MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2017-06-29 for 11G VERTEPORT CEMENT CANNULA (18/PKG) 0306511000 manufactured by Stryker Instruments-kalamazoo.
[78667059]
It was reported that the handle detached from the cannula during the end of the procedure. The cannula was successfully removed without the need for an incision. There was no clinically significant delay and no adverse consequences to the patient.
Patient Sequence No: 1, Text Type: D, B5
[115201769]
Patient Sequence No: 1, Text Type: N, H10
[115201770]
It was reported that the handle detached from the cannula during the end of the procedure. The cannula was successfully removed without the need for an incision. There was no clinically significant delay and no adverse consequences to the patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0001811755-2017-01350 |
MDR Report Key | 6676287 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2017-06-29 |
Date of Report | 2018-01-11 |
Date of Event | 2017-05-31 |
Date Mfgr Received | 2017-12-21 |
Date Added to Maude | 2017-06-29 |
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 | MR. ZACHARY BAKER |
Manufacturer Street | 4100 EAST MILHAM AVENUE |
Manufacturer City | KALAMAZOO MI 49001 |
Manufacturer Country | US |
Manufacturer Postal | 49001 |
Manufacturer Phone | 2693237700 |
Manufacturer G1 | STRYKER INSTRUMENTS-KALAMAZOO |
Manufacturer Street | 4100 EAST MILHAM AVENUE HIGHWAY #3, KM 130.2 |
Manufacturer City | KALAMAZOO MI 49001 |
Manufacturer Country | US |
Manufacturer Postal Code | 49001 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 11G VERTEPORT CEMENT CANNULA (18/PKG) |
Generic Name | CEMENT, BONE, VERTEBROPLASTY |
Product Code | OAR |
Date Received | 2017-06-29 |
Returned To Mfg | 2017-07-10 |
Catalog Number | 0306511000 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER INSTRUMENTS-KALAMAZOO |
Manufacturer Address | 4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-06-29 |