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NEOFACE

Neoortho Produtos Ortopédicos S/A. · Model 925.103 · UDI-DI 07899893200689

DZL Prescription
1
510(k) clearances
1,522
Adverse events
8
Recalls
73
Facilities

Description

Self Tapping Screw SH Ø 2.4x 12 mm

Recalls

DateFirmReason
2016-02-23Synthes (USA) Products LLCOut of specification at the thread. The thread height of these screws is under-sized. The cross section of the affected area is less than that of conforming screws such that the th
2016-02-23Synthes (USA) Products LLCOut of specification at the thread. The thread height of these screws is under-sized. The cross section of the affected area is less than that of conforming screws such that the th
2013-05-31Synthes USA HQ, Inc.Synthes is initiating a voluntary Medical Device removal for specified part numbers and lot numbers of the Mutis Vector Distractor Pin Holding clamp, limited bone stock. The firm r
2013-01-11Synthes USA HQ, Inc.It was discovered that the sheer pin on the Multi-Vector Distractor may not be made according to product specifications.
2013-01-11Synthes USA HQ, Inc.It was discovered that the sheer pin on the Multi-Vector Distractor may not be made according to product specifications.
2013-01-11Synthes USA HQ, Inc.It was discovered that the sheer pin on the Multi-Vector Distractor may not be made according to product specifications.
2010-03-17Biomet Microfixation, Inc.Biomet Microfixation has received a complaint from a customer who reports finding a 3.5mm length screw in one 5 pack of 4mm length screws.
2009-10-06Biomet 3i, LLCBiomet 3i, Palm Beach Gardens, FL is recalling their Gold Slotted Retaining Screw 3MM, Model Number GS300. Product is Out Of Specification - product was manufactured with a materi

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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.