MAUDE Adverse Event Report: DEVICOR MEDICAL PRODUCTS, INC. MAMMOTOME ELITE BIOPSY PROBE; BIOPSY INSTRUMENT

Model Number	MEP13
Medical Device Problem Codes	Failure to Obtain Sample (2533); Output Problem (3005)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	05/29/2018
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Mep13 probes are sterile, single use devices, indicated to obtain tissue samples from the breast or axillary lymph nodes for diagnostic analysis of breast abnormalities.One mep13 probe from lot # f1183310d was received in fair condition.Use in a procedure was evident on the probe.The was probe connected to a holster for functional evaluation.Using chicken breast as a medium, the device was unable to obtain samples.Further visual inspection found breast tissue clogged in the device cutter.Once the cutter was cleared, the device obtained samples as designed.The customer holster was not returned for evaluation.Based on product knowledge, the reported event could be caused by a lack of vacuum.Without a customer holster, a root cause cannot be confirmed.
Event or Problem Description
Devicor medical products, inc.Has received a report from the sales representative stating, "during procedure mep13 probe did not pick up samples.Procedure was completed with another device".This has been documented in our complaint system as record # (b)(4).

• Brand Name: MAMMOTOME ELITE BIOPSY PROBE
• Common Device Name: BIOPSY INSTRUMENT
• Manufacturer (Section D): DEVICOR MEDICAL PRODUCTS, INC.; 300 e. business way; fifth floor; cincinnati OH 45241
• MDR Report Key: 7850143
• Report Number: 3008492462-2018-00069
• Device Sequence Number: 2725800
• Product Code: KNW
• UDI-Device Identifier: 00841911100898
• UDI-Public: (01)00841911100898(17)220402(10)F11813310D
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K153709
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/30/2018

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: 04/02/2022
• Device Model Number: MEP13
• Device Catalogue Number: MEP13
• Device Lot Number: F11813310D
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/05/2018
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/21/2018
• Initial Report FDA Received Date: 09/06/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1