MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-13 for MEDICAL ACTION INDUSTRIES 59391 manufactured by Medical Action Industries Inc..
[99908466]
Patient Sequence No: 1, Text Type: N, H10
[99908467]
Rust noted on tweezers after being used on patient wound.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 7266081 |
| MDR Report Key | 7266081 |
| Date Received | 2018-02-13 |
| Date of Report | 2018-02-07 |
| Date of Event | 2018-02-05 |
| Report Date | 2018-02-07 |
| Date Reported to FDA | 2018-02-07 |
| Date Reported to Mfgr | 2018-02-07 |
| Date Added to Maude | 2018-02-13 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MEDICAL ACTION INDUSTRIES |
| Generic Name | SUTURE REMOVAL KIT |
| Product Code | MCZ |
| Date Received | 2018-02-13 |
| Model Number | 59391 |
| Lot Number | 240899 |
| Operator | NURSE |
| Device Availability | Y |
| Device Age | 1 DY |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDICAL ACTION INDUSTRIES INC. |
| Manufacturer Address | 25 HEYWOOD RD ARDEN NC 28704 US 28704 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-02-13 |