MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC HAMMERLOCK 2 IMPLANT KIT 12X5MM/0 DEGREES/SMALL; INTRAMEDULLARY BONE FASTENER

Model Number	HL2S
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Code Available (3191)
Date of Event	01/25/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Initial reporter is synthes sales representative.Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.(b)(4).Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
It was reported that on an unknown date, the bme hammerlock 2 implant kit broke off of the handle and switched the bme for k wire.The patient had extremely hard bone and the doctor was pushing very hard on the device while inserting and it was believe the tension caused the insertion handle to break off of the implant.She did drill and use the 1 and 2 broach.There was a surgical delay of 5 minutes.The procedure was successfully completed.Patient status is unknown.This report is for one (1) hammerlock 2 implant kit 12x5mm/0 degrees/small.This is report 1 of 1 for (b)(4).
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
The procedure occurred on (b)(6) 2019.There was no patient consequence.

• Brand Name: HAMMERLOCK 2 IMPLANT KIT 12X5MM/0 DEGREES/SMALL
• Common Device Name: INTRAMEDULLARY BONE FASTENER
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 8339396
• Report Number: 2939274-2019-56446
• Device Sequence Number: 19367411
• Product Code: HTY
• UDI-Device Identifier: 00810633021484
• UDI-Public: (01)00810633021484
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K133520
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 01/25/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: HL2S
• Device Catalogue Number: HL2S
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 01/25/2019
• Supplement Date Received by Manufacturer: 03/26/2019
• Initial Report FDA Received Date: 02/14/2019
• Supplement Report FDA Received Date: 03/27/2019
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention