FDA Adverse Event Other Summary report: N

QUILL SRS

MDR report key: 1503782 · Received October 7, 2009

Report

Report Number
2522801-2009-00027
Event Type
Other
Date Received
October 7, 2009
Date of Event
September 1, 2009
Report Date
October 8, 2009
Manufacturer
SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)
Product Code
NEW
PMA / PMN Number
K051609
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE LOT NUMBER FOR THE PRODUCT USED BY THIS PHYSICIAN WAS NOT DISCLOSED. ONE OTHER ITEM WAS REPORTED BUT WAS NOT MENTIONED BY THE SURGEON AS ONE OF THE PRODUCTS THAT WAS USED FOR THIS SPECIFIC PROCEDURE. THERE WERE NO SAMPLES RETURNED FOR EVALUATION. METHOD: THE DEVICE WAS NOT RETURNED FOR EVALUATION. THE LOT NUMBERS WERE REPORTED AS UNKNOWN. FURTHERMORE, A REVIEW OF THE DEVICE HISTORY RECORD COULD NOT BE PERFORMED WITHOUT THE LOT CODE INFORMATION. RESULTS/CONCLUSION: THE DEVICE WAS NOT RETURNED FOR EVALUATION. NO PRODUCT EVALUATION CAN BE PERFORMED. (B)(4). RA-1065Q, QUILL SRS, #2 PDO, LOT# UNKNOWN. RA-1067Q, QUILL SRS, #0 PDO, LOT# UNKNOWN.

Description of Event or Problem · 1

THE DATE OF THE EVENT IS ESTIMATED: DR. (B)(6) PERFORMED A TOTAL HIP ARTHROPLASTY USING #2 QUILL FOR DEEP LAYER CLOSURE, 2-O VICRYL FOR INTERMEDIATE LAYER CLOSURE AND STAPLES AND DERMABOND FOR SKIN CLOSURE. SEVEN (7) DAYS POST OPERATIVE, THE PATIENT EXPERIENCED DEHISCENCE OF THE DEEP LAYER WHICH REQUIRED SURGICAL INTERVENTION TO REPAIR. PATIENT IS HEALING APPROPRIATELY WITH NO FURTHER INTERVENTION REQUIRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUILL SRS BARBED SUTURE WITH NEEDLE NEW SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH) RA-1065Q UNK

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention NONE MADE AVAILABLE.