CONFIRM ANTI-ESTROGEN RECEPTOR (ER) (SP1) RABBIT MONOCLONAL PRIMARY ANTIBODY
Received Dec 18, 2025 · Event occurred Nov 26, 2025
Report 2028492-2025-05193 · MDR key 23838220
Device
Generic name
Immunohistochemistry Antibody Assay, Estrogen Receptor
Manufacturer
Ventana Medical Systems Inc.Catalog number
05278414001
Lot number
ASKU
Product problems
- False Negative Result
- Incorrect, Inadequate or Imprecise Result or Readings
- False Negative Result
- Incorrect, Inadequate or Imprecise Result or Readings
Patient
NA · Unknown
- Insufficient Information
- Insufficient Information
Narrative
Additional Manufacturer Narrative
DESPITE MULTIPLE ATTEMPTS, NO FURTHER INFORMATION RELATED TO THE PATIENT, INCLUDING CURRENT CONDITION, ANY DELETERIOUS EFFECTS, AND DIAGNOSTIC DECISIONS BASED ON THE ASSAY RESULTS, COULD BE OBTAINED. DETAILS REGARDING REPEAT TESTING PRACTICES, SAMPLE COLLECTION, LOT NUMBERS, PROTOCOLS, AND CONTROL USAGE WERE REQUESTED BUT REMAIN UNKNOWN. A PRELIMINARY INTERNAL INVESTIGATION REVEALED A REDUCTION IN TUMOR STAIN INTENSITY AND PERCENT TUMOR CELL STAINING IN WEAK-STAINING BREAST CARCINOMA CASES WHEN TESTING SPECIFIC BATCHES OF RAW MATERIAL. CURRENT RAW MATERIAL BATCHES UTILIZED IN THE PRODUCTION OF FINISHED GOODS SHOW NO EVIDENCE OF LIGHT STAINING. ROCHE HAS ADVISED CUSTOMERS TO DISCONTINUE THE USE OF AND DISCARD ANY REMAINING INVENTORY OF THE AFFECTED 11 REAGENT LOTS. THE ISSUE WOULD NOT CAUSE ADVERSE HEALTH CONSEQUENCES WHEN THE EXTERNAL POSITIVE CONTROL TISSUES AND STAINING PROCEDURES ARE USED, AS RECOMMENDED IN THE PRODUCT METHOD SHEET, WHICH STATES THAT A POSITIVE TISSUE CONTROL MUST BE RUN WITH EACH RUN AND CAP/CLIA GUIDELINES ARE FOLLOWED. THE RESULTS ARE INTERPRETED BY A QUALIFIED PATHOLOGIST IN CONJUNCTION WITH HISTOLOGICAL EXAMINATION AND RELEVANT CLINICAL INFORMATION TO DETECT INAPPROPRIATE CELL STAINING ON KNOWN CONTROL TISSUES AND INTERNAL CONTROL CELLS, PER THE PRODUCT METHOD SHEET. MITIGATING FACTORS INCLUDE THE USE OF RECOMMENDED EXTERNAL POSITIVE CONTROL TISSUES (A WEAKLY POSITIVE BREAST CARCINOMA), USING ER IN CONJUNCTION WITH PR, AND ASSESSING ER STATUS IN THE CONTEXT OF CLINICAL HISTORY AND TUMOR MORPHOLOGY.
Additional Manufacturer Narrative
THE SERIAL NUMBER OF THE ANALYZER IS (B)(6). THE INVESTIGATION IS ONGOING.
Description of Event or Problem
THERE WAS AN ALLEGATION OF DISCREPANT RESULTS WITH THE CONFIRM ANTI-ESTROGEN RECEPTOR (ER) (SP1) RABBIT MONOCLONAL PRIMARY ANTIBODY ASSAY FOR A PATIENT SAMPLE TESTED ON A BENCHMARK ULTRA STAINER MODULE. THE INITIAL RESULT WAS ER NEGATIVE. THE REPEAT RESULT WAS MODERATE ER POSITIVE. THE PATIENT WAS DIAGNOSED AS TRIPLE NEGATIVE BREAST CANCER (TNBC). WITH THE UPDATED ER-POSITIVE RESULT, IT IS REPORTED THAT THE PATIENT WOULD BE ELIGIBLE FOR HORMONE THERAPY. DESPITE MULTIPLE ATTEMPTS, NO FURTHER INFORMATION RELATED TO THE PATIENT, INCLUDING CURRENT CONDITION, ANY DELETERIOUS EFFECTS, AND DIAGNOSTIC DECISIONS BASED ON THE ASSAY RESULTS, COULD BE OBTAINED.