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By KathyBrownLaw, Jun 1 2017 09:44PM

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The FDA has issued a recall on select Zimmer Biomet fusion stimulators, due to “higher than allowed levels of potential harmful chemicals, which may be toxic to tissues and organs,” according to the FDA release.

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The recall affects approximately 33 select SpF Plus-Mini and SpF XL IIB implantable spinal fusion stimulators manufactured between Oct. 11, 2016 and Jan. 18, 2017 and distributed between March 28, 2017 and April 6, 2017.

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If you or someone you know has had one of these spinal implants, contact your physician immediately to find out if it is included in the recall.

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LINK:

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FDA labels Zimmer Biomet SpF Spinal Fusion Stimulator Recall as Class I

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