MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2019-12-23 for FEMORAL TEMPLATE STD LM/RL SIZE 1 160141 manufactured by Mako Surgical Corp..
[175876261]
As part of the normal complaint follow-up, an evaluation of the event has been initiated by mako surgical. A supplemental report will be submitted when additional information becomes available.
Patient Sequence No: 1, Text Type: N, H10
[175876262]
As reported by a mako product manager: "if we are not wrong, we noticed a mistake of translation for the mako restoris size 1 femoral trial ref 160141... In english it? S lm/rl while the translation in french means internal right/external left. "a. Pdf supplied of the label appears to be a sample label, not a packaging label. It is unknown if any physical labels/ devices are involved at this time.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3005985723-2019-00918 |
MDR Report Key | 9513167 |
Report Source | COMPANY REPRESENTATIVE,OTHER |
Date Received | 2019-12-23 |
Date of Report | 2020-03-13 |
Date of Event | 2019-11-26 |
Date Mfgr Received | 2020-02-14 |
Date Added to Maude | 2019-12-23 |
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. COLLIN NEITZEL |
Manufacturer Street | 325 CORPORATE DRIVE |
Manufacturer City | MAHWAH NJ 07430 |
Manufacturer Country | US |
Manufacturer Postal | 07430 |
Manufacturer Phone | 2018315000 |
Manufacturer G1 | MAKO SURGICAL CORP. |
Manufacturer Street | 2555 DAVIE ROAD |
Manufacturer City | FORT LAUDERDALE FL 33317 |
Manufacturer Country | US |
Manufacturer Postal Code | 33317 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FEMORAL TEMPLATE STD LM/RL SIZE 1 |
Generic Name | PROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAINED, CEMENTED, POLYM |
Product Code | NPJ |
Date Received | 2019-12-23 |
Model Number | 160141 |
Catalog Number | 160141 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MAKO SURGICAL CORP. |
Manufacturer Address | 2555 DAVIE ROAD FORT LAUDERDALE FL 33317 US 33317 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-12-23 |