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STERILMED, INC. · Model SCI04526-01 · UDI-DI 10888551040372

NKU Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
0
Facilities

Description

BALLOON INFLATION DEVICE ENCORE 26

Recalls

DateFirmReason
2008-08-08Sterilmed IncSteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility e

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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.