Alcon or Endure Ophthalmic Microscope Product Usage recall

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model: LuxOr E71 and E71 Q-Vue 8065752304, 8065752323, 8065752332, and 8065752333 US Serial numbers: 22013, 1401148103X, 1401148201X, 1401148204X, 1401554606X, 1401845004X, 1401845005X, 1401974102X, 1401974104X, 1401974105X, 1401977002X, 1401977003X, 1402067603X, 1402067604X, 1402067605X, 1402149501X, 1402149503X, 1402149504X, 1402167704X, 1402249701X, 1402249702X, 1402249703X, 1402249803X, 1402314601X, 1402314701X, 1402314705X, 1402355101X, 1402677604X, 1402804905X, 1402877605X, 1402877701X, 1402877702X, 1402877801X, 1402877804X, 1402959102X, 1402959201X, 1402959202X, 1402959204X, 1403031005X, 1403133802X, 1403133804X, 1403133805X, 1403353401X, 1403353402X, 1403353403X, 1403353404X, 1403353405X, 1403571101X, 1403571102X, 1403571103X, 1403571104X, 1403571105X, 1403701202X, 1403701203X, 1403701204X, 1403701205X, 1403701206X, 19941, 20214, 20349, 20381, 20585, 20652, 20702, 20714, 20722, 20781, 20832, 20862, 20878, 20878-2, 20879, 20933, 21017, 21019, 21032, 21104, 21171, 21173, 21217, 21270, 21463, 21516, 21567, 21590, 21630, 21639, 21654, 21678, 21749, 21750, 21815, 21849, 21867, 21940, 21972, 22003, 22026, 22029, 22088, 22088-2, 22134, 22182, 22231, 2713, 30131, 30216, 30363, 30363-2, 30766, 31172, 31172-2, 3157, 31646, 31745, 31780, 31873, 31873-2, 31873-3, 32004, 32214, 32347, 32384, 32384-2, 32400, , 32420, 32420-2, 32439, 32453, 32553, 32568, 32643, 32694, 32694-2, 32698, 32743, 32748, 32755, 32771, 32785, 32785-2, 32785-3, 32875, 32886, 32886-2, 32896, 32909, 32923, 32923-2, 32994, 33028, 33039, 33176, 33176-2, 33263, 33270, 33313, 33325, 33348, 33348-2, 33355, 33358, 33392, 33392-2, 33440, 33442, 33454, 33460, 33464, 33498, 33498-2, 33522, 33535, 33592, 33598, 33606, 33606-2, 33606-3, 33606-4, 33653, 33769, 33775, 33783, 33849, 33850, 33850-2, 33892, 33904, 33926, 33966, 33999, 34030, 34030-2, 34033, 34099, 34099-2, 34173, 34203, 34204, 34280, 3431 1, 34312, 34352, 34352-2, 34371, 34458, 34458-2, 34468, 34556, 34562, 34564, 34597, 34616, 34627, 34627-2, 34627-3, 34679, 34680, 34682, 34682-2, 34686A-2, 34699, 34700, 34701, 34780, 34884, 34911, 34951, 34956, 34974, 34999, 34999-2, 35010, 35039, 35061, 35063, 35063-2, 35064, 35120, 35144, 35149, 35162, 35163, 35203, 35266, 35288, 35289, 35316, 35330, 35334, 5382, 35382-2, 35383, 35433, 35433-2, 35433-3, 35433-4, 35450, 35462, 35511, 35553, 35572, 35602, 35615, 35616, 35616-2, 35644, 35690, 35690-2, 35696, 35742, 35742-2, 35785, 35786, 35789, 35789-2, 35791, 35827, 35833, 35855, 35860, 35860-2, 35886, 35893-4, 35919, 35967, 35969, 35969-2, 35981, 35985, 35985-2, 35993, 36013, 36013-2, 36014, 36021, 36022, 36031, 36031-2, 36077, 36078, 40220 :002, 40220:004, 40220:006, 40232:00, 40476, 40514:001, 40516 :001, 40518:001, 40545 :003, 40547:003, 40548:003, 40609:003, 40612:003, 40680:001, 40681 :001, 40684:001, 40685 :001, 40687:001, 40688:001, 40769:001, 40770:001, 40773 :001, 40776:001, 40778 :001, 40781:001, 40783:001, 40797 :001, 40798 :001, 40801 :001, 40803:001, 40804:001, 40806 :001, 40807:001, 40837:003, 41147 :001, 41151 :001, 41153:001, 41190:001, 41212:001, 41256 :001, 4157 :001, 41266:001, 41270 :001, 41272 :001, 41273:001, 41481 :001, 41612:001, 41613 :001, 41842:001, 41853 :001, 41858:001, 41859 :001, 41860 :001, 41865 :001, 42109 :001, 42111 :001, 42321:001, 42334:001, 42345 :001, 42346 :001, 42497 :001, 42498 :001, 42500:001, 42507 :001, 42883 :001, 43178 :001, 43179 :001, 43241 :001, 43638 :001, 3640 :001, 43680 :001, 43685 :001, 43690 :001, 43691 :001, 3692 :001, 43693 :001, 43813 :001, 43814:001, 43816 :001, 43821 :001, 44025 :001, 44063 :001, 44083 :001, 44084 :001, 4090 :001, 44097 :001, 44299 :001, 44306 :001, 44308 :001, 44310 :001, 44313 :001, 44314 :001, 44357 :001, 44358 :001, A005, A006, A012, A014, A016 and A018 OUS Serial Numbers: 41242:001, 41275 :001, 41848 :001, 1401148001X, 1401148101X, 1401148104X, 1402643103X, 1402314404X, 1402314405X, 1403918102X, 1502158505X, 42119:001, 42994 :001, 44040:001, 43232 :001, 1401975304X, 1402388004X, 43238:001, 43240:001, 41841 :001, 41258 :001, 1401554610X, 1401954603X, 1402067602X, 1402677602X, 41891:001, 43000 :001, 43246:001, 43487 :001, 43546 :001, 43547 :001, 43566 :001, 1401148203X, 1402250002X, 1403600301X, 1403600305X, 1501088505X, 1501247401X, 1501247403X, 1401148105X, 43947 :001, 44027 :001, 41225 :001, 42348 :001, 42998 :001, 43002 :001, 43167 :001, 1401148202X, 41140 :001, 42201:001, 43045 :001, 43400 :001, 42793 :001, 42796 :001, 1501355802X, 43548 :001, 1401554603X, 1401579101X, 1401579103X, 1401831601X, 1401991002X, 1403211805X, 1502004802X, 43557:001, 43633:001, 43645:001, 44058:001, 44060:001, 44093:001, 44095:001, 44096:001, 1402643102X, 42115:001, 1401975302X, 1402677603X, 1402677605X, 1403133905X, 1501088502X, 1501088506X, 1501088507X, 1501088508X, 1501247402X, 40610 :003, 41070:001, 41073:001, 41143:001, 41226:001, 41240 :001, 41627 :001, 41628:001, 43234:001, 43236 :001, 43237 :001, 43239:001, 44054:001, 1402388002X, 101200157, 1403331702X, 1403331805X, 43256 :001, 43549 :001, 41619 :001, 42797 :001, 43172 :001, 43301 :001, 41631:001, 41632 :001, 1402677601X, 41616 :001, 1402249804X, 1402314402X, 40611 :003, 40853:002, 41261:001, 41854:001, 42114:001, 42347 :001, 42588:001, 42608 :001, 43486 :001, 43644 :001, 1401554608X, 41688:001, 43173 :001, 43177-001, 43229:001, 43683:001, 42105 :001, 42107:001, 42108 :001, 43789:001, 43790 :001, 43791 :001, 44048 :001, 44049 :001, 44050 :001, 42503 :001, 1401554509X, 40805 :001, 41482 :001, 41611 :001, 41846 :001, and 42110 :001.

Product

Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic surgical procedures for cataract…

Recalling firm

Alcon Research Laboratories Ltd.

Quantity

544 (399 units to USA)

Distribution

Worldwide Distribution - US Nationwide Distribution in the states of AK, AL, AR, AZ, CA, CO, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, Ml, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, Puerto Rico and US Virgins Islands Australia, Austria, Bahamas, Belarus, Canada, Chile, Colombia, Czech Republic, Denmark, Dominican Republic, Ecuador, El Salvador, Finland, Germany, Guatemala, India, Indonesia, Italy, Jamaica, Japan, Kenya, Lebanon, Mexico, Netherland Antilles, Norway, Peru, Philippines, Poland, Romania, Slovakia, Spain, Sri Lanka, Sweden, Taiwan, Thailand, Ukraine, United Kingdom, and Vietnam

Recall date

March 6, 2019

Classification

Class II

Status

Terminated

Agency

FDA (device)