Centurion DYNDC2356BRecalls & reported problems
Centurion Medical Products Corporation · CENTRAL LINE DRESSING SV43 FCP · Class 1
Data updated Oct 16, 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
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
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 16, 2026.
Recalls naming this device
- Apr 27, 2026Open, Classified
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Z-2437-2026 · Root cause: Process control · Recall details · FDA record ↗
Other Dressing change tray devices
- MEDLINE EBSI1498Medline Industries, Inc. · Dressing change tray2 recalls0 reports
- Centurion DT8670ACenturion Medical Products Corporation · Dressing change tray2 recalls0 reports
- Centurion Medical Products Corp DT22065Medline Industries, Inc. · Dressing change tray2 recalls0 reports
- Centurion DT21275Centurion Medical Products Corporation · Dressing change tray2 recalls0 reports
- MEDLINE EBSI1382Medline Industries, Inc. · Dressing change tray2 recalls0 reports
- Centurion DM1035Centurion Medical Products Corporation · Dressing change tray2 recalls0 reports
- Centurion DT18700Centurion Medical Products Corporation · Dressing change tray2 recalls0 reports
- MEDLINE EBSI1464Medline Industries, Inc. · Dressing change tray2 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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