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STRYKER CORPORATION · Model 0298097100S1 · UDI-DI 07613153089674

DWH Prescription
4
510(k) clearances
159
Adverse events (1 deaths)
1
Recalls
35
Facilities

Description

Sternum Blade (31.1 x 0.79mm), Non-Sterile

Recalls

DateFirmReason
2011-11-17Terumo Cardiovascular Systems CorporationTerumo Cardiovascular Systems has received one report of minute metal shavings leaking from the Sarns Sternal Saw I System at the point where the saw blade is inserted into the saw

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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.