MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2011-10-19 for ION NITRIDED BLADE 0940023000 manufactured by Stryker Ireland Ltd..
[2292825]
It was reported that while cutting a padded cast from an ankle, the cast cutter blade broke. It was also reported that there was no pt or user injury and there was no delay to surgery.
Patient Sequence No: 1, Text Type: D, B5
[9385856]
The cast cutter blade associated with this event was returned to the mfr for eval. It was visually confirmed that the blade was broken. The returned blade was measured where possible and all critical specifications were met. Lot number info has not been provided to permit further investigation. The root cause is undetermined.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 9616696-2011-00196 |
MDR Report Key | 2321474 |
Report Source | 07 |
Date Received | 2011-10-19 |
Date of Report | 2011-09-22 |
Date of Event | 2011-09-21 |
Date Mfgr Received | 2011-09-22 |
Date Added to Maude | 2012-03-08 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | UNA BARRY |
Manufacturer Street | CARRIGTWOHILL BUSINESS & TECHNOLOGY PARK |
Manufacturer City | CARRIGTWOHILL, CO.CORK |
Manufacturer Country | EI |
Manufacturer Phone | 214532963 |
Manufacturer G1 | STRYKER IRELAND LTD. |
Manufacturer Street | CARRIGTWOHILL BUSINESS & TECHNOLOGY PARK |
Manufacturer City | CARRIGTWOHILL, CO.CORK |
Manufacturer Country | EI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ION NITRIDED BLADE |
Product Code | LGH |
Date Received | 2011-10-19 |
Returned To Mfg | 2011-10-07 |
Catalog Number | 0940023000 |
Lot Number | UNK |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER IRELAND LTD. |
Manufacturer Address | CARRIGTWOHILL, CO.CORK EI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2011-10-19 |