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
| Date | Agency | Product | Recall number |
|---|---|---|---|
| February 13, 2013 | FDA | Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fus…Z-0781-2013 | Z-0781-2013 |
| November 21, 2012 | FDA | Synthes External Fixation System Tube to Tube Clamp, Part Number 390.007. Intended for…Z-0277-2013 | Z-0277-2013 |
| October 10, 2012 | FDA | MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS) for percutaneous…Z-0001-2013 | Z-0001-2013 |
| August 22, 2012 | FDA | Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001…Z-2206-2012 | Z-2206-2012 |
| August 1, 2012 | FDA | 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 REF 04.019.028S M…Z-2060-2012 | Z-2060-2012 |
| August 1, 2012 | FDA | 4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 REF 04.019.038S M…Z-2059-2012 | Z-2059-2012 |
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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