Synvasive Technology recalls
Synvasive Technology appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2020-04-15.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 4 |
|---|---|
| Published | 2013-04-24 to 2020-04-15 |
| By agency | FDA Device (4) |
| By classification | Class II (4) |
| By status | terminated (4) |
| Distribution named in notices | AL, CA, CT, MA, NY, US |
Recalls
- ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures
FDA Device · Class II · 2020-04-15 · Synvasive Technology
Reason: Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm. - Zimmer Oscillating Flat - TS ST Hub
FDA Device · Class II · 2015-12-30 · Synvasive Technology
Reason: Two lots of oscillating saw blades incorrectly identify the blade cutting width as 25mm instead of the correct specification of 19mm. - The Oxford Partial Knee
FDA Device · Class II · 2013-04-24 · Synvasive Technology
Reason: Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade. - Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc. (El Dorado Hills, CA) & manufactured under Synvasive Technolo…
FDA Device · Class II · 2013-04-24 · Synvasive Technology
Reason: Various reciprocating and oscillating saw blades were incorrectly labeled. The labeling errors include: (1) The pouch says oscillating saw blade when it actually contains a reciprocating saw blade; (2) The box bar code…