MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-30 for 2.7 MM COMPRESSION PLATE 6 HOLES 52 MM LENGTH NI 00492700600 manufactured by Zimmer Biomet, Inc..
[186555562]
(b)(4). Multiple mdr reports were filed for this event, please see associated reports: 0001822565 - 2020 - 01146, 0001822565 - 2020 - 01149, 0001822565 - 2020 - 01150, 0001822565 - 2020 - 01151, 0001822565 - 2020 - 01152, 0001822565 - 2020 - 01153, 0001822565 - 2020 - 01154, 0001822565 - 2020 - 01155, 0001822565 - 2020 - 01156, 0001822565 - 2020 - 01157, 0001822565 - 2020 - 01158, 0001822565 - 2020 - 01159, 0001822565 - 2020 - 01160, 0001822565 - 2020 - 01164, 0001822565 - 2020 - 01165, 0001822565 - 2020 - 01166, 0001822565 - 2020 - 01167, 0001822565 - 2020 - 01162, 0001822565 - 2020 - 01163, 0001822565 - 2020 - 01144. Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the product location is unknown. The investigation is in process. Once the investigation has been completed, a follow-up mdr will be submitted. If any further information which would change or alter any conclusions or information, a supplemental report will be filed accordingly. Zimmer biomet will continue to monitor for trends.
Patient Sequence No: 1, Text Type: N, H10
[186555563]
It was reported that patient underwent right orif distal tibia approximately 6 years ago. Subsequently, patient presented with pain over his right fibular plate that has gone on for years and is even so much that it wakes him up at night. Patient was revised approximately 1 month ago and all screws were removed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0001822565-2020-01145 |
| MDR Report Key | 9899445 |
| Report Source | HEALTH PROFESSIONAL,USER FACI |
| Date Received | 2020-03-30 |
| Date of Report | 2020-03-30 |
| Date of Event | 2020-02-26 |
| Date Mfgr Received | 2020-03-09 |
| Date Added to Maude | 2020-03-30 |
| 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 |
| Reporter Occupation | RISK MANAGER |
| 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 |
| Removal Correction Number | NI |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | 2.7 MM COMPRESSION PLATE 6 HOLES 52 MM LENGTH |
| Generic Name | PROSTHESIS, TRAUMA |
| Product Code | HRS |
| Date Received | 2020-03-30 |
| Model Number | NI |
| Catalog Number | 00492700600 |
| Lot Number | 403102914 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| 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 | 1. Hospitalization; 2. Required No Informationntervention | 2020-03-30 |