device · product 1 of 1
Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,
- Recall number
- Z-1694-2024
- Initiated
- March 14, 2024
- Classification
- Class II
- Status
- Ongoing
- Recalling firm
- Allergan Sales, LLC
- Quantity
- 10837
App-derived interpretation
Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.
Official device-enrichment evidence · Sourced
Process design
Inspect official wording and provenance
Reason for recall
Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.
Code information
UDI: 10888628043725 / Lot #: 23B35C, 23B41C, 23B42C, 23C05C, 23C06C, 23D01C, 24C12C
Distribution pattern
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.