MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-09-15 for CRAWFORD HOOK manufactured by Bausch And Lomb.
[26254539]
The tip of the crawford hook broke off during a procedure.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5056257 |
| MDR Report Key | 5088403 |
| Date Received | 2015-09-15 |
| Date of Report | 2015-09-15 |
| Date of Event | 2015-09-11 |
| Date Added to Maude | 2015-09-18 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | CRAWFORD HOOK |
| Generic Name | CRAWFORD HOOK |
| Product Code | HNQ |
| Date Received | 2015-09-15 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BAUSCH AND LOMB |
| Manufacturer Address | RANCHO CUCAMANGO CA 91730 US 91730 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2015-09-15 |