MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 4.0MM CANNULATED SCREW-LONG THREAD 52MM; SCREW, FIXATION, BONE

Model Number	207.752
Medical Device Problem Code	Crack (1135)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	11/08/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Complainant part is not expected to be returned for manufacturer review / investigation.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.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 during an unknown procedure on (b)(6) 2019, the doctor decided to power the 4.0 cannulated screw in, and the thread of screw scuffled and kind of unwound, and spun all over.The was able to be retrieved from the patient and then another screw was put in.The procedure and patient outcome are unknown.Concomitant devices: handpiece powered driver (part: unknown, lot: unknown, quantity: 1).This report is for a 4.0 mm cannulated screw 52 mm.This is report 1 of 1 for (b)(4).

• Brand Name: 4.0MM CANNULATED SCREW-LONG THREAD 52MM
• Common Device Name: SCREW, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 9377696
• Report Number: 2939274-2019-62396
• Device Sequence Number: 3103753
• Product Code: HWC
• UDI-Device Identifier: 10886982148568
• UDI-Public: (01)10886982148568
• Combination Product (Y/N): N
• Initial Reporter State: NE
• Initial Reporter Country: US
• PMA/510(K) Number: K161616
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 11/08/2019

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: Health Professional
• Device Model Number: 207.752
• Device Catalogue Number: 207.752
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 11/08/2019
• Initial Report FDA Received Date: 11/26/2019
• Patient Sequence Number: 1