MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-16 for PORTEX ANAESTHESIA BREATHING CIRCUIT, SINGLE-USE C45091795D-NL manufactured by Smiths Medical Asd, Inc..
[183476537]
Information was received that a smiths medical portex anaesthesia breathing circuit, single-use during procedures the bushing and the bag coming disconnected, no adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-02019 |
MDR Report Key | 9833531 |
Report Source | USER FACILITY |
Date Received | 2020-03-16 |
Date of Report | 2020-03-15 |
Date Mfgr Received | 2020-02-14 |
Date Added to Maude | 2020-03-16 |
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 | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE NORTH |
Manufacturer City | MINNEAPOLIS, MN |
Manufacturer Country | US |
Manufacturer G1 | SMITHS MEDICAL INTERNATIONAL LTD |
Manufacturer Street | BOUNDARY ROAD |
Manufacturer City | HYTHE, CT216JL |
Manufacturer Country | UK |
Manufacturer Postal Code | CT21 6JL |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PORTEX ANAESTHESIA BREATHING CIRCUIT, SINGLE-USE |
Generic Name | ANESTHESIA BREATHING CIRCUIT KIT (ADULT & PEDIATRIC) PRODUCT CODE: OFP |
Product Code | OFP |
Date Received | 2020-03-16 |
Returned To Mfg | 2020-02-28 |
Catalog Number | C45091795D-NL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD, INC. |
Manufacturer Address | 6000 NATHAN LANE NORTH MINNEAPOLIS, MN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-16 |