MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01 report with the FDA on 2011-06-23 for HAKIM VENTRICULAR & PERITONEAL CATHETERS WITH BACTISEAL 82-3072 manufactured by Codman & Shurtleff, Inc Medos S.a..
[18202538]
It has been communicated that the device and/or lot information is not available for evaluation. Without the device and/or lot information it is not possible for codman to conduct a proper investigation. If at some point the device and/or lot information does become available, this complaint will be re-opened, evaluated and a follow up report will be filed. Trends will be monitored for this and similar complaints. At the present time this complaint is considered closed.
Patient Sequence No: 1, Text Type: N, H10
[18377204]
Surgeon reported that pt was unwell and developed a fever and it was difficult to ascertain a cause.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1226348-2011-00228 |
MDR Report Key | 2143038 |
Report Source | 01 |
Date Received | 2011-06-23 |
Date Mfgr Received | 2011-05-25 |
Date Added to Maude | 2011-06-30 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | MATTHEW KING |
Manufacturer Street | 325 PARAMOUNT DR. |
Manufacturer City | RAYNHAM MA 02767 |
Manufacturer Country | US |
Manufacturer Postal | 02767 |
Manufacturer Phone | 5088283106 |
Manufacturer G1 | CODMAN & SHURTLEFF, INC. |
Manufacturer Street | RUE GIRARDET 29 |
Manufacturer City | LE LOCLE CH-2400 |
Manufacturer Country | SZ |
Manufacturer Postal Code | CH-2400 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HAKIM VENTRICULAR & PERITONEAL CATHETERS WITH BACTISEAL |
Generic Name | SHUNT, CENTRAL NERVOUS SYSTEM & COMPS |
Product Code | HCA |
Date Received | 2011-06-23 |
Model Number | NA |
Catalog Number | 82-3072 |
Lot Number | UNK |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CODMAN & SHURTLEFF, INC MEDOS S.A. |
Manufacturer Address | RUE GIRARDET 29 LE LOCLE CH-2400 SZ CH-2400 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2011-06-23 |