CODMAN 24-5408Recalls & reported problems
Cerenovus, Inc. · CODMAN Bulk Surgical Patties X-Ray Detectable 1/2 Inch x 1 1/2 Inches (1.27cm x 3.81cm) · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 20886704004179), received between Jul 31, 2018 and Jul 31, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Missing” (1 report).
3 other recalls cover devices cleared under the same FDA submission (K880402); 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Component Missing1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 31, 2018Component Missing; Component Missing
AS REPORTED BY THE DISTRIBUTOR, A PACK OF CODMAN PATTIES HAD ONE SPONGE MISSING A STRING. PATTIE PACK WAS PULLED FROM STOCK. THERE WERE NO REPORTS OF DELAY OR PATIENT HARM.
Patient problems: No Patient Involvement
MAUDE report 7735303 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K880402. One submission often covers many models, so check the product and lot details in each record.
- Z-0093-2011 · Jul 16, 2010 · TerminatedCodman 5/16" Round Surgical Patties (20 pouches of 10 patties per box) Product code: 80-1396
- Z-0094-2011 · Jul 16, 2010 · TerminatedCodman 1/4 x 1/4" Surgical Patties (20 pouches of 10 patties per box) Product code: 80-1399
- Z-0095-2011 · Jul 16, 2010 · TerminatedSurgical Pattie, 1/4" x 1/4" Non--Sterile (Each Unit of sales is 100 cards) of patties on each card) Product code: 24-5403
Other NEUROSURGICAL PADDIE devices
- CODMAN® 801400Integra Lifesciences Production Corporation · Neurosurgical paddie2 recalls9 reports
- CODMAN® 801407Integra Lifesciences Production Corporation · Neurosurgical paddie1 recall6 reports
- MEDLINE NEUROSPNG05Medline Industries, Inc. · Neurosurgical paddie1 recall5 reports
- CODMAN® 801451Integra Lifesciences Production Corporation · Neurosurgical paddie1 recall5 reports
- CODMAN® 801404Integra Lifesciences Production Corporation · Neurosurgical paddie1 recall4 reports
- CODMAN® 801406Integra Lifesciences Production Corporation · Neurosurgical paddie1 recall2 reports
- CODMAN® 801403Integra Lifesciences Production Corporation · Neurosurgical paddie1 recall2 reports
- CODMAN 80-1407Cerenovus, Inc. · NEUROSURGICAL PADDIE1 recall2 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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