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

Recall date

March 11, 2022

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0921-2022

FDA classification

Class II

Brand / firm

Abbott Vascular

Sold / distributed

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, Austral…

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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