MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2011-02-10 for ALUM CER LNR 32ID 56-66 71338456 manufactured by Smith & Nephew Orthopaedics, Inc..
[1729140]
It was reported that surgery time was extended due to breakage of the device.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1020279-2011-00034 |
MDR Report Key | 1983538 |
Report Source | 07 |
Date Received | 2011-02-10 |
Date of Report | 2011-02-10 |
Date of Event | 2010-12-21 |
Date Mfgr Received | 2011-01-11 |
Device Manufacturer Date | 2006-02-01 |
Date Added to Maude | 2011-02-10 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | CARLA SAMUELS |
Manufacturer Street | 1450 BROOKS ROAD |
Manufacturer City | MEMPHIS TN 38116 |
Manufacturer Country | US |
Manufacturer Postal | 38116 |
Manufacturer Phone | 9013995076 |
Manufacturer G1 | SMITH & NEPHEW ORTHOPAEDICS, INC. |
Manufacturer Street | 1450 BROOKS ROAD |
Manufacturer City | MEMPHIS TN 38116 |
Manufacturer Country | US |
Manufacturer Postal Code | 38116 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ALUM CER LNR 32ID 56-66 |
Generic Name | CERAMIC LINER |
Product Code | LPF |
Date Received | 2011-02-10 |
Model Number | 71338456 |
Catalog Number | 71338456 |
Lot Number | 06BM06912A |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW ORTHOPAEDICS, INC. |
Manufacturer Address | 1450 BROOKS ROAD MEMPHIS TN 38116 US 38116 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2011-02-10 |