MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1999-08-24 for SHOE COVER, GRIPPER * NON23758 manufactured by Medline Industries, Inc..
[19958611]
Reportedly, personnel have slipped while wearing shoe covers, one nurse broke a finger and required stitches.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1417592-1999-00024 |
MDR Report Key | 237138 |
Report Source | 06 |
Date Received | 1999-08-24 |
Date of Report | 1999-07-21 |
Date of Event | 1999-07-19 |
Date Reported to FDA | 1999-10-15 |
Date Reported to Mfgr | 1999-10-15 |
Date Added to Maude | 1999-08-27 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | LARA SIMMONS |
Manufacturer Street | ONE MEDLINE PLACE |
Manufacturer City | MUNDELEIN IL 60060 |
Manufacturer Country | US |
Manufacturer Postal | 60060 |
Manufacturer Phone | 8479492639 |
Manufacturer G1 | MEDLINE INDUSTRIES, INC. |
Manufacturer Street | ONE MEDLINE PLACE |
Manufacturer City | MUNDELEIN IL 60060 |
Manufacturer Country | US |
Manufacturer Postal Code | 60060 |
Single Use | 3 |
Remedial Action | RC |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SHOE COVER, GRIPPER |
Generic Name | SHOE COVER |
Product Code | FXP |
Date Received | 1999-08-24 |
Model Number | * |
Catalog Number | NON23758 |
Lot Number | 9393372JC1 |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 229807 |
Manufacturer | MEDLINE INDUSTRIES, INC. |
Manufacturer Address | ONE MEDLINE PLACE MUNDELEIN IL 60060 US |
Baseline Brand Name | SHOE COVER, GRIPPER, NON-SKID |
Baseline Generic Name | SHOE COVER |
Baseline Model No | NON23758 |
Baseline Device Family | DI01 |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 1999-08-24 |