MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2018-06-27 for PITUITARY RONGEUR ? STRAIGHT ? 4MM 2856-14 manufactured by Zimmer Biomet Spine Inc..
[112559631]
Without a product return, no product evaluation is able to be conducted. Current information is insufficient to permit a valid conclusion about the cause of this event. If additional information is obtained that adds value to the relevant content of this report and/or a conclusion can be drawn, a follow-up report will be sent.
Patient Sequence No: 1, Text Type: N, H10
[112559632]
It was reported that the jaw on a rongeur was found to have broken after it went through post-operative cleaning. There were no patient impacts.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012447612-2018-00529 |
MDR Report Key | 7643019 |
Report Source | DISTRIBUTOR |
Date Received | 2018-06-27 |
Date of Report | 2018-10-26 |
Date of Event | 2018-05-29 |
Date Mfgr Received | 2018-10-23 |
Device Manufacturer Date | 2006-12-15 |
Date Added to Maude | 2018-06-27 |
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. GEOFFREY GANNON |
Manufacturer Street | 10225 WESTMOOR DR. NA |
Manufacturer City | WESTMINSTER CO 80021 |
Manufacturer Country | US |
Manufacturer Postal | 80021 |
Manufacturer Phone | 3034437500 |
Manufacturer G1 | ZIMMER BIOMET SPINE INC. |
Manufacturer Street | 10225 WESTMOOR DR. NA |
Manufacturer City | WESTMINSTER CO 80021 |
Manufacturer Country | US |
Manufacturer Postal Code | 80021 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PITUITARY RONGEUR ? STRAIGHT ? 4MM |
Generic Name | RONGEUR |
Product Code | HTX |
Date Received | 2018-06-27 |
Returned To Mfg | 2018-06-28 |
Model Number | NA |
Catalog Number | 2856-14 |
Lot Number | 42DG |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZIMMER BIOMET SPINE INC. |
Manufacturer Address | 10225 WESTMOOR DR. NA WESTMINSTER CO 80021 US 80021 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-06-27 |