MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2020-01-03 for CAPTURE-R READY INDICATOR CELL 0006428 manufactured by Immucor, Inc..
Report Number | 1034569-2020-00001 |
MDR Report Key | 9548822 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2020-01-03 |
Date of Report | 2020-01-03 |
Date of Event | 2019-12-11 |
Date Mfgr Received | 2019-12-13 |
Date Added to Maude | 2020-01-03 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR HOWARD YOREK |
Manufacturer Street | 3130 GATEWAY DRIVE |
Manufacturer City | NORCROSS GA 300915625 |
Manufacturer Country | US |
Manufacturer Postal | 300915625 |
Manufacturer Phone | 7704412051 |
Manufacturer G1 | IMMUCOR, INC. |
Manufacturer Street | 3130 GATEWAY DRIVE |
Manufacturer City | NORCROSS GA 300915625 |
Manufacturer Country | US |
Manufacturer Postal Code | 300915625 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CAPTURE-R READY INDICATOR CELL |
Generic Name | QUALITY CONTROL KIT FOR BLOOD BANKING REAGENTS |
Product Code | KSF |
Date Received | 2020-01-03 |
Catalog Number | 0006428 |
Lot Number | 221442 |
Device Expiration Date | 2019-12-15 |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | IMMUCOR, INC. |
Manufacturer Address | 3130 GATEWAY DRIVE NORCROSS GA 300915625 US 300915625 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-03 |