PATIENT WAS NOT INJURED AS CONSEQUENCE OF THIS PROBLEM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14191097 ↗

Other Lavage, Jet devices

All Lavage, Jet devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.