Centurion BT235ARecalls & reported problems
Centurion Medical Products Corporation · BIOPSY/ASPIRATION TRAY · Class 1
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 18, 2023Open, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2199-2023 · Root cause: Device Design · FDA record ↗
- May 15, 2023Open, Classified
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Z-2322-2023 · Root cause: Nonconforming Material/Component · FDA record ↗
Other TRAY, SURGICAL devices
- Centurion MNS11625Centurion Medical Products Corporation · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDA2526Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1470BMedline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1534Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE CVI4830AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYKM1730AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYKM1927AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- Centurion MNS11590Centurion Medical Products Corporation · TRAY, SURGICAL2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.