MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2017-07-18 for ARGYLE 5558301726 manufactured by Covidien.
[80281805]
Submit date: 07/18/17. An investigation is currently under way; upon completion the results will be forwarded. A good faith effort will be made to obtain the applicable information relevant to the report. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[80281806]
The customer states the 7 mm suction tubing in the total knee pack is kinked and causing issue with the suction flow. The kink appears on one end and not the other end.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9612030-2017-05124 |
MDR Report Key | 6721048 |
Report Source | DISTRIBUTOR,FOREIGN |
Date Received | 2017-07-18 |
Date of Report | 2018-01-10 |
Date of Event | 2017-06-13 |
Date Mfgr Received | 2017-06-20 |
Date Added to Maude | 2017-07-18 |
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 | EDWARD ALMEIDA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5084524151 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | CALLE 9 SUR NO. 125 CUIDAD |
Manufacturer City | TIJUANA,NA 92173 |
Manufacturer Country | MX |
Manufacturer Postal Code | 92173 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARGYLE |
Generic Name | TUBING, NONINVASIVE |
Product Code | GAZ |
Date Received | 2017-07-18 |
Model Number | 5558301726 |
Catalog Number | 5558301726 |
Lot Number | 706515164X |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | CALLE 9 SUR NO. 125 CUIDAD TIJUANA,NA 92173 MX 92173 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-07-18 |