SpineFrontier Recalls
33 recalls on record · November 28, 2012 to July 24, 2019 · Medical Devices
Recalls by year
12
13
14
15
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 12, 2013Medical DevicesFDA
SpineFrontier, Inc. recalls Straight Impactor - Dorado IBC, Part Number: SI02140. The device is used to position implants after they have been inser
Hazard: During two separate occasions an impactor plate on the handle broke off while being struck by a mallet.
November 28, 2012Medical DevicesFDA
SpineFrontier, Inc. recalls S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: 11-50223 Product Usage: Surgical Guides allow
Hazard: When using the optional S-LIFT (also known as S-LIF) Implant Guides without stops, there is a known risk of moving the Implant Guides, and possibly the implant, too far into the disc space creating the potential for injury to the patient. The instructions for Use for the S-Lift Implant Guides will be amended to add the following warning: "Care is to be taken to not over insert the Implant Guides
November 28, 2012Medical DevicesFDA
SpineFrontier, Inc. recalls Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide pressure to drive spikes of Insp
Hazard: Inspan Compressors may break at weld causing a loss of compression