FDA Adverse Event
Injury
Summary report: N
POLYSORB 2 36 UNDYED GS-13
MDR report key: 4006366
·
Received August 7, 2014
Report
- Report Number
- 1219930-2014-00637
- Event Type
- Injury
- Date Received
- August 7, 2014
- Date of Event
- June 27, 2014
- Report Date
- July 11, 2014
- Manufacturer
- COVIDIEN LP, FORMERLY US SURG
- Product Code
- GAN
- PMA / PMN Number
- K963253
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Description of Event or Problem · 1
PROCEDURE TYPE: NEUROMUSCULAR. ACCORDING TO THE REPORTER: THE CUSTOMER REPORTS THAT AFTER FITTING A PTG, THE "DEEP" SUTURE OF THE QUADRICEPS BROKE. THE PATIENT HAD TO BE RE-ADMITTED FOR SURGERY. (IT SEEMS LIKE THE THREAD RESORBS ITSELF PREMATURELY: THE SURGEON).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 462387 | POLYSORB 2 36 UNDYED GS-13 | POLYSORB | GAN | COVIDIEN LP, FORMERLY US SURG | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |