MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2018-01-03 for POOLE SUCTION INSTRUMENT 50/C 0035040 manufactured by Conmed Corporation.
[96506271]
The reported devices are expected to be returned for evaluation. A supplemental and final report will be filed upon the completion of the product evaluation and complaint investigation.
Patient Sequence No: 1, Text Type: N, H10
[96506272]
The distributor in (b)(4) rejected two poole suction instrument 50/c for "insufficient heatseal" during incoming inspection. In this instance, there was no patient involvement as the packaging anomaly was discovered during inspection prior to distribution to an end-user. The report is raised on the basis of a device malfunction with potential for injury with recurrence.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1320894-2017-00292 |
MDR Report Key | 7159678 |
Report Source | DISTRIBUTOR,FOREIGN,OTHER |
Date Received | 2018-01-03 |
Date of Report | 2018-02-14 |
Date Mfgr Received | 2018-02-13 |
Device Manufacturer Date | 2017-03-06 |
Date Added to Maude | 2018-01-03 |
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. LINDSEY SHEPPARD |
Manufacturer Street | 525 FRENCH ROAD |
Manufacturer City | UTICA NY 13502 |
Manufacturer Country | US |
Manufacturer Postal | 13502 |
Manufacturer Phone | 7273995209 |
Manufacturer G1 | CONMED CORPORATION |
Manufacturer Street | 525 FRENCH ROAD |
Manufacturer City | UTICA NY 13502 |
Manufacturer Country | US |
Manufacturer Postal Code | 13502 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | POOLE SUCTION INSTRUMENT 50/C |
Generic Name | SURGICAL INSTRUMENTS, STERILE |
Product Code | BYY |
Date Received | 2018-01-03 |
Returned To Mfg | 2018-02-05 |
Catalog Number | 0035040 |
Lot Number | 201703061 |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CONMED CORPORATION |
Manufacturer Address | 525 FRENCH ROAD UTICA NY 13502 US 13502 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-01-03 |