SEPRAFILM (SODIUM HYALURONATE, CARBOXYMETHYLCELLULOSE) MEMBRANE
Report
- Report Number
- 1220423-2011-00032
- Event Type
- Other
- Date Received
- August 10, 2011
- Report Date
- August 4, 2011
- Manufacturer
- GENZYME BIOSURGERY (SEPRAFILM/PACK)
- Product Code
- MCN
- PMA / PMN Number
- P950034
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
MFR'S COMMENT: THE BENEFIT-RISK RELATIONSHIP OF SEPRAFILM IS NOT AFFECTED BY THIS REPORT. (B)(4).
SUBCUTANEOUS ABSCESS (SLURRY) [SUBCUTANEOUS ABSCESS]. CASE DESCRIPTION: LITERATURE-TRIAL REPORT WAS RECEIVED ON (B)(4) 2011, FROM A PHYSICIAN REGARDING A PT (IDENTIFIERS NOT PROVIDED). THIS REPORT IS FROM A LITERATURE ARTICLE ENTITLED "SEPRAFILM SLURRY DOES NOT INCREASE COMPLICATION RATES AFTER LAPAROSCOPIC COLECTOMY". THERE WERE TWO GROUPS. GROUP 2 CONSISTED OF 50 PTS WHO UNDERWENT LAPAROSCOPIC COLECTOMY FOLLOWED BY THE APPLICATION OF THE SEPRAFILM SLURRY. THE SLURRY WAS CREATED AT THE END OF THE OPERATION BY DISSOLVING TWO PROCEDURE PACKS (EACH CONTAINING SIX 3X6 INCH SHEETS) OF SEPRAFILM IN 120 ML OF WARM NORMAL SALINE. THE SLURRY WAS DELIVERED INTO THE PERITONEAL CAVITY USING A 16-FR. ROBINSON CATHETER. ONE PT EXPERIENCED A SUBCUTANEOUS ABSCESS WHICH WAS MANAGED BY PERCUTANEOUS DRAINAGE AND ANTIBIOTICS. THE ACTION TAKEN WITH SEPRAFILM WAS NOT PROVIDED. THE PT'S OUTCOME WAS NOT PROVIDED. CONCOMITANT MEDICATIONS WERE NOT PROVIDED. THE RELATIONSHIP BETWEEN SEPRAFILM AND THE EVENT OF SUBCUTANEOUS ABSCESS WAS NOT PROVIDED BY THE REPORTING PHYSICIAN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SEPRAFILM (SODIUM HYALURONATE, CARBOXYMETHYLCELLULOSE) MEMBRANE | BIORESORBABLE ADHESION BARRIER | MCN | GENZYME BIOSURGERY (SEPRAFILM/PACK) | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | Required Intervention |