Centurion MNS12590Recalls & reported problems
Centurion Medical Products Corporation · PRECIP TRAY · Class 1
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Mar 3, 2025Open, Classified
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Z-1603-2025 · Root cause: Under Investigation by firm · FDA record ↗
Other TRAY, SURGICAL devices
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- 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.