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 |