MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-08-13 for ANCHORFAST ORAL ENDOTRACH TUBE FASTENER 9799 manufactured by Hollister Incorporated.
Report Number | 1119193-2019-00032 |
MDR Report Key | 8888585 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-08-13 |
Date of Report | 2019-08-13 |
Date of Event | 2019-07-08 |
Date Mfgr Received | 2019-07-29 |
Date Added to Maude | 2019-08-13 |
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 | 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 INCORPORATED |
Manufacturer Street | 366 DRAFT AVENUE |
Manufacturer City | STUARTS DRAFT VA 244779998 |
Manufacturer Country | US |
Manufacturer Postal Code | 244779998 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ANCHORFAST ORAL ENDOTRACH TUBE FASTENER |
Generic Name | ANCHORFAST ORAL ENDOTRACH TUBE FASTENER |
Product Code | CBH |
Date Received | 2019-08-13 |
Returned To Mfg | 2019-08-07 |
Catalog Number | 9799 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
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 | 2019-08-13 |