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Symmetry Kerrison

ASPEN SURGICAL PRODUCTS, INC. · Model 57-0904 · UDI-DI 00887482093948

HAE Prescription
1
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
63
Facilities

Description

Symmetry® Kerrison Rongeur; Thin Footplate; 90° Up; Micro; 4.0 mm; 9.0 mm Open; 9 in

Recalls

DateFirmReason
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.

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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.