FDA Adverse Event Injury Summary report: N

TEGADERM CHG DRESSING

MDR report key: 1873595 · Received October 12, 2010

Report

Report Number
2110898-2010-00111
Event Type
Injury
Date Received
October 12, 2010
Date of Event
August 12, 2010
Report Date
August 18, 2010
Manufacturer
3M HEALTH CARE
Product Code
FRO
PMA / PMN Number
K080620
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

DEVICE OR LOT CODE NOT PROVIDED TO MANUFACTURER FOR EVALUATION. COMPLAINT TYPE WILL BE MONITORED. THE INSERT PROVIDES THE FOLLOWING INFORMATION REGARDING OBSERVATION AND WHEN A DRESSING SHOULD BE CHANGED. SITE CARE: THE SITE SHOULD BE OBSERVED DAILY FOR SIGNS OF INFECTION OR OTHER COMPLICATIONS. IF INFECTION IS SUSPECTED, REMOVE THE DRESSING, INSPECT THE SITE DIRECTLY, AND DETERMINE APPROPRIATE MEDICAL INTERVENTION. INFECTION MAY BE SIGNALED BY FEVER, PAIN, REDNESS, SWELLING, OR UNUSUAL ODOR OR DISCHARGE. CHANGE THE DRESSING AS NECESSARY, IN ACCORDANCE WITH FACILITY PROTOCOL; DRESSING CHANGES SHOULD OCCUR AT LEAST EVERY 7 DAYS, PER CURRENT CDD RECOMMENDATIONS. DRESSING CHANGES MAY BE NEEDED MORE FREQUENTLY WITH HIGHLY EXUDATIVE SITES OR IF INTEGRITY OF THE DRESSING IS COMPROMISED.

Description of Event or Problem · 1

HEALTH CARE FACILITY REPORTED THAT A PT HAD DEVELOPED GREY, MUSHY SKIN AND PINK SATELLITES UNDER THE TEGADERM CHG PAD (AT THE IV SITE). THE CATHETER WAS REMOVED AND THE USE OF THE TEGADERM CHG WAS DISCONTINUED. THE OUTCOME OF THE SKIN CONDITION IS UNK. HOWEVER, NO FURTHER TREATMENT WAS NEEDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TEGADERM CHG DRESSING ANTIMICROBIAL IV SECUREMENT DRESSING FRO 3M HEALTH CARE NA KIT 10CB3608

Patients

Seq Age Sex Outcome Treatment
1 57 YR Required Intervention CATHETER SECURED WITH RETENTION SUTURES| PICC