FDA Adverse Event
Malfunction
Summary report: N
1.1MM TW DRILL FOR 1.50MM SCR
MDR report key: 3240376
·
Received July 17, 2013
Report
- Report Number
- 1045834-2013-03356
- Event Type
- Malfunction
- Date Received
- July 17, 2013
- Date of Event
- June 1, 2013
- Report Date
- June 17, 2013
- Manufacturer
- DEPUY SYNTHES POWER TOOLS
- Product Code
- HBC
- PMA / PMN Number
- K011444
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SZ
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE ACTUAL DEVICE WAS RETURNED FOR EVAL. RELIABILITY ENGINEERING EVALUATED THE DEVICE AND OBSERVED IF ADD'L INFO SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SENT ACCORDINGLY.
Description of Event or Problem · 1
IT WAS REPORTED FROM (B)(6) THAT DURING INCOMING INSPECTION, IT WAS OBSERVED THAT THERE WAS "RESIDUE IN THE STERILE PACKAGE" OF THE DEVICE. THE DEVICE WAS NOT USED IN SURGERY. NO INJURIES OF MEDICAL INTERVENTION WERE REPORTED. THE EXACT DATE OF THE EVENT WAS UNK. ALTHOUGH THE REPORTER CLARIFIED THE EVENT OCCURRED IN (B)(6) 2013. ALL AVAILABLE INFO HAS BEE DISCLOSED. IF ADD'L INFO SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SUBMITTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 331175 | 1.1MM TW DRILL FOR 1.50MM SCR | HBC | DEPUY SYNTHES POWER TOOLS | F493072383 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |