IMMULITE® 2000 Systems PTS PSA 10706282Recalls & reported problems
Siemens Healthcare Diagnostics Products Ltd · PTS PSA Kit 600 Test · Class 3
All models of IMMULITE 2000 Systems PTS PSA (2)
Data updated Oct 18, 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.
6 other recalls cover devices cleared under the same FDA submission (P930027); 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Sep 30, 2024Class IIOpen, Classified
The IMMULITE 2000 PSA assay for use on the IMMULITE 2000 and IMMULITE 2000 XPi analyzers did not meet the High-dose Hook Effect claim as stated in the Instructions for Use (IFU).
Z-0464-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under P930027. One submission often covers many models, so check the product and lot details in each record.
- Z-1119-2017 · Dec 21, 2016 · TerminatedIMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LKUP1, SMN 10380956 (OUS Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE and IMM
- Z-1120-2017 · Dec 21, 2016 · TerminatedIMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LK3PS1, SMN 10706293 (US Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE and IMM
- Z-0884-2017 · Nov 18, 2016 · TerminatedIMMULITE/IMMULITE 1000 Systems Prostate-Specific Antigen (PSA) Assay, REF/Catalog Number LKPTS1, Siemens Material Number (SMN) 10706279 (US); Catalog Number LKPS1, SMN 10380960 and
- Z-0885-2017 · Nov 18, 2016 · TerminatedIMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA) Assay, REF/Catalog Number L2KPTS2, SMN 10706281 and REF/Catalog Number L2KPTS6, SMN 10706282 (US); REF/Catal
- Z-2047-2013 · Jun 26, 2013 · TerminatedPSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers, Catalog Numbers LKPS1, LKPS5 and LKPTS1(D); and in the IMMULITE 2000/2000XPi Systems Analyzers, Catalog Numbers
- Z-2090-2008 · May 21, 2008 · TerminatedCOAT-A-COUNT PSA IRMA kit (IKPS1, 2, 5, X). The device is intended as an aid in monitoring patients for disease progress or response to therapy.
Other Total,Prostate Specific Antigen(Noncomplexed&Complexed) For Detection Of Prostate Cancer devices
- IMMULITE® 2000 Systems PTS PSA 10706281Siemens Healthcare Diagnostics Products Ltd · Total,Prostate Specific Antigen(Noncomplexed&Complexed) For Detection Of Prostate Cancer1 recall1 report
- Elecsys total PSA 08791732190Roche Diagnostics GmbH · Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer48 reports
- Dimension Vista® System TPSA Flex® Reagent Cartridge 10445090Siemens Healthcare Diagnostics Inc. · Total,Prostate Specific Antigen(Noncomplexed&Complexed) For Detection Of Prostate Cancer36 reports
- Dimension® clinical chemistry system TPSA Flex® reagent cartridge 10444889Siemens Healthcare Diagnostics Inc. · Total,Prostate Specific Antigen(Noncomplexed&Complexed) For Detection Of Prostate Cancer12 reports
- Elecsys Total PSA 09744860190Roche Diagnostics GmbH · Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer4 reports
- Elecsys total PSA 08791686160Roche Diagnostics GmbH · Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer3 reports
- Elecsys total PSA 07027966190Roche Diagnostics GmbH · Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer3 reports
- Access Hybritech PSA 37200Beckman Coulter, Inc. · Total,Prostate Specific Antigen(Noncomplexed&Complexed) For Detection Of Prostate Cancer3 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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