Abbott Vascular recalls 20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)

Recalled April 20, 2022 · FDA recall Z-0921-2022 · Abbott Vascular

Hazard

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

Units

17 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 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)

Manufacturer(s)

Abbott Vascular

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