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Stryker Fecal Management System

SAGE PRODUCTS, LLC · Model 700-128 · UDI-DI 00618029980274

GDSEXB
2
510(k) clearances
1
Adverse events
3
Recalls
17
Facilities

Description

Stryker Fecal Management System

Recalls

DateFirmReason
2010-08-16BioMed LaboratoriesThe product may contain the mold Aspergillus ssp.
2010-08-16BioMed LaboratoriesThe product may contain the mold Aspergillus ssp.
2010-08-16BioMed LaboratoriesThe product may contain the mold Aspergillus ssp.

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Data 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.