MAUDE Adverse Event Report: VENTANA MEDICAL SYSTEMS INC. CONFIRM ANTI-ESTROGEN RECEPTOR (ER) (SP1) RABBIT MONOCLONAL PRIMARY ANTIBODY; IMMUNOHISTOCHEMISTRY ANTIBODY ASSAY, ESTROGEN RECEPTOR

Catalog Number	05278414001
Medical Device Problem Codes	False Negative Result (1225); Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	11/26/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The serial number of the analyzer is (b)(6).The investigation is ongoing.
Event or Problem Description
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.
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.

• Brand Name: CONFIRM ANTI-ESTROGEN RECEPTOR (ER) (SP1) RABBIT MONOCLONAL PRIMARY ANTIBODY
• Common Device Name: IMMUNOHISTOCHEMISTRY ANTIBODY ASSAY, ESTROGEN RECEPTOR
• Manufacturer (Section D): VENTANA MEDICAL SYSTEMS INC.; 1910 e innovation park dr; tucson AZ 85755
• Manufacturer (Section G): VENTANA MEDICAL SYSTEMS INC.; 1910 e innovation park dr; tucson AZ 85755
• Manufacturer Contact: natalie catton ; 9115 hague road; indianapolis, IN 46250 ; 9253534412
• MDR Report Key: 23838220
• Report Number: 2028492-2025-05193
• Device Sequence Number: 20081851
• Product Code: MYA
• UDI-Device Identifier: 04015630972234
• UDI-Public: 04015630972234
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K110215
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 01/12/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 05278414001
• Device Lot Number: ASKU
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 11/26/2025
• Supplement Date Received by Manufacturer: 12/18/2025
• Initial Report FDA Received Date: 12/18/2025
• Supplement Report FDA Received Date: 01/12/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown