MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-02-07 for PORTEX GENERAL ANESTHESIA CIRCUITS C37101307J manufactured by Smiths Medical Asd, Inc.
        [178215677]
Device evaluation in progress.
 Patient Sequence No: 1, Text Type: N, H10
        [178215678]
It was reported that during a pre-use check, the customer noticed that air was leaking from the anesthesia circuit. No patient injury or complications were reported in relation to this event.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3012307300-2019-06135 | 
| MDR Report Key | 9683501 | 
| Report Source | COMPANY REPRESENTATIVE,FOREIG | 
| Date Received | 2020-02-07 | 
| Date of Report | 2020-03-26 | 
| Date Mfgr Received | 2020-02-25 | 
| Device Manufacturer Date | 2019-08-16 | 
| Date Added to Maude | 2020-02-07 | 
| 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 55442 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 55442 | 
| Manufacturer G1 | SMITHS MEDICAL ASD, INC | 
| Manufacturer Street | 3350 GRANADA AVENUE NORTH SUITE 100 | 
| Manufacturer City | OAKDALE MN 55128 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 55128 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | PORTEX GENERAL ANESTHESIA CIRCUITS | 
| Generic Name | CIRCUIT, BREATHING (W CONNECTOR, ADAPTOR, Y PIECE) | 
| Product Code | CAI | 
| Date Received | 2020-02-07 | 
| Returned To Mfg | 2020-01-15 | 
| Catalog Number | C37101307J | 
| Lot Number | 3855885 | 
| Device Availability | R | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | Y | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | SMITHS MEDICAL ASD, INC | 
| Manufacturer Address | 6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2020-02-07 |