MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-13 for CARDINAL FLEXAL NITRILE EXAM GLOVES 88TN03M manufactured by Cardinal Health 200, Llc.
[138895074]
Exam gloves and dispensing box have metal flakes found on them.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5084895 |
MDR Report Key | 8420683 |
Date Received | 2019-03-13 |
Date of Report | 2019-03-04 |
Date of Event | 2019-02-24 |
Date Added to Maude | 2019-03-14 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
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 | 0 |
Brand Name | CARDINAL FLEXAL NITRILE EXAM GLOVES |
Generic Name | EXAM GLOVES POLYMER PATIENT EXAMINATION GLOVE |
Product Code | LZA |
Date Received | 2019-03-13 |
Returned To Mfg | 2019-02-25 |
Catalog Number | 88TN03M |
Lot Number | 3T18P035 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CARDINAL HEALTH 200, LLC |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-03-13 |