MAUDE Adverse Event Report: MEDOS INTERNATIONAL SÃ RL INTRAFX ADV POLYPROSHTHLG 30MM; SOFT-TISSUE ANCHOR, NON-BIOABSORBABLE

Catalog Number	254826
Medical Device Problem Code	Device Markings/Labelling Problem (2911)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Udi: (b)(4).
Event or Problem Description
It was reported by the sales rep that he received a large 30 mm intrafix advance sheath with blue labeling instead of purple labeling.There was no patient or case involvement.The device is not being returned.The sales rep provide a picture.
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.The complaint device is not being returned and is therefore unavailable for a physical evaluation.Pictures were provided which have been analyzed to confirm the complaint.A non-conformance search was performed for this part/lot combination and two non-conformances were identified.According to the investigation, there is a non-medical impact to the device as the intrafix advance system instrumentation and implants are color coded by size.This issue may cause difficulty in identifying the correct size sheath.Functionality of the product is not impacted by this issue.Depuy synthes mitek will continue to track any related complaints within this device family as a means of monitoring the extent with which this complaint is observed in the field.(b)(4).

• Brand Name: INTRAFX ADV POLYPROSHTHLG 30MM
• Common Device Name: SOFT-TISSUE ANCHOR, NON-BIOABSORBABLE
• Manufacturer (Section D): MEDOS INTERNATIONAL SÃ RL; chemin-blanc 38; le locle CH-24 00; SZ CH-2400
• MDR Report Key: 7490481
• Report Number: 1221934-2018-50569
• Device Sequence Number: 1417264
• Product Code: MBI
• UDI-Device Identifier: 10886705027538
• UDI-Public: 10886705027538
• Combination Product (Y/N): N
• Initial Reporter State: UT
• Initial Reporter Country: US
• PMA/510(K) Number: K160804
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Health Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/18/2018

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: 05/31/2020
• Device Catalogue Number: 254826
• Device Lot Number: L434132
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 04/18/2018
• Supplement Date Received by Manufacturer: 10/25/2018
• Initial Report FDA Received Date: 05/07/2018
• Supplement Report FDA Received Date: 10/28/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1