Recalls affecting Indiana

FDA has not published a risk classification for this recall yet.

Recall #:

88991

Lot/product code:

GTIN: 08714729283805 Lot Numbers: 25612668, 25649812, 25704208, 25771760, 25878552, 26000695, 26010387, 26058284, 26087172, 26087173, 26123181, 26324742, 26366746, 26406513, 26429808, 26499853, 26527374, 26573853, 26638827, 26651718, 26665448, 26893604, 27026984, 27074109, 27145234, 27162321, 27255235, 27306699. Exp. 05/19/2022 to 05/13/2023

Recalling firm:

Boston Scientific Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88991

Lot/product code:

Batches: 25608761, 25640116, 25640117, 25644834, 25649819, 25649824, 25649829, 25649834, 25678825, 25678830, 25678835, 25678839, 25678880, 25680560, 25704230, 25704231, 25704232, 25739169, 25739170, 25806714, 25819946, 25819947, 25819948, 25836147, 25836148, 25850475, 25850476, 25850477, 25850478, 25850479, 25850540, 25850541, 25878986, 25878987, 25878988, 25878989, 25878990, 25878991, 25930854, 25940128, 25940129, 25940130, 25963979, 25969161, 25969162, 25975788, 25975789, 25975790, 25975791, 26010399, 26010400, 26047895, 26047896, 26047897, 26047898, 26047899, 26048760, 26058432, 26059172, 26123198, 26123199, 26123240, 26123241, 26123242, 26123243, 26123252, 26123253, 26175502, 26175503, 26175504, 26175505, 26207999, 26208000, 26208001, 26208002, 26208003, 26240379, 26247286, 26247287, 26247288, 26247289, 26284152, 26284153, 26284154, 26284155, 26284156, 26324769, 26324771, 26324773, 26324775, 26350409, 26356442, 26366767, 26366768, 26366769, 26366770, 26366771, 26366772, 26366773, 26366774, 26406539, 26406560, 26406561, 26406562, 26435589, 26435590, 26435591, 26440046, 26457040, 26457041, 26473800, 26473801, 26489988, 26491481, 26491482, 26491483, 26491484, 26499145, 26543699, 26545849, 26545850, 26545851, 26546369, 26549973, 26559545, 26581409, 26581410, 26581827, 26600543, 26600544, 26621751, 26628098, 26638074, 26651704, 26651705, 26651706, 26651709, 26674679, 26675080, 26675081, 26677000, 26677001, 26677002, 26686240, 26696688, 26696689, 26706795, 26706796, 26706797, 26718376, 26718377, 26739329, 26739331, 26739335, 26758738, 26759340, 26759342, 26760526, 26760527, 26760528, 26760529, 26779086, 26779087, 26779088, 26779089, 26779090, 26779092, 26779093, 26808304, 26808305, 26808306, 26808307, 26848733, 26848734, 26848735, 26848736, 26848737, 26888169, 26888170, 26888171, 26888172, 26919342, 26919343, 26919344, 26919345, 26940195, 26940196, 26940197, 26940198, 26990983, 26990984, 26990985, 26990986, 26990987, 26990988, 26990989, 26990990, 26990991, 27008809, 27008810, 27008811, 27008812, 27055019, 27055120, 27062059, 27065900, 27065901, 27074115, 27074116, 27121590, 27121591, 27121596, 27121598, 27121599, 27121626, 27148639, 27148780, 27148781, 27183303, 27183304, 27183305, 27183311, 27183312, 27219848, 27220333, 27233915, 27263158, 27263159, 27265233, 27265234, 27269980, 27269981, 27269982, 27308428, 27335462, 27347597, 27347598, 27384710, 27428069 GTIN: 08714729283874 Exp. 05/18/2022 to 06/03/2023

Recalling firm:

Boston Scientific Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88986

Lot/product code:

Catalys-U and Catalys-I with Windows 7 Ultimate/Professional/Embedded Standard. Catalys-C with Windows 7 Embedded Standard. 0160-6020 and 0160-6010 with Windows 7 Professional/Embedded Standard.

Recalling firm:

AMO Manufacturing USA, LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88986

Lot/product code:

G300 with Windows XP. G301 with Windows 7 Embedded System.

