| Subject: | Smith & Nephew Inc. Recalls 539 RF Denervation Probes |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 28 Mar 2007 - 12:00 am |
| Smith & Nephew Inc. has initiated a voluntary nationwide recall of 539 RF Denervation probes. The RF Denervation Probes, which are provided in a non-sterile condition, were mislabeled as sterile which potentially could result in a patient infection. According to Smith & Nephew Inc., the FDA has been apprised of this action. No injuries associated with this issue have been reported to date.
The Smith & Nephew RF Denervation probes are indicated for use exclusively with the Smith & Nephew... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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