MAUDE Adverse Event Report: A.I.D.D LONGFORD ARCHITECT TOTAL B-HCG REAGENT KIT; SYSTEM, TEST, HUMAN CHORIONIC GONADOTROPIN

Model Number	7K78-30
Medical Device Problem Code	False Positive Result (1227)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	10/27/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
An evaluation is in process.A follow-up report will be submitted when the evaluation is complete.No additional patient information is available.Full zip code is (b)(6).
Event or Problem Description
The customer generated false positive architect total b-hcg results for one patient.The following information was provided: sid (b)(6), initial test result: 3444.02 miu/ml.Retest result: <1.2 miu/ml.Patient is female without pregnancy reactions.No impact to patient management was reported.
Additional Manufacturer Narrative
A review of tickets was performed for reagent lot number 11237ui00.The ticket search determined that there is elevated complaint activity for the likely cause lot.A review of tracking and non-statistical trending did not identify trends for the complaint issue.Return testing was not completed as returns were not available.Accuracy testing protocol was executed using retained samples of the reagent lot, all validity and acceptance criteria were met.A review of the manufacturing documentation did not identify any issues associated with the complaint issue.A review of labeling concluded that the issue is sufficiently addressed.Based on the investigation no systemic issue or deficiency of the architect total b-hcg for lot 11237ui00 was identified.
Additional Manufacturer Narrative
Previously submitted report# 3005094123-2020-00249-01 inadvertently populated g4 as 10/27/2020.The correct date was 12/15/2020.

• Brand Name: ARCHITECT TOTAL B-HCG REAGENT KIT
• Common Device Name: SYSTEM, TEST, HUMAN CHORIONIC GONADOTROPIN
• Manufacturer (Section D): A.I.D.D LONGFORD; lisnamuck; co. longford; longford N39E9 32; EI N39E932
• MDR Report Key: 10801712
• Report Number: 3005094123-2020-00249
• Device Sequence Number: 2953547
• Product Code: DHA
• UDI-Device Identifier: 00380740014971
• UDI-Public: 00380740014971
• Combination Product (Y/N): N
• PMA/510(K) Number: K983424
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 01/06/2021

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: Health Professional
• Device Expiration Date: 01/06/2021
• Device Model Number: 7K78-30
• Device Catalogue Number: 07K78-30
• Device Lot Number: 11237UI00
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 10/27/2020
• Supplement Date Received by Manufacturer: 10/27/2020; 01/06/2021
• Initial Report FDA Received Date: 11/06/2020
• Supplement Report FDA Received Date: 12/28/2020; 01/06/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: ARC I2000SR INST, 03M74-02, ISR63846; ARC I2000SR INST, 03M74-02, ISR63846; ARC I2000SR INST, 03M74-02, ISR63846