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LAZIC

Peter Lazic GmbH · Model 70.093.03 B · UDI-DI 04250603740469

HYA Prescription
0
510(k) clearances
11
Adverse events (1 deaths)
1
Recalls
106
Facilities

Description

L-LINE CLASSIC MICRO NEEDLE HOLDER BAYONET JAWS:0,5 MMUPWARDS CURVED, 205MM 8 1/8" WORKING END YASARGIL,BLACK COATED

Recalls

DateFirmReason
2015-06-17Biomet, Inc.Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone.

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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.