EBI Patient Care, Inc.: Medical Device Recalls in 2017

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by EBI Patient Care, Inc. in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

2017

10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels.
10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels.