TEGADERM CHG DRESSING
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
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.
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 |