Abbott Vascular recalls 20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)

Recalled April 20, 2022 · FDA recall Z-0923-2022 · Abbott Vascular

Hazard

Due to an increase in complaint trend for leaks and intermittent/loose connections. · FDA Class II

Units

131 lots

Sold at

U.S Nationwide Distribution.: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, SC, TN, TX, VA, WA, and WI. O.U.S.: United Arab Emirates, France, Pakistan, Argentina, United Kingdom, Portugal, Australia, Greece, R¿union, Belgium, Guam, Romania, Brazil, Indonesia, Russian Federation, Bahamas, Israel, Saudi Arabia, Canada, India, Singapore, Switzerland, Italy, Slovakia, Chile, Jamaica, Thailand, China, Japan, Taiwan Republic of China, Colombia, Korea (South), Costa Rica, Luxembourg, Uruguay, Czech Republic, Mexico, Vietnam, Germany, Netherlands, South Africa, Dominican Republic, New Zealand, Spain, and Panama

Description

Due to an increase in complaint trend for leaks and intermittent/loose connections.

Product

20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)

Manufacturer(s)

Abbott Vascular

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →