MAUDE Adverse Event Report: DEPUY MITEK HEALIX 5.5 TI 3 W/ORTHOCORD; SOFT-TISSUE ANCHOR, NON-BIOABSORBABLE

Catalog Number	222243
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	03/11/2016
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.The complaint device is not being returned.A batch record review has been conducted to determine if there were any internal processing issues which would have contributed to the nature of the product complaint.Our results indicate that this batch of product was processed without incident and therefore there is no internally assignable cause for the reported problem.Further, a review into the depuy synthes mitek complaints system revealed a similar complaint for this lot released to distribution.We cannot discern a root cause for the reported failure mode.Upon review the lot it was discerned that the customer used the product on a patient after the product's expiration date.The product was not left in the patient and was discarded.There were no adverse patient consequences reported at the time the complaint was reported.Should depuy synthes mitek be made aware of any future adverse patient consequences resulting from the use of this device after its expiration date, this complaint will be reopened and the complaint will be updated to reflect the new information.No corrective action is required and no further action is warranted at this time.This file will remain receptive to any potential forthcoming information received that is pertinent and germane to this issue.However, 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.Udi: (b)(4).This report is being filed from the etq complaint management system as required under mitek's corrective and preventative actions (capa) to file usa fda mdr missed malfunctions.
Event or Problem Description
It was reported by the sales rep that during an unspecified surgical procedure of the shoulder repair, it was observed that the back or proximal end of the customer's healix ti anchor 5.5mm with 3 suture orthocord & needles broke off during insertion.The sales rep reported that the surgeon did not drill and just used the healix punch to prepare the bone tunnel.The sales rep reported that the surgeon removed the broken pieces and completed the procedure with another same type anchor in the same bone hole.The sales rep reported that the surgeon was satisfied with the fixation.The sales rep reported that the patient was young and had very hard bone.There were no patient consequences or delays reported.All available information has been disclosed.If additional information should become available, a supplemental medwatch will be submitted accordingly.

• Brand Name: HEALIX 5.5 TI 3 W/ORTHOCORD
• Common Device Name: SOFT-TISSUE ANCHOR, NON-BIOABSORBABLE
• Manufacturer (Section D): DEPUY MITEK; 325 paramount drive; raynham MA 02767
• MDR Report Key: 7677130
• Report Number: 1221934-2018-51715
• Device Sequence Number: 19220882
• Product Code: HWC
• UDI-Device Identifier: 10886705007899
• UDI-Public: 10886705007899
• Combination Product (Y/N): N
• Initial Reporter State: ID
• Initial Reporter Country: US
• PMA/510(K) Number: K082282
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/11/2016

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: 12/30/2015
• Device Catalogue Number: 222243
• Device Lot Number: 3662322
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 03/11/2016
• Initial Report FDA Received Date: 07/11/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): Yes
• Patient Sequence Number: 1