MAUDE Adverse Event Report: GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS) BD MAX¿ CTGCTV2 (US); MULTIPLE-TYPE SEXUALLY TRANSMITTED PATHOGEN NUCLEIC ACID IVD KIT

Catalog Number	443904
Medical Device Problem Code	False Negative Result (1225)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/02/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
D.2.Additional medical device types: mkz, ouy.Investigation summary: the complaint investigation for discrepant results when using the bd ctgctv2 for bd max¿ system (ref.(b)(4)) lot 4325960 was performed by the review of manufacturing records, review of customer¿s data and by the complaint¿s history review.Customer complained about a discrepant result for the trichomonas vaginalis (tv) target.Initial test gave a negative tv target result, while repeat test from the same sbt, but with another kit lot, gave a positive tv target result, both with bd ctgctv2 for bd max¿ system.Another sample from the same patient (collected at the same time with another swab), tested with the bd max¿ vaginal panel assay, gave a positive tv target result in two instances.The review of quality control records of bd ctgctv2 for bd max¿ system lot 4325960 revealed no anomalies that could explain the customer¿s discrepant result.Customer provided databases from bd max¿ instruments ct2342 and ct2473 for investigation.The customer identified the affected samples, which were analyzed.The first sample ((b)(6)), tested with the bd max¿ vaginal panel (vp), showed a positive tv result in both the initial run (position a6, run #(b)(4), ct2342) and the repeat run (position a6/run #(b)(4) with ct2473).The second sample ((b)(6)), tested with bd ctgctv2, initially gave a negative tv result (position b6, run #2125, ct2342).However, a repeat test performed on a third sample (b)(6) returned a positive tv result (position b1, run #(b)(4), ct2473), indicating a false negative (tv fn) discrepancy.Manual pcr curves adjudication for samples a6 (run 2125), a6 (run (b)(4)) and b1 (run (b)(4)) revealed late and low, but true, amplification for the tv target (fam channel bottom position of the cartridge for vaginal panel and cy5 channel for ctgctv2), while sample b6 (run 2125) showed no amplification for the tv target (cy5 channel for ctgctv2).Manual curve adjudication has limitations; visual examination of pcr curves for low signal is a conservative assessment of the data.Based on the data and information provided, specimens at or near the assay¿s limit of detection (lod), or environmental or cross-contamination are the most likely causes explaining the customer¿s discrepant results.Further analysis revealed same sbt was used on different instruments, however, based on ctgctv2 assay instruction for use, repeat testing from a single bd molecular sample buffer tube must be performed on the same bd max¿ system as the original test.Indeed, the instrument adjusts the pipetting height based on the number of tests performed with a single sbt.The root cause was not identified.There is no indication of a reagent issue based on the analysis of the complaints received for discrepant results on bd ctgctv2 for bd max¿ system lot 4325960.Bd cannot confirm the complaint based on the investigation that was performed.Bd did not initiate a corrective and a preventive action plan since no new hazard or trends was identified.Bd apologizes for the inconvenience that this may have caused.Bd quality will continue to monitor for trends.
Event or Problem Description
It was reported that during use of bd max¿ ctgctv2 (us), a false negative trichomonas vaginalis (tv) patient result was obtained.Sample tested tv positive on bd max¿ vaginal panel and tv negative on bd max¿ ctgctv2.There was no report of patient impact.

• Brand Name: BD MAX¿ CTGCTV2 (US)
• Common Device Name: MULTIPLE-TYPE SEXUALLY TRANSMITTED PATHOGEN NUCLEIC ACID IVD KIT
• Manufacturer (Section D): GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS); 2555 blv. du parc techn; quebec
• Manufacturer (Section G): GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS); 2555 blv. du parc techn; quebec
• Manufacturer Contact: matt j. connor ; 7 loveton circle; sparks, MD 21152 ; 4103164000
• MDR Report Key: 23707202
• Report Number: 3007420875-2025-00228
• Device Sequence Number: 10691714
• Product Code: LSL
• UDI-Device Identifier: 00382904439040
• UDI-Public: (01)00382904439040(17)260523(10)4325960
• Combination Product (Y/N): N
• Initial Reporter State: LA
• Initial Reporter Country: US
• PMA/510(K) Number: K182692
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 11/14/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Expiration Date: 05/23/2026
• Device Catalogue Number: 443904
• Device Lot Number: 4325960
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/14/2025
• Initial Report FDA Received Date: 12/03/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 01/21/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown