MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2017-10-16 for HIBBS OSTEOTOME 9-1/2 CVD 1/4 250160 manufactured by Integra York, Pa Inc..
[90469095]
To date the device involved in the reported incident has not been received for evaluation. An investigation has been initiated based on the reported information.
Patient Sequence No: 1, Text Type: N, H10
[90469096]
Fda sus voluntary event report mw5072083 reports that a small piece of osteotome that was used during procedure broke off in surgical site and was misplaced. X-ray was completed and the piece was located but unable to retrieve it.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2523190-2017-00113 |
| MDR Report Key | 6952310 |
| Report Source | USER FACILITY |
| Date Received | 2017-10-16 |
| Date of Report | 2017-10-06 |
| Date of Event | 2017-09-02 |
| Date Mfgr Received | 2017-10-23 |
| Device Manufacturer Date | 2015-03-02 |
| Date Added to Maude | 2017-10-16 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | USER SANDRA LEE |
| Manufacturer Street | 311 ENTERPRISE DRIVE |
| Manufacturer City | PLAINSBORO NJ 08536 |
| Manufacturer Country | US |
| Manufacturer Postal | 08536 |
| Manufacturer Phone | 6099362393 |
| Manufacturer G1 | INTEGRA YORK, PA INC. |
| Manufacturer Street | 589 DAVIES DRIVE |
| Manufacturer City | YORK PA 17402 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 17402 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HIBBS OSTEOTOME 9-1/2 CVD 1/4 |
| Generic Name | N/A |
| Product Code | GFI |
| Date Received | 2017-10-16 |
| Returned To Mfg | 2017-10-18 |
| Catalog Number | 250160 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | INTEGRA YORK, PA INC. |
| Manufacturer Address | 589 DAVIES DRIVE 589 DAVIES DRIVE YORK PA 17402 US 17402 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-10-16 |