Spine Wave Recalls
2 recalls on record · September 18, 2013 to July 8, 2015 · Medical Devices
Recalls by year
13
15
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 8, 2015Medical DevicesFDA
Spine Wave, Inc. recalls Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and 10-1
Hazard: Mislabeled outer carton: Monopolar Probe is listed as 200 x 1.5mm when it should be listed as 280 x 1.5mm
September 18, 2013Medical DevicesFDA
Spine Wave, Inc. recalls StaXx¿ IB Convex Expandable Implant (25 x 12 x 9 mm), Intervertebral Fusion Device, Lumbar; Catalog Number 11 -1902.
Hazard: A component Superior endplate manufactured from a different polymer than specified