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Acme Monaco Catheter Investigation Investigating a potential lawsuit on behalf of individuals who with catheter devices installed. Acme Monaco has recently recalled its .035×150 3MMJ TCFC guidewires, which are fitted inside catheters and used in surgical kits assembled and marketed by Medline Industries. The guidewires were recalled because there is a risk that the guidewire’s coating will flake off the wire, which the FDA has said could result in serious adverse health consequences. The recall has been classified as a “class 1” recall, which reflects a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. If you or someone you know has had a catheter installed that was manufactured by Acme Monaco, please contact us. |
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