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
January 8, 2014FDASynthes Hand Switch - Electric Pen Drive, Part Number 05.001.012 The Synthes Electric …Z-0615-2014
December 18, 2013FDASynthes Trochanteric Fixation Nail As part of the Synthes Trochanteric Fixation Nail …Z-0474-2014
December 18, 2013FDASynthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is used for open a…Z-0473-2014
December 11, 2013FDATitanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and unstable …Z-0452-2014
December 11, 2013FDASynthes Soft Tissue Retractor Small Extendible. Offset blade facilitates easy preparat…Z-0429-2014
December 11, 2013FDASynthes Zero-P VA Implant 7 MM Height Parallel Sterile The Synthes Zero-P VA Implant 7…Z-0455-2014
December 4, 2013FDAVertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement i…Z-0410-2014
December 4, 2013FDASynthes Material Mix (Adjustable Cervical Distractor-Right, Matrix Distractor Rack, T-PAL…Z-0393-2014
December 4, 2013FDASynthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER Synthes 4.5MM TI VA-LCP CRV…Z-0401-2014
December 4, 2013FDASynthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: The Matrix 5.5.mm…Z-0391-2014
December 4, 2013FDASynthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar pedical s…Z-0384-2014
December 4, 2013FDASynthes Tensioning Device The Synthes Osteogenesis System, MR Conditional is intended…Z-0388-2014
December 4, 2013FDALarge Buttress Compression Nut For Blade Guide Sleeve TFN The Synthes Large Buttress …Z-0387-2014
December 4, 2013FDASynthes Titanium Cannulated Humeral Nail Intended to aid in the alignment and stabili…Z-0407-2014
December 4, 2013FDASynthes Titanium Minimally Invasive Reduction Screw System Locking Cap, Part Number 04.63…Z-0396-2014
December 4, 2013FDASynthes Spiked Washers 13.5/6.5 Spiked Washers 13.5/6.5 are intended to be used in lig…Z-0394-2014
December 4, 2013FDASlipped Capital Femoral Epiphysis System Product Usage: Intended for fracture fixati…Z-0408-2014
December 4, 2013FDASynthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder for Synfix (TM)-L…Z-0405-2014
December 4, 2013FDASynthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary di…Z-0409-2014
December 4, 2013FDA3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm and 5.0mm Dynamic …Z-0390-2014
December 4, 2013FDA2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recess 12 MM Fixation of fractur…Z-0380-2014
December 4, 2013FDASynthes Titanium Minimally Invasive Reduction Screw System Polyaxial Screw Body, Part Num…Z-0395-2014
November 27, 2013FDASynthes Soft Tissue Retractor Small Extendible Offset blade facilitates easy preparati…Z-0341-2014
November 27, 2013FDASynthes Titanium Trochanteric Fixation Nail (TFN)-Helical Blade Synthes Titanium Troch…Z-0369-2014
November 20, 2013FDASynthes 8.5 MM Medullary Reamer Product Usage: An orthopedic manual surgical instrum…Z-0202-2014

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.
What was the most recent Synthes USA HQ, Inc. recall?
FDA recall Z-0615-2014, published January 8, 2014: Synthes Hand Switch - Electric Pen Drive, Part Number 05.001.012 The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, dec…
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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