CARDINAL HEALTH 30414-025Recalls & reported problems
Cardinal Health 200, LLC · PENROSE DRAIN 12" X 1/4 · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885425501809), received between Oct 25, 2022 and Nov 14, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Damaged Prior to Use” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device Damaged Prior to Use1
- Manufacturing, Packaging or Shipping Problem1
- Material Disintegration1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 14, 2022Material Disintegration; Device Damaged Prior to Use
UNOPENED PENROSE DRAIN WITH HOLES OR DRY ROT IN THE DRAIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15787662 ↗MalfunctionOct 25, 2022Manufacturing, Packaging or Shipping Problem
UNOPENED PACK WITHOUT PRODUCT IN THE PACKAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15665648 ↗
Other CATHETER, PERITONEAL devices
- ARROW IPN036986Teleflex Incorporated · CATHETER, PERITONEAL2 recalls0 reports
- ARROW IPN032635Teleflex Incorporated · CATHETER, PERITONEAL2 reports
- Super Sheath CBDE (CBDE) CI12L25TP0038Togo Medikit CO.,Ltd. · CATHETER, PERITONEAL1 report
- Tenckhoff G09085Cook Incorporated · CATHETER, PERITONEAL1 report
- Cook G05262Cook Incorporated · CATHETER, PERITONEAL1 report
- Cook G05267Cook Incorporated · CATHETER, PERITONEAL1 report
- Medline DYND50428Medline Industries, Inc. · CATHETER, PERITONEAL1 report
- Cook G09269Cook Incorporated · CATHETER, PERITONEAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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