MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,other report with the FDA on 2019-02-12 for ILLINOIS (TJ) NEEDLE ASPIRATION 15GA TIN3015 manufactured by Carefusion, Inc.
[135932913]
(b)(4) initial emdr submission. A follow up emdr will be submitted if additional information is provided. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[135932914]
During the removal of this needle, the excessive resistance was felt, and then the patient? S tissue was damaged/scratched and needle? S tip deformed/bent.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1625685-2019-00008 |
| MDR Report Key | 8332538 |
| Report Source | DISTRIBUTOR,OTHER |
| Date Received | 2019-02-12 |
| Date of Report | 2019-02-27 |
| Date of Event | 2019-01-25 |
| Date Mfgr Received | 2019-01-25 |
| Date Added to Maude | 2019-02-12 |
| 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 | BDX ANNA WEHRHEIM |
| Manufacturer Street | 75 N. FAIRVIEW DRIVE |
| Manufacturer City | VERNON HILLS IL 60061 |
| Manufacturer Country | US |
| Manufacturer Postal | 60061 |
| Manufacturer G1 | CAREFUSION, INC |
| Manufacturer Street | 400 EAST FOSTER RD |
| Manufacturer City | MANNFORD OK 74044 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 74044 |
| Single Use | 3 |
| Remedial Action | OT |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ILLINOIS (TJ) NEEDLE ASPIRATION 15GA |
| Generic Name | BONE MARROW COLLECTION/TRANSFUSION KIT |
| Product Code | LWE |
| Date Received | 2019-02-12 |
| Catalog Number | TIN3015 |
| Lot Number | 0001142149 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION, INC |
| Manufacturer Address | 400 EAST FOSTER RD MANNFORD OK 74044 US 74044 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-02-12 |