Recalling firm:

AMO Manufacturing USA, LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88923

Lot/product code:

Product Code/REF Number 2002-400; Lot codes: 441533, 443300, 443608, 443629, 444473, 445527, 448966, 449683, 450899, 450900, 451270, 451988, 452177, 452814, 454577, 455871, 458264, 458604, 459198, 459642, 462192, 462194, 464075, 464076, 465037, 466247, 469921, 470627, 471651,471703, 472562, 472785 and 473725.  UDI Code: 00650862100211

Recalling firm:

Atrium Medical Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88876

Lot/product code:

All serial numbers.

Recalling firm:

Thoratec Corp.

FDA has not published a risk classification for this recall yet.

Recall #:

88975

Lot/product code:

REF 72413575 - batch #21FM24289; REF 72413570 - batch #21GM04743.

Recalling firm:

Smith & Nephew, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

89050

Lot/product code:

Safe-T Lite

Recalling firm:

MAX LUX CORP

FDA has not published a risk classification for this recall yet.

Recall #:

88990

Lot/product code:

Product#/Brand Name/UDI Code: 450-0005-00 / OsteoMed OsteoPower Power Console 2i / 0084569401211 450-0021-00 / OsteoMed OsteoPower Power Console 2 / 0084569401215 450-0390 / OsteoMed BMF Footswitch / 0084569401215 450-0005-01 / OsteoMed D-Power Control Console 2i / 0084569401211 450-0021-01 / OsteoMed D-Power Control Console 2 / 0084569401211 ECOS-450-0021-00 / Power Control Console 2 / 0084569401211 ECOS-450-0005-00 / Power Control Console 2i / 0084569401211 Serial Numbers: 0332004 450-0005-01 0422006 450-0005-00 0423001 450-0005-01 0434003 S 0434004 S 0434010 S 0443004 0423005 450-0005-01 0449004s 0509004S 0509005S 0506027 0445003 0445005 9912003 0515009 0525014 0532001 0521042 0521045 0535006 0535007 0537031 0537032 0537033 0537034 0540005 0547022 0551022 0551025 0552008 0552009 0611004 0604070 0616001 0616002 0615005 0615009 0615010 0615039 0616003 0616005 0615041 0620004 0620005 0622022 0622023 0633024 0641004 0643068 0645002 0645003 0641009 0648023 0648025 0649002 0649003 0701004 0702021 0701005 0640004 0701006 0701009 0704036 0651097 0714001 0714002 0715029 0715031 0715032 0718003 0719005 0722041 0727024 0727025 0721005 0729044 0734030 0738015 0738017 0740001 0743032 0743033 0743034 0741013 0743036 0743037 0750022 0743038 0750023 0739022 0739023 0803016 0808001 0751032 0811002 0805025 0807056 0820004 0820004 0822030 0832057 0835005 0835004 0839048 0839048 0839049 0839049 0843053 0843054 0852046 0852002 0922072 0931001 0931003 0940011 0944016 0944006 0951020 0949001 1011002 1011003 1004051 1004052 1019002 1004054 1004055 1022048 1019005 1032001 1024002 1034007 1034008 1033010 1034009 1034010 1046013 1041033 1038009 1050036 1047020 1108032 1108033 1109006 1051004 1052014 1123010 1123012 1128022 1128023 1128026 1146012 1152006 0008006 9916005 1152007 1116005 1203041 1152008 1152009 1138003 1138005 1211003 9847002 1213003 1213004 1211005 1216001 1226008 1236044 1236040 1226007 1216002 1233042 1240054 1240055 1233041 1216005 1233045 1242003 1249002 1242004 1249003 1303005 1303002 1306002 1249005 1312002 1312003 1306004 1306005 1306001 0002001 1317012 0023005S 9916008 1240056 1317002 1317004 1336014 1340002 1340005 1341001 1341002 1346001 1346010 1346003 1349003 1349004 1341003 1349005 1351013 1346002 1405005 1405006 1420002 1420003 1405002 1417005 1424008 1424009 1424010 1417006 1434001 1434002 1434003 1434004 1441001 1441002 1441004 1445007 1445008 0244009 0720026 1509001 1509003 1516001 1516002 1518002 1521001 1521001 1521003 1521003 1528001 1528003 1528004 1528005 9942003 1533004 1533005 1528006 1537001 1537002 1537003 1539032 1539033 1539034 1547005 1547009 1543009 1553003 1543010 1604022 1604021 1614009 1134004 1614012 1614014 1604025 1604025 1610028 1610031 1610032 0603007 1410002 1620009 0232001 0548003 1622021 1604024 1610030 1622022 1622023 1622024 1638026 1634018 1634019 1638028 1638029 1634020 1634022 1638034 1638034 1634023 1634023 1634024 1634024 1634025 1634025 1639056 1639056 1639057 1639057 1639058 1644011 1644013 1643017 1644014 1644015 1644015 1643018 1651024 1651026 1644016 1651006 1707004 1707004 1707009 1707009 1651007 1651007 1710003 1710004 1651008 1651009 1651010 1651011 1712018 1710006 1710007 1711062 1711064 1711066 1711067 1715015 1651013 1711060 1711061 1715007 1715008 0751070 1719021 1719022 1719023 1711065 1713012 1721013 0651095 0051007S 1713013 1713014 1713015 1713016 1721015 1721016 1721017 1721018 1721019 1721014 1713017 1713018 1713019 1722009 1737018 1737017 1722011 1722012 1737019 1737020 1743001 1722013 1722014 1722015 1722016 1722017 1722018 1743009 1743007 1743008 1743010 1746027 1734014 1734015 1734016 1746031 1746030 1734017 1734018 1748010 1734019 1734020 1748009 1748001 1748003 1748006 1748007 1817052 1817053 1817054 1817055 1817056 1804002 1804010 1804001 1804003 1804004 1804005 1804007 1804006 1823017 1822008 1822010 1822014 1835012 1835013 1835020 1004053 1838001 1822015 1822016 1848001 1838003 1838004 1838005 1848002 1849017 1849019 1838006 1838007 1838008 1838009 1838010 1846025 1901001 1901002 1848003 1901003 1901004 1904003 1901009 1901010 1846026 1846027 1904001 1904002 1907011 1907012 1907013 1904004 1904005 1904006 1904007 1904008 1904009 1904010 1910031 1910032 1910033 1910034 1928046 1910035 1910036 1910037 1928047 1928048 1910039 1928049 1928050 1934001 1934002 1934003 1934004 1934005 1934006 1915001 1915002 1915003 1915004 1915005 1915006 1915007 1915008 1915009 1915010 1941001 1946002 1941002 1941003 1941004 1946003 1946004 1946005 2002034 1941005 2014016 2014017 2014018 2014019 2014020 1941006 2038001 2038002 1941007 1941008 2038003 2038004 2038005 2038006 2038007 2038008 1941009 2008002 2038009 2008003 2008004 2041001 0639018 2008005 2041002 2008001 2041003 2041006 2041007 2041008 2008007 2008008 2008009 2008010 2014001 2041009 2014002 2014003 2014004 ========================================================= -450-0380 / D-Bi-Directional Master Footswitch / 0084569401215 -450-0350 / D-Uni-Directional Footswitch II / 0084569401215 -450-0360 /… (truncated, 9865 characters total — see the official FDA record for the full value)

