FDA Adverse Event Malfunction Summary report: N

TI COLLAR WITH GROOVES

MDR report key: 3013529 · Received March 20, 2013

Report

Report Number
2530088-2013-10262
Event Type
Malfunction
Date Received
March 20, 2013
Date of Event
February 22, 2012
Report Date
February 22, 2012
Manufacturer
SYNTHES BRANDYWINE
Product Code
MNH
PMA / PMN Number
K992739
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO FDA WARNING LETTER DATED FEBRUARY 2012. DEVICE(S) LISTED IN THIS REPORT IS (ARE) USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. NO SAMPLE WAS RETURNED FOR EVALUATION. A REVIEW OF THE DEVICE HISTORY RECORD DID NOT SHOW CONDITIONS THAT COULD HAVE CONTRIBUTED TO THE REPORTED EVENT. THIS COMPLAINT IS CONSIDERED INVALID FROM A MANUFACTURING PERSPECTIVE.

Additional Manufacturer Narrative · 1

SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO FDA WARNING LETTER DATED FEBRUARY 2012. DEVICE(S) LISTED IN THIS REPORT IS (ARE) USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. ORIGINAL AWARENESS DATE IS 2/22/12.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A SCOLIOSIS REPAIR PROCEDURE, THREE COLLARS SNAPPED DURING TIGHTENING. THERE WERE BACK-UPS AVAILABLE THAT WERE USED. THE PATIENT WAS UNHARMED. THIS IS 2 OF 3 REPORTS FOR THE SAME EVENT.

Description of Event or Problem · 1

THIS IS REPORT 2 OF 3 FOR COMPLAINT (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
116173 TI COLLAR WITH GROOVES MNH SYNTHES BRANDYWINE 6847379

Patients

Seq Age Sex Outcome Treatment
1