MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-03-05 for LOCK SCREW SQUARE 131227126 manufactured by Zimmer Biomet, Inc..
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(b)(4). (b)(6). If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly. Zimmer biomet will continue to monitor for trends.
Patient Sequence No: 1, Text Type: N, H10
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It was reported that during in house inspection, hair was found inside the packaging. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0001825034-2019-00961 |
| MDR Report Key | 8391984 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2019-03-05 |
| Date of Report | 2019-08-23 |
| Date Mfgr Received | 2019-08-19 |
| Device Manufacturer Date | 2017-06-12 |
| Date Added to Maude | 2019-03-05 |
| 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. CHRISTINA ARNT |
| Manufacturer Street | 56 E. BELL DR. |
| Manufacturer City | WARSAW IN 46582 |
| Manufacturer Country | US |
| Manufacturer Postal | 46582 |
| Manufacturer Phone | 5745273773 |
| Manufacturer G1 | ZIMMER BIOMET, INC. |
| Manufacturer Street | 56 E. BELL DRIVE |
| Manufacturer City | WARSAW IN 46582 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 46582 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LOCK SCREW SQUARE |
| Generic Name | APPLIANCE, FIXATION |
| Product Code | LXT |
| Date Received | 2019-03-05 |
| Returned To Mfg | 2019-02-26 |
| Catalog Number | 131227126 |
| Lot Number | SBM079690 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ZIMMER BIOMET, INC. |
| Manufacturer Address | 56 E. BELL DRIVE WARSAW IN 46582 US 46582 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-03-05 |