FDAApril 20, 2017device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Zimmer Biomet is conducting a medical device field action for the SpF PLUS-Mini and SpF XL IIB Implantable Spinal Fusion Stimulator products due to higher than allowed cytotoxicity levels found during routine process monitoring with the product.

What to do

FDA enforcement status: Terminated

Brands named

ebi patient careebiebi patient

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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