← Search recalls
FDA (Device enforcement)Recalled 2024-12-16class ii

Integra LifeSciences Corp.: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides constant intraventricular pressure and drainage of CSF

Hazard

Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.

Details from the source

Reason for recall: Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels. Distribution: US Nationwide distribution in the states of FL, NC, MA, MN, OH, DC, VA, CA, WI, NE, TX, NY, MI, OR, NJ, SC, AZ, UT, RI, IN, GA, CO and the countries of Canada, Australia, New Zealand, Cyprus, Sweden, Finland, Slovenia and Great Britain. Quantity: 132 units Lot/code info: UDI-DI: 10381780535874. Lot Numbers: 7432470, 7434917, 7434918 and 7438322.

UPC codes

10381780535874

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify