MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2001-01-18 for SCRUB BRUSH W/12ML PCMX 4456A manufactured by Allegiance Healthcare Corp..
[202673]
Account states several nurses and techs had significant redness and irritation on forearms after scrubbing with this product. One tech took benadryl at the recommendation of a physician to clear it up.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1423507-2001-00017 |
MDR Report Key | 312987 |
Date Received | 2001-01-18 |
Date of Report | 2001-01-18 |
Date of Event | 2000-12-20 |
Date Facility Aware | 2000-12-21 |
Date Mfgr Received | 2000-12-21 |
Date Added to Maude | 2001-01-23 |
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 | 0 |
Manufacturer Contact | PATRICIA SHARPE-GREGG |
Manufacturer Street | 1500 WAUKEGAN ROAD |
Manufacturer City | MCGAW IL 60085 |
Manufacturer Country | US |
Manufacturer Postal | 60085 |
Manufacturer Phone | 8475783636 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SCRUB BRUSH W/12ML PCMX |
Generic Name | SCRUB BRUSH |
Product Code | GEC |
Date Received | 2001-01-18 |
Model Number | 4456A |
Catalog Number | 4456A |
Lot Number | YOPO852 |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | U |
Device Sequence No | 1 |
Device Event Key | 302737 |
Manufacturer | ALLEGIANCE HEALTHCARE CORP. |
Manufacturer Address | 1500 WAUKEGAN RD. MCGAW PARK IL 60085 US |
Baseline Brand Name | SCRUB BRUSH W/12ML PCMX |
Baseline Generic Name | SCRUB BRUSH |
Baseline Model No | 4456A |
Baseline Catalog No | 4456A |
Baseline ID | NA |
Baseline Device Family | SCRUB BRUSH |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K854232 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2001-01-18 |