CARDINAL HEALTH CHLOT01-08Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885380101588), received between Jul 12, 2021 and Jul 12, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Open or Close” (1 report).

1 other recall cover devices cleared under the same FDA submission (K132243); 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 18, 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.

• MalfunctionJul 12, 2021Difficult to Open or Close

  PATIENT WITH HISTORY OF ENDOMETRIAL CANCER WAS ADMITTED FOR A RIGHT CHEST PORT PLACEMENT. WHEN OPENING THE CARDINAL HEALTH 200, LLC OCTYL TOPICAL SKIN ADHESIVE, DOME TIP, 0.8ML, THE SKIN GLUE WOULD NOT OPEN. NO GLUE WOULD COME OUT. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12149130 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K132243. One submission often covers many models, so check the product and lot details in each record.

• Z-1788-2022 · May 25, 2022 · Open, Classified
  a. Skin Adhesive McKesson LiquiBand Exceed 0.4 mL Liquid Dome Applicator Tip 2-Octyl Cyanoacrylate. Model Number: 122-LBXS. b. Skin Adhesive McKesson LiquiBand Exceed 0.8 mL Liqui