Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
Reason for recall: Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker. Distribution: US Nationwide distribution. Quantity: 25877 units Lot/code info: 1) REF CDS983478L, UDI/DI 10195327497286 (each) 40195327497287 (case), Lot Numbers: 23JDA999, 23KDB756, 24ADA957, 24DDA553; 2) REF CDS983478M, UDI/DI 10198459000065 (each) 40198459000066 (case), Lot Numbers: 24EDB504; 3) REF CDS983493M, UDI/DI 10195327497415 (each) 40195327497416 (case), Lot Numbers: 23LDA144, 24ADA328; 4) REF CDS983496L, UDI/DI 10195327497408 (each) 40195327497409 (case), Lot Numbers: 23KDC085, 24ADB601; 5) REF CDS983496M, UDI/DI 10198459000201 (each) 40198459000202 (case), Lot Numbers: 24EDA817; 6) REF CDS983498N, UDI/DI 10198459000188 (each) 40198459000189 (case), Lot Numbers: 24EDA816; 7) REF CDS983639J, UDI/DI 10195327228149 (each) 40195327228140 (case), Lot Numbers: 22IBF012, 22IBF004, 22LBE960, 22KBK687; 8) REF CDS983639K, UDI/DI 10195327351533 (each) 40195327351534 (case), Lot Numbers: 23EBA182, 23EBN996, 23CBV828, 23FBP157, 23FBH151; 9) REF CDS984267J, UDI/DI 10193489288872 (each) 40193489288873 (case), Lot Numbers: 22GBR052, 22FBG539, 22KBU660, 23ABL613, 23DBD827; 10) REF CDS984993N, UDI/DI 10195327031114 (each) 40195327031115 (case), Lot Numbers: 22EBV339; 11) REF CDS984993O, UDI/DI 10195327175764 (each) 40195327175765 (case), Lot Numbers: 22GBF349, 22JBJ441, 23BBV017, 23EBN595, 23IBU110, 23GBE740, 23GBE766, 23IBC614, 23LBC779, 23KBH710; 12) REF CDS984993P, UDI/DI 10195327588007 (each) 40195327588008 (case), Lot Numbers: 24ABH482, 24DBD860; 13) REF DYNJ00264L, UDI/DI 10193489942019 (each) 40193489942010 (case), Lot Numbers: 22IMH644, 22EMF495, 23AM
10195327497286, 40195327497287, 10198459000065, 40198459000066, 10195327497415, 40195327497416, 10195327497408, 40195327497409, 10198459000201, 40198459000202, 10198459000188, 40198459000189, 10195327228149, 40195327228140, 10195327351533, 40195327351534, 10193489288872, 40193489288873, 10195327031114, 40195327031115, 10195327175764, 40195327175765, 10195327588007, 40195327588008, 10193489942019, 40193489942010, 10195327333041, 40195327333042, 10193489954111, 40193489954112, 10195327291051, 40195327291052, 10193489442687, 40193489442688, 10195327089979, 40195327089970, 10195327089900, 40195327089901, 10195327187958, 40195327187959
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.