Synthes USA HQ, Inc.: 56 recalls on record

Recalls filed with 1 agency: FDA (56).

First recall on record: August 1, 2012. Most recent: January 8, 2014.

Risk classification: Class I: 1 · Class II: 55

Most recent recalls

DateAgencyProduct
November 6, 2013FDASynthes Application Instrument Sternal Zip Flex System intended for use in primary or …Z-0114-2014
October 23, 2013FDASynthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture, fixation, osteotomies,…Z-0014-2014
October 2, 2013FDASynthes Oracle Spacer System Slap Hammer, Part Number 03.809.690, Lot Number 3723847 T…Z-2282-2013
October 2, 2013FDASynthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 MM LCP Distal Humerus Syst…Z-2278-2013
September 25, 2013FDASynthes Cannulated Distal Femoral Nail (Trauma Nail), Part Number 450.851S, 420MM-Sterile…Z-2243-2013
September 4, 2013FDASynthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H HD/3H Shaft/Right Product Usage: Inte…Z-2087-2013
September 4, 2013FDASynthes Trauma Nail System. The devices are indication for bone fixation.Z-2058-2013
August 21, 2013FDASynthes Flexible Medullary Reamer. Intended to be used to facilitate the preparation o…Z-1952-2013
August 21, 2013FDA5.0mm Unit Rod 270mm 5.0mm Unit Rod 290mm 5.0mm Unit Rod 310mm 5.0mm Unit Rod 330mm 5…Z-1935-2013
August 7, 2013FDASynthes Synapse SD Drill Guide, Part Number SD389.477, Lot Number 6913900 Indicated fo…Z-1821-2013
August 7, 2013FDASynthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number 390.007,…Z-1816-2013
July 24, 2013FDASynthes CMF Distraction System The product is intended for use as a bone stabilizer an…Z-1726-2013
July 24, 2013FDAMulti Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is par…Z-1745-2013
June 26, 2013FDASynthes 11-Hole, 1/3 Tubular Plate DCL Plate with Collar, Part Number 241.000.011Z-1557-2013
May 15, 2013FDASynthes Radial Head Prosthesis: Trial Radial Head Elbow joint prosthesis: Synthes Radi…Z-1238-2013
April 17, 2013FDAFlexible Grip which is part of the Synthes Universal Nail System. Indicated for the co…Z-1062-2013
April 3, 2013FDASynthes Dens Instrument Set (Dens Graphic Case), Part Number 687.030 (also known as the A…Z-1016-2013
March 27, 2013FDAVariable Angle Locking Compression Plate/VA-LCP Dorsal Distal Radius Plate, Part Number 0…Z-0956-2013
March 20, 2013FDALarge Combination Clamp/Large External Fixation System, Part Number 390.005 Product Us…Z-0941-2013
March 20, 2013FDASynthes Titanium Midface Distractor, MR Conditional, Part number 487.982. For temporary …Z-0942-2013
March 20, 2013FDASynthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Core 40 mm Thread Length, Part …Z-0938-2013
March 13, 2013FDASynthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left), Part Number 487…Z-0905-2013
March 13, 2013FDASynthes Multi-Vector Distractor Body, Part Number 487.931. For mandibular bone lengthe…Z-0903-2013
March 13, 2013FDASynthes Multi-Vector Distractor, Multi-axial Mandible Distractor (Right), Part Number 487…Z-0904-2013
February 13, 2013FDASynthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fus…Z-0782-2013

Questions about this company

How many recalls does Synthes USA HQ, Inc. have?
Recalert has 56 U.S. recalls on record for Synthes USA HQ, Inc., published between August 1, 2012 and January 8, 2014.
Which agencies have handled Synthes USA HQ, Inc. recalls?
Synthes USA HQ, Inc. appears as the recalling firm in recalls from: FDA (56).

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