A recall initiated by Zimmer Biomet involving 33 select SpF Plus-Mini and SpF XL IIB implantable spinal fusion stimulators has been classified by the FDA as Class I. The recall was issued over concerns about higher-than-permitted levels of chemicals that could be harmful to organs and tissues, posing risks of serious adverse health consequences.
Recall of Zimmer Biomet's spinal fusion stimulators labeled as Class I by FDA
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