CARDINAL HEALTH SNECNNPOLGRecalls & reported problems
Cardinal Health 200, LLC · NEURO PACK · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888439382891), received between Jul 24, 2019 and Jul 24, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Nov 8, 2024Class IIOpen, Classified
Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
Z-1134-2025 · Root cause: Material/Component Contamination · Recall details · FDA record ↗
Most reported problems
Device problems
- Material Integrity Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 24, 2019Material Integrity Problem
THE CUSTOMER REPORTED THAT THE OR TOWEL (CATALOG# PWTB04-STM) IN THEIR NEURO PACK (CATALOG# SNECNNPOLG) APPEARED TO BE ¿LINTY¿ DURING A MICRODISCECTOMY. MANUAL REMOVAL AND IRRIGATION WERE NEEDED WHICH LED TO A TEN MINUTE DELAY IN THE PROCEDURE. NO ADVERSE EFFECTS TO THE PATIENT ARE KNOWN AT THIS TIME.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8823391 ↗
Other Neurological tray devices
- Medline Industries, Inc. DYNJ61157CMedline Industries, Inc. · Neurological tray5 recalls0 reports
- Medline Industries, Inc. DYNJ42844DMedline Industries, Inc. · Neurological tray5 recalls0 reports
- Medline Industries, Inc. DYNJ58704AMedline Industries, Inc. · Neurological tray4 recalls0 reports
- Medline Industries, Inc. DYNJ909744Medline Industries, Inc. · Neurological tray4 recalls0 reports
- Medline Industries, Inc. DYNJ53799Medline Industries, Inc. · Neurological tray4 recalls0 reports
- Medline Industries, Inc. DYNJ40040CMedline Industries, Inc. · Neurological tray4 recalls0 reports
- Medline Industries, Inc. DYNJ35349CMedline Industries, Inc. · Neurological tray4 recalls0 reports
- Medline Industries, Inc. CDS981327QMedline Industries, Inc. · Neurological tray4 recalls0 reports
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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page