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AESCULAP

Aesculap AG · Model OG129R · UDI-DI 04046964073137

JYO Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Round Cutting Knife, 0 °, straight, 6 1/4" (160 mm), diam. 3 mm

Recalls

Date	Firm	Reason
2013-03-27	Summit Medical, Inc.	Summit Medical has initiated a recall of Myringotomy Lance Blade (Juvenile) because the box contains the wrong blade. The box contains Myringotomy Spear Blade (Juvenile).

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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.