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Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc. Recalls

All product recalls associated with Synthes USA (HQ), Inc..

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Recall Summary

Total Recalls

104

Past Year

Class I (Serious)

Most Recent

Sep 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 81–100 of 104 recalls

Synthes USA (HQ), Inc.: SYNTHES TI MATRIXMANDIBLE SAGITTAL SPLIT PL 1.5MM THK/4H/...

The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification.

FDASep 3, 2009Nationwide• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: SYNTHES 2.0MM SCREW MANIPULATION FORCEPS, Catalog #SD397....

The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification.

FDASep 3, 2009Nationwide• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: SYNTHES BENDING PLIERS - STRAIGHT FOR CRANIOFACIAL/ORTHOG...

The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification.

FDASep 3, 2009

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Page 5 of 6Next

Nationwide

• Synthes USA (HQ), Inc.

Synthes USA (HQ), Inc.: SYNTHES TI MATRIXMANDIBLE SAGITTAL SPLIT PL 1.5MM THK/4H/...

The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification.

FDASep 3, 2009Nationwide• Synthes USA (HQ), Inc.

Synthes Spine: In Situ Bender Cutter Kit Wide Sterile, Catalog number 53...

Sterility may be compromised due to a ineffective package design.

FDAApr 3, 2009AL, AK, AZ +44 more• Synthes Spine

Synthes Spine: In Situ Bender Cutter Kit Narrow Sterile, Catalog number ...

Sterility may be compromised due to a ineffective package design.

FDAApr 3, 2009AL, AK, AZ +44 more• Synthes Spine

Synthes Spine: Synthes Zero-P StarDrive Screwdriver Shaft, T8, self-reta...

Tip breakage, due to inadequate instructions for use. The Technique Guide provided incorrect information related to use of the Torque Limiting Attachment during screw insertion and final tightening.

FDAFeb 10, 2009Nationwide• Synthes Spine