Recalling firm:

Osteomed, LLC

FDA has not published a risk classification for this recall yet.

Recall #:

95017

Lot/product code:

DI: 06430035872725, 06430035872732, 06430035872749, 06430035872756, 06430035872763, 06430035872770

Recalling firm:

Palodex Group Oy

FDA has not published a risk classification for this recall yet.

Recall #:

89044

Lot/product code:

Wireless foot switches Models: WFS Ad7(X) Option 3P 459801319471; WFS Ad7(X) Option 4P+2 459801319521; WFS Ad7(X) Option 3P 459801319361; WFS Ad7(X) Option 4P+2 459801319421; WFS Field Extension Set 3P (ORT) 459801319481; WFS Field Extension Set 4P+2 (ORT) 459801319531; WFS Field Extension Set 3P 459801319511; WFS Field Extension Set 4P+2 459801319541; WFS Field Extension Set Mono 459801319371; WFS Field Extension Set Biplane 459801319431; WFS Field Extension Set Mono (ORT) 459801319391; WFS Field Extension Set Biplane (ORT) 459801319441; Wireless Footswitch Set 3P 459801238241; Wireless Footswitch 3P 459801238231; Wireless Footswitch Set 4P+2 459801238261; Wireless Footswitch 4P+2 459801238251 Wireless Footswitch Set JP 459801238201; Wireless Footswitch 3P 459801238191; Wireless Footswitch Set 4P+2 459801238221; Wireless Footswitch 4P+2 459801238211; Wireless Footswitch 3P Kit 459801733051; Wireless Footswitch 3P Kit 459801733061; Wireless Footswitch 4P+2 Kit 459801733071; Wireless Footswitch 4P+2 Kit 459801733081; WFS Base Station 459801257861; WFS Base Station Kil 459801733091.

