TI RIB HOOK
Report
- Report Number
- 2530088-2013-00229
- Event Type
- Injury
- Date Received
- February 28, 2013
- Date of Event
- January 31, 2013
- Report Date
- January 31, 2013
- Manufacturer
- SYNTHES BRANDYWINE
- Product Code
- MDI
- PMA / PMN Number
- H03009
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UT
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
DEVICE IS USED FOR TREATMENT, NOT DIAGNOSIS. DATE OF EVENT - (B)(6) 2013, PROVIDED BY QUESTIONNAIRE ON (B)(6) 2013. DATE ILLEGIBLE AND CONFIRMED BY TELEPHONE ON (B)(6) 2013. PLACEHOLDER.
DEVICE USED FOR TREATMENT AND NOT DIAGNOSIS. WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED.
THIS IS 3 OF 4 REPORTS FOR COMPLAINT (B)(4).
A VEPTR REPLACEMENT OF A RIB HOOK DUE TO MIGRATION: PATIENT WAS IMPLANTED WITH VEPTR ON AN UNKNOWN DATE. ON A FOLLOW UP VISIT TO SURGEON AN X-RAY REVEALED THE MIGRATION. THE SALES CONSULTANT DOES NOT KNOW IF THE PATIENT WAS HAVING PAIN AS HE IS A (B)(6) MALE WITH SPINA BIFIDA AND NON VERBAL. WHEN THE SURGEON WAS ATTEMPTING TO MOVE THE HOOK TO ANOTHER RIB WITH THE FORCEPS, THE FORCEPS BROKE IN HALF. THE PIECES WERE RETRIEVED AND THE SURGEON USED THE SECOND INSTRUMENT IN THE SET WITHOUT DELAY TO THE CASE. IT WAS NOTED BY THE CONSULTANT: IT DID NOT APPEAR AS IF THE SURGEON WAS PUTTING THAT MUCH FORCE ON THE INSTRUMENT. NO ADVERSE EFFECT TO THE PATIENT WAS NOTED. THE HOOK WAS MOVED FROM THE 3RD TO THE 4TH RIB. THIS IS 3 OF 4 REPORTS FOR THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 86700 | TI RIB HOOK | RIB HOOK | MDI | SYNTHES BRANDYWINE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 15 YR | Required Intervention |