DeRoyal 47-670Recalls & reported problems
Deroyal Industries, Inc. · ST NEONATAL DRG CHG KIT 50C · Class 1
- 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.
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.
Recalls naming this device
- Mar 3, 2022Terminated
A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.
Z-0878-2022 · Root cause: Process control · FDA record ↗
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- Centurion Medical Products Corp DT22065Medline Industries, Inc. · Dressing change tray2 recalls0 reports
- MEDLINE CVI4770AMedline Industries, Inc. · Dressing change tray2 recalls0 reports
- Centurion DT18700Centurion Medical Products Corporation · Dressing change tray2 recalls0 reports
- Centurion DM1035ACenturion Medical Products Corporation · Dressing change tray2 recalls0 reports
- Centurion DM1035Centurion Medical Products Corporation · Dressing change tray2 recalls0 reports
- MEDLINE EBSI1498Medline Industries, Inc. · Dressing change tray2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.