Recalling firm:

Philips North America Llc

FDA has not published a risk classification for this recall yet.

Recall #:

89001

Lot/product code:

All Lots manufactured between April 2015 to February 2021 UDI/Model No./Item No./Product Description: 812258020002 CPA1-000 PA0382-001 End Cap 887517001139 CPA2-000 PA1051-000 PACKAGED END CAP, 8.5/ 10.7MM, +0MM 887517001146 CPA2-005 PA1051-005 PACKAGED END CAP, 8.5/ 10.7MM, +5MM 887517001153 CPA2-010 PA1051-010 PACKAGED END CAP, 8.5/ 10.7MM, +10MM 887517001160 CPA2-015 PA1051-015 PACKAGED END CAP, 8.5/ 10.7MM, +15MM 887517001177 CPA2-020 PA1051-020 PACKAGED END CAP, 8.5/ 10.7MM, +20MM 887517001184 CPA3-000 PA1052-000 PACKAGED END CAP, 12.5MM , +0MM 887517001191 CPA3-005 PA1052-005 PACKAGED END CAP, 12.5MM , +5MM 887517001207 CPA3-010 PA1052-010 PACKAGED END CAP, 12.5MM , +10MM 887517001214 CPA3-015 PA1052-015 PACKAGED END CAP, 12.5MM , +15MM 887517001221 CPA3-020 PA1052-020 PACKAGED END CAP, 12.5MM , +20MM 812258028121 HEC1-000 PA0709-000 END CAP, 0MM HUMERAL NAIL 812258028138 HEC2-000 PA0709-002 END CAP, 2MM HUMERAL NAIL 812258028145 HEC3-000 PA0709-005 END CAP, 5MM HUMERAL NAIL 812258028152 HEC4-000 PA0709-010 END CAP, 10MM HUMERAL NAIL 812258028169 HEC5-000 PA0709-015 END CAP, 15MM HUMERAL NAIL 812258021337 LSB3-020 PP1699-020 Locking Screw, 3.5mm x 2 0mm 812258021344 LSB3-025 PP1699-025 Locking Screw, 3.5mm x 2 5mm 812258021351 LSB3-030 PP1699-030 Locking Screw, 3.5mm x 3 0mm 812258021368 LSB3-035 PP1699-035 Locking Screw, 3.5mm x 3 5mm 812258021375 LSB3-040 PP1699-040 Locking Screw, 3.5mm x 4 0mm 812258021382 LSB3-045 PP1699-045 Locking Screw, 3.5mm x 4 5mm 812258021399 LSB3-050 PP1699-050 Locking Screw, 3.5mm x 5 0mm 812258021405 LSB3-055 PP1699-055 Locking Screw, 3.5mm x 5 5mm 812258021412 LSB3-060 PP1699-060 Locking Screw, 3.5mm x 6 0mm 00887517029027 LSB3-200-S PA1220-020 3.5mm x 20mm Screw, Peg 00887517029010 LSB3-250-S PA1220-025 3.5mm x 25mm Screw, Peg 00887517029003 LSB3-300-S PA1220-030 3.5mm x 30mm Screw, Peg 00887517028990 LSB3-350-S PA1220-035 3.5mm x 35mm Screw, Peg 00887517028983 LSB3-400-S PA1220-040 3.5mm x 40mm Screw, Peg 00887517028976 LSB3-450-S PA1220-045 3.5mm x 45mm Screw, Peg 00887517028969 LSB3-500-S PA1220-050 3.5mm x 50mm Screw, Peg 00887517028952 LSB3-550-S PA1220-055 3.5mm x 55mm Screw, Peg 00887517028945 LSB3-600-S PA1220-060 3.5mm x 60mm Screw, Peg 856719002763 LSB4-020 PP1425-020 Locking Screw, 4.0mm x 20mm 856719002770 LSB4-025 PP1425-025 Locking Screw, 4.0mm x 25mm 856719002787 LSB4-030 PP1425-030 Locking Screw, 4.0mm x 30mm 856719002794 LSB4-035 PP1425-035 Locking Screw, 4.0mm