During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
Reason for recall: During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met. Distribution: US distribution to states of: IL and LA Quantity: 588 units Lot/code info: 1) MODEL/ITEM NUMBER AMAH40N: UDI/DI 00191072235473, Kit Lot Numbers: 42-7886011, 42-7990911; 2)MODEL/ITEM NUMBER CCKM67F: UDI/DI 00191072233578, Kit Lot Numbers: 70-053862, 70-053457, 70-053042, 70-052715, 70-052358, 70-051850, 70-051243; 3)MODEL/ITEM NUMBER HSTH03N: UDI/DI 00191072189615, Kit Lot Numbers: 42-7115711; 4)MODEL/ITEM NUMBER MIAH65B: UDI/DI 00191072235411, Kit Lot Numbers: 42-8134311; 5)MODEL/ITEM NUMBER MPWH01B: UDI/DI 00191072233271, Kit Lot Numbers: 5436801; 6)MODEL/ITEM NUMBER SPKA57T: UDI/DI 00191072235848, Kit Lot Numbers: 12-7400011, 12-7381311, 12-7358211, 12-7082111, 12-7157111, 12-7309911; 7)MODEL/ITEM NUMBER WVAH40H: UDI/DI 00191072233004, Kit Lot Numbers: 42-7897411, 42-7966211.
00191072235473, 00191072233578, 00191072189615, 00191072235411, 00191072233271, 00191072235848, 00191072233004
Official record: FDA (Device enforcement) ↗
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