Home › ADVANCED MEDICAL ASSOCIATES, LLC › Areza Medical
Areza Medical
ADVANCED MEDICAL ASSOCIATES, LLC · Model 44220 · UDI-DI 00850021481056
10
510(k) clearances
18,954
Adverse events (8 deaths)
19
Recalls
515
Facilities
Description
Areza Silicone Foam Dressing for Ostomies consists of a fenestrated, self-adhering, silicone wound contact layer, an absorbent polyurethane (PU) foam pad layer, and a vapor permeable and waterproof polyurethane film backing. The triple-layer construction facilitates dynamic fluid management to provide optimal moist wound environment; and may help reduce the risk of maceration. The absorbent pad layer provides superior absorption locking away exudates.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-29 | ConvaTec, Inc | Wound dressing may have foreign matter on the product. |
| 2025-02-19 | MEDLINE INDUSTRIES, LP - Northfield | There is a potential for the sterility of the device to be compromised. |
| 2022-01-28 | Sam Medical Products | Due to partially assembled valved dressing that has a hole within it instead of the intended non-valved dressing in the package resulting in that the dressing cannot be centered ov |
| 2021-08-20 | ConvaTec, Inc | Primary packaging labeling may be incorrect. |
| 2021-08-09 | ConvaTec, Inc | There is a potential for open seals which can compromise sterility. |
| 2018-08-01 | COVIDIEN LLC | Potential for product sterility breach due to a compromised or pinched seal defect |
| 2018-08-01 | COVIDIEN LLC | Potential for product sterility breach due to a compromised or pinched seal defect |
| 2018-08-01 | COVIDIEN LLC | Potential for product sterility breach due to a compromised or pinched seal defect |
| 2018-08-01 | COVIDIEN LLC | Potential for product sterility breach due to a compromised or pinched seal defect |
| 2018-08-01 | COVIDIEN LLC | Potential for product sterility breach due to a compromised or pinched seal defect |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.