x 35mm 856719002800 LSB4-040 PP1425-040 Locking Screw, 4.0mm x 40mm 856719002817 LSB4-045 PP1425-045 Locking Screw, 4.0mm x 45mm 856719002824 LSB4-050 PP1425-050 Locking Screw, 4.0mm x 50mm 856719002831 LSB4-055 PP1425-055 Locking Screw, 4.0mm x 55mm 856719002848 LSB4-060 PP1425-060 Locking Screw, 4.0mm x 60mm 856719002886 LSB5-020 PP1426-020 Locking Screw, 5.0mm x 20mm 856719002893 LSB5-025 PP1426-025 Locking Screw, 5.0mm x 25mm 856719002909 LSB5-030 PP1426-030 Locking Screw, 5.0mm x 30mm 856719002916 LSB5-035 PP1426-035 Locking Screw, 5.0mm x 35mm 856719002923 LSB5-040 PP1426-040 Locking Screw, 5.0mm x 40mm 856719002930 LSB5-045 PP1426-045 Locking Screw, 5.0mm x 45mm 856719002947 LSB5-050 PP1426-050 Locking Screw, 5.0mm x 50mm 856719002954 LSB5-055 PP1426-055 Locking Screw, 5.0mm x 55mm 856719002961 LSB5-060 PP1426-060 Locking Screw, 5.0mm x 60mm 856719002978 LSB5-065 PP1426-065 Locking Screw, 5.0mm x 65mm 856719002985 LSB5-070 PP1426-070 Locking Screw, 5.0mm x 70mm 856719002992 LSB5-075 PP1426-075 Locking Screw, 5.0mm x 75mm 812258021429 LSC4-020 PP1794-020 Locking Screw, 4.0mm x 2 0mm 812258021436 LSC4-025 PP1794-025 Locking Screw, 4.0mm x 2 5mm 812258021443 LSC4-030 PP1794-030 Locking Screw, 4.0mm x 3 0mm 812258021450 LSC4-035 PP1794-035 Locking Screw, 4.0mm x 3 5mm 812258021467 LSC4-040 PP1794-040 Locking Screw, 4.0mm x 4 0mm 812258021474 LSC4-045 PP1794-045 Locking Screw, 4.0mm x 4 5mm 812258021481 LSC4-050 PP1794-050 Locking Screw, 4.0mm x 5 0mm 812258021498 LSC4-055 PP1794-055 Locking Screw, 4.0mm x 5 5mm 812258021504 LSC4-060 PP1794-060 Locking Screw, 4.0mm x 6 0mm 00887517028938 LSC4-200-S PA1221-020 4.0mm x 20mm Screw, Peg 00887517028921 LSC4-250-S PA1221-025 4.0mm x 25mm Screw, Peg 00887517028914 LSC4-300-S PA1221-030 4.0mm x 30mm Screw, Peg 00887517028907 LSC4-350-S PA1221-035 4.0mm x 35mm Screw, Peg 00887517028891 LSC4-400-S PA1221-040 4.0mm x 40mm Screw, Peg 00887517028884 LSC4-450-S PA1221-045 4.0mm x 45mm Screw, Peg 00887517028877 LSC4-500-S PA1221-050 4.0mm x 50mm Screw, Peg 00887517028860 LSC4-550-S PA1221-055 4.0mm x 55mm Screw, Peg 00887517028853 LSC4-600-S PA1221-060 4.0mm x 60mm Screw, Peg 812258021511 LSC5-020 PP1742-020 Locking Screw, 5.0mm x 2 0mm 812258021528 LSC5-025 PP1742-025 Locking Screw, 5.0mm x 2 5mm 812258021535 LSC5-030 PP1742-030 Locking Screw, 5.0mm x 3 0mm 812258021542 LSC5-035 PP1742-035 Locking Screw, 5.0mm x 3 5mm 812258021559 LSC5-040 PP1742-040 Locking Screw, 5.0mm x 4 0mm 812258021566 LSC5-045 PP1742-045 Locking Screw, 5.0mm x 4 5… (truncated, 132877 characters total — see the official FDA record for the full value)

