CARDINAL HEALTH SNE81ULNMORecalls & reported problems
Cardinal Health 200, LLC · UNIVERSAL LAMINECTOMY PACK · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 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 16, 2026.
Recalls naming this device
- Nov 8, 2024Open, 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 ↗
- Aug 16, 2023Open, Classified
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Z-0089-2024 · Root cause: Material/Component Contamination · Recall details · FDA record ↗
Other Neurological tray devices
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- Medline Industries, Inc. DYNJ61157CMedline Industries, Inc. · Neurological tray5 recalls0 reports
- Medline Industries, Inc. DYNJ60792CMedline Industries, Inc. · Neurological tray4 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. DYNJ21925SMedline 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
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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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