Ethicon Initiates Recall of Select Surgiflo Hemostatic Kits

Ethicon has initiated a recall of select Surgiflo hemostatic kits due to a packing issue, according to an FDA Safety Alert.

There is issue within the packing process where a cut could potentially breach the pouch of the packaging.

The recalled products (Surgiflo Hemostatic Matrix and Surgiflo Hemostatic Matrix Kit Plus FlexTip with Thrombin) were manufactured from Sept. 16, 2011 through July 27, 2012 and distributed from Sept. 29, 2011 through Aug. 7, 2012.

Ethicon sent an "Urgent Product Information" letter dated Aug. 21, 2012, to all affected customers. The letter identified the product, the problem and the action to be taken by the customer. Ethicon instructed customers to inspect their inventory to determine if they have any of the affected products.

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