Recalling firm:

NuVasive Specialized Orthopedics, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

89509

Lot/product code:

Part Number 72754 UPC Code: 881608800397 EAN Code: 7331599999707 Lot Number: 33218501

Recalling firm:

Human Care USA, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

89509

Lot/product code:

Part Number 72755 UPC Code: 881608800403 EAN Code: 7331599999714 Lot Number: 33164504

Recalling firm:

Human Care USA, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MEQ001 21AEQ00 21BEQ001 21BEQ002 21BEQ003 21CEQ001 21DEQ001 21DEQ002 21EEQ001 21EEQ002 21FEQ001 21FEQ002 21GEQ001 21HEQ001 21HEQ002 21JEQ001 21JEQ002. UDI: 50192253018989 (cs) 10192253018981 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MBQ001 21ABQ001 21ABQ002 21BBQ002 21BBQ003 21BBQ004 21BBQ005 21CBQ002 21CBQ003 21DBQ003 21DBQ004 21DBQ005 21EBQ003 21EBQ004 21EBQ005 21FBQ002 21FBQ003 21FBQ004 21FBQ005 21HBQ001 21HBQ002 21JBQ002 UDI: 50192253018996 (cs) 10192253018998 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MFQ001 20MFQ002 20MFQ003 21AFQ001 21BFQ001 21BFQ002 21CFQ001 21CFQ002 21CFQ003 21DFQ001 21DFQ002 21EFQ001 21EFQ002 21FFQ001 21FFQ002 21GFQ001 21GFQ002 21GFQ003 21HFQ001 21JFQ001 UDI: 50192253018927 (Cs) 10192253018929 (Ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MLQ001 21BLQ001 21CLQ001 21DLQ001 21DLQ002 21ELQ001 21ELQ002 21ELQ003 21GLQ001 21HLQ001. UDI: 50192253006184 (cs) 10192253006186 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MDQ014 21ADQ007 21CDQ004 21CDQ005 21DDQ001 21DDQ002 21EDQ001 21FDQ001 21GDQ001 21HDQ001 21JDQ003. UDI: 50192253018972 (cs) 10192253018974 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 21CKQ001 21CKQ002 21HKQ001. UDI: 50192253005941 (cs) 10192253005943 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MFQ001 20MFQ002 20MFQ003 21AFQ001 21BFQ001 21BFQ002 21CFQ001 21CFQ002 21CFQ003 21DFQ001 21DFQ002 21EFQ001 21EFQ002 21FFQ001 21FFQ002 21GFQ001 21GFQ002 21GFQ003 21HFQ001 21JFQ001 UDI: 50885380172500 (cs) 10885380172502 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MJQ001 20MJQ002 21AJQ001 21AJQ002 21AJQ003 21AJQ004 21AJQ005 21AJQ006 21BJQ001 21BJQ002 21CJQ001 21DJQ001 21DJQ002 21DJQ003 21EJQ001 21EJQ002 21EJQ003 21EJQ004 21FJQ001 21FJQ002 21FJQ003 21GJQ001 21GJQ002 21HJQ001 21HJQ002 21HJQ003 21HJQ004 21HJQ005 21HJQ006 21JJQ001 21JJQ002 21JJQ003 UDI: 50885380172494 (cs) 10885380172496 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MMQ007 21BMQ007 21CMQ008 21DMQ001 21EMQ003 21FMQ007. UDI: 50192253006191 (cs) 10192253006193 (ea)

Recalling firm:

Cardinal Health

FDA has not published a risk classification for this recall yet.

Recall #:

88981

Lot/product code:

All serial numbers. UDI: 04953170339967

Recalling firm:

Olympus Corporation of the Americas

FDA has not published a risk classification for this recall yet.

Recall #:

89015

Lot/product code:

Lot Numbers: 20MMQ004 20MMQ005 20MMQ006 21AMQ005 21AMQ006 21BMQ006 21CMQ004 21CMQ005 21CMQ006 21CMQ007 21FMQ003 21FMQ004 21HMQ002 21HMQ006. UDI: 50192253006177 (cs) 10192253006179 (ea)

Recalling firm:

Cardinal Health