MAUDE Adverse Event Report: IMMUCOR, INC. PANOSCREEN I AND II - 2 VIAL SET; REAGENT RED BLOOD CELLS

Catalog Number	0002380
Medical Device Problem Code	False Negative Result (1225)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	02/07/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Immucor technical support interviewed the customer site on (b)(4) 2019 about the manual test tube testing.The immucor internal report record number for this report is (b)(4).
Event or Problem Description
On (b)(6) 2019, a (b)(6) customer site reported an unexpectedly negative antibody screen when tested with test tubes, when tested on (b)(6) 2019.

• Brand Name: PANOSCREEN I AND II - 2 VIAL SET
• Common Device Name: REAGENT RED BLOOD CELLS
• Manufacturer (Section D): IMMUCOR, INC.; 3130 gateway drive; norcross GA 30091 5625
• MDR Report Key: 8412970
• Report Number: 1034569-2019-00055
• Device Sequence Number: 2228044
• Product Code: KSZ
• UDI-Device Identifier: 10888234000297
• UDI-Public: 10888234000297
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: 102707/0.0
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,u
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/12/2019

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: No Information
• Device Catalogue Number: 0002380
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/13/2019
• Initial Report FDA Received Date: 03/12/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1