MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2011-06-22 for CT 5M1546 manufactured by Nipro Corporation *usd*.
        [2071213]
This complaint originated as a result of a customer calling baxter to report a blood leak. The leak was at the beginning of treatment. The patient continued therapy with a different dialyzer, the patient went back on with a backup (b)(4) dialyzer and was okay. There was no patient injury and no medical intervention reported, the patient is doing fine.
 Patient Sequence No: 1, Text Type: D, B5
        [9155522]
(b)(4).
 Patient Sequence No: 1, Text Type: N, H10
| Report Number | 1423500-2011-08182 | 
| MDR Report Key | 2137233 | 
| Report Source | 05 | 
| Date Received | 2011-06-22 | 
| Date of Report | 2009-03-20 | 
| Date of Event | 2009-02-21 | 
| Date Mfgr Received | 2009-03-20 | 
| Date Added to Maude | 2012-02-13 | 
| 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 | KAREN KIRBY | 
| Manufacturer Street | 25212 W. ILLINOIS ROUTE 120 | 
| Manufacturer City | ROUND LAKE IL 60073 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 60073 | 
| Manufacturer Phone | 8472704541 | 
| Manufacturer G1 | NIPRO CORPORATION *USD* | 
| Manufacturer Street | 8-7 HANUKI-YACHI, NIIDA-AZA | 
| Manufacturer City | OHDATE-SHI | 
| Manufacturer Country | JA | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | CT | 
| Generic Name | HEMODIALYZER, RE-USE, HIGH FLUX | 
| Product Code | MSF | 
| Date Received | 2011-06-22 | 
| Catalog Number | 5M1546 | 
| Lot Number | 08J13CX | 
| Device Expiration Date | 2011-09-30 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Eval'ed by Mfgr | * | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | NIPRO CORPORATION *USD* | 
| Manufacturer Address | 8-7 HANUKI-YACHI, NIIDA-AZA OHDATE-SHI JA | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2011-06-22 |