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Allergan Sales, LLC recalls Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,
Recalled May 8, 2024 · FDA recall Z-1694-2024 · Allergan Sales
Hazard
Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure. · FDA Class II
Units
10837
Sold at
US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.
Description
Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.
Product
Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,
Manufacturer(s)
Allergan Sales, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →