MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-01-22 for VAPRO HYDROPHILIC IC CH14 16 IN COUDE 73144 manufactured by Hollister Incorporated.
Report Number | 9616668-2020-00002 |
MDR Report Key | 9616253 |
Report Source | CONSUMER |
Date Received | 2020-01-22 |
Date of Report | 2020-01-22 |
Date of Event | 2019-12-30 |
Date Mfgr Received | 2019-12-30 |
Device Manufacturer Date | 2019-04-17 |
Date Added to Maude | 2020-01-22 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. LINDA WISOWATY |
Manufacturer Street | 2000 HOLLISTER DRIVE |
Manufacturer City | LIBERTYVILLE IL 600483781 |
Manufacturer Country | US |
Manufacturer Postal | 600483781 |
Manufacturer Phone | 8476802170 |
Manufacturer G1 | HOLLISTER ULC |
Manufacturer Street | FOXFORD RD. REHINS |
Manufacturer City | BALLINA, |
Manufacturer Country | EI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VAPRO HYDROPHILIC IC CH14 16 IN COUDE |
Generic Name | VAPRO HYDROPHILIC IC CH14 16 IN COUDE |
Product Code | GBM |
Date Received | 2020-01-22 |
Returned To Mfg | 2020-01-16 |
Catalog Number | 73144 |
Lot Number | 9C313 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HOLLISTER INCORPORATED |
Manufacturer Address | 2000 HOLLISTER DRIVE LIBERTYVILLE. 600483781 US 600483781 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-22 |