Procedure Products, Inc.: Medical Device Recalls in 2015

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Procedure Products, Inc. in 2015. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

U-SDN 2 Part Ultra Modified Seldinger Needles, NS/37-0387. All needles were sold in bulk, non-sterile, and intended for further processing. Needles are packaged in zipper-bags, 300 pieces per bag, with shipment occurring in a corrugated cardboard box. Needles consist of a stainless steel cannula with a molded plastic hub. This needle is intended to be placed over the guidewire to enlarge the opening in the vessel. Vessel dilator, for percutaneous catheterization.