Home / Brands / Synvasive Technology
Synvasive Technology Recalls
4 recalls on record · April 24, 2013 to April 15, 2020 · Medical Devices
Recalls by year
13
15
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 15, 2020Medical DevicesFDA
Synvasive Technology Inc recalls ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures.
Hazard: Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.
December 30, 2015Medical DevicesFDA
Synvasive Technology Inc recalls Zimmer Oscillating Flat - TS ST Hub; 75mm x 19mm x 1.00/1.27mm; Synvasive Part No. 11-4770: Part No. 19075127YT1;
Hazard: Two lots of oscillating saw blades incorrectly identify the blade cutting width as 25mm instead of the correct specification of 19mm.
April 24, 2013Medical DevicesFDA
Synvasive Technology Inc recalls The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, Syste
Hazard: Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
April 24, 2013Medical DevicesFDA
Synvasive Technology Inc recalls Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc. (El Dorado Hills, CA) & manufactured under
Hazard: 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 date does not match the human readable expiration date; and (3) The label incorrectly states use with Zimmer/Synthes handset and not the Zimmer Universal Power System.