MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2018-09-20 for BENDING IRON - LEFT 2000-9046 manufactured by Zimmer Biomet Spine Inc..
[120900108]
Unique identifier (udi) #: ni. Current information is insufficient to permit a valid conclusion about the cause of this event. A follow up report will be sent upon completion of the device evaluation.
Patient Sequence No: 1, Text Type: N, H10
[120900109]
It was reported a torque wrench did not appear to be torquing correctly. During this same procedure, the tip of a rod bender chipped off while bending a rod. A different rod bender was used to complete the procedure. No patient harm was reported and no foreign bodies were retained. This is report two of two for this event.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3012447612-2018-00776 |
| MDR Report Key | 7893585 |
| Report Source | DISTRIBUTOR,HEALTH PROFESSION |
| Date Received | 2018-09-20 |
| Date of Report | 2019-01-21 |
| Date of Event | 2018-08-24 |
| Date Mfgr Received | 2019-01-16 |
| Device Manufacturer Date | 2008-10-21 |
| Date Added to Maude | 2018-09-20 |
| 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 | MS. ASHLEY MCPHERSON |
| 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 | BENDING IRON - LEFT |
| Generic Name | BENDER |
| Product Code | HXW |
| Date Received | 2018-09-20 |
| Returned To Mfg | 2018-09-07 |
| Model Number | NA |
| Catalog Number | 2000-9046 |
| Lot Number | 080610 |
| 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 | 2018-09-20 |