MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2020-03-19 for PN 31X5 FRANCE 5B 325107 manufactured by Becton Dickinson And Co..
[186306899]
Date of event: unknown. The date received by manufacturer has been used for this field. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10
[186306900]
It was reported that an unspecified number of pn 31x5 france 5b experienced product damage/breakage with the device still considered operable. Product defect was noted prior to use. The following information was provided by the initial reporter: damaged products in a standard package.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9616656-2020-00242 |
MDR Report Key | 9856973 |
Report Source | DISTRIBUTOR,FOREIGN,OTHER |
Date Received | 2020-03-19 |
Date of Report | 2020-03-25 |
Date of Event | 2020-02-28 |
Date Mfgr Received | 2020-02-28 |
Device Manufacturer Date | 2018-05-23 |
Date Added to Maude | 2020-03-19 |
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 BRETT WILKO |
Manufacturer Street | 9450 SOUTH STATE STREET |
Manufacturer City | SANDY UT 84070 |
Manufacturer Country | US |
Manufacturer Postal | 84070 |
Manufacturer Phone | 8015652341 |
Manufacturer G1 | BECTON DICKINSON AND CO. |
Manufacturer Street | POTTERY ROAD |
Manufacturer City | DUN LAOGHAIRE CO |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PN 31X5 FRANCE 5B |
Generic Name | PEN NEEDLE |
Product Code | FMI |
Date Received | 2020-03-19 |
Catalog Number | 325107 |
Lot Number | 8143595 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON DICKINSON AND CO. |
Manufacturer Address | POTTERY ROAD DUN LAOGHAIRE CO |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-19 |