Recalls affecting Kansas

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

Recall #:

89684

Lot/product code:

Catalog Number: 12000651 UDI GTIN Code: 03610520652770 Lot Numbers: 53262

Recalling firm:

Bio-Rad Laboratories, Inc.

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

Recall #:

89740

Lot/product code:

UDI: 00630414595580; Lot Numbers: 211359 211451

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

89740

Lot/product code:

UDI: 00630414220697; Lot Numbers: 211392 211438 211484 211522 211526

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

89740

Lot/product code:

UDI: 00630414287935; Lot Numbers: 110108 110185 110238 110302

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

89740

Lot/product code:

UDI: 00630414220505; Lot Numbers: 110027 110060 110065 110091 110113 110129 110137 110161 110170 110208 110224 110234 110235 110262 110265 110273 110286 110315 110330 110347 110360

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

89744

Lot/product code:

UDI# 00607567700901, Lots (3): 25153700, 25157489, 25158616. Please note affected lot numbers (25153700, 25157489, 25158616) appear on the device package only. If the packaging has been discarded, the affected devices can be identified by Device Component Lot number (200501), which is etched onto all 3 device components on side of handle and on underside above each pin.

Recalling firm:

Maquet Cardiovascular, LLC

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

Recall #:

93819

Lot/product code:

Model: R90 1.1 (709031); UDI DI: 00884838101456; Software version 1.1.1 or higher; Serial Numbers: 10001004, 10001005, 10001006, 10001008, 10001009, 10001010, 10001011, 10001012, 10001013, 10001018, 10001020, 10001022, 10001024, 10001026, 10001027, 10001028, 10001029, 10001030, 10001031, 10001032, 10001035, 10001036, 10001043, 10001044, 10001045, 10001046, 10001047, 10001048, 10001049, 10001050, 10001051, 10001052, 10001053, 10001054, 10001055, 10001056, 10001057, 10001058, 10001059, 10001060, 10001061, 10001062, 10001063, 10001064, 10001065, 10001066, 10001067, 10001068, 10001069, 10001070, 10001071, 10001072, 10001073, 10001074, 10001075, 10001076, 10001077, 10001078, 10001079, 10001080, 10001081, 10001083, 10001084, 10001085, 10001086, 10001087, 10001088, 10001089, 10001090, 10001091, 10001092, 10001093, 10001094, 10001095, 10001096, 10001097, 10001098, 10001099, 10001100, 10001101, 10001102, 10001103, 10001104, 10001105, 10001106, 10001107, 10001108, 10001109, 10001110, 10001111, 10001112, 10001113, 10001114, 10001115, 10001116, 10001117, 10001118, 10001119, 10001120, 10001121, 10001122, 10001123, 10001124, 10001125, 10001126, 10001127, 10001128, 10001129, 10001130, 10001131, 10001132, 10001133, 10001134, 10001135, 10001136, 10001137, 10001138, 10001139, 10001140, 10001141, 10001142, 10001143, 10001144, 10001145, 10001147, 10001148, 10001149, 10001150, 10001152, 10001201;

Recalling firm:

PHILIPS MEDICAL SYSTEMS

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

Recall #:

89822

Lot/product code:

UDI # 07350002010020, 07350002010013, 07350002010082, 07350002010075, 07350002010242, 07350002010068, 07350002010112, 07350002010136, 07350002010129, 07350002010204, 07350002010235, 07350002010174, 07350002010266, 07350002010297, 07350002010303, 07350002010365, 07350002010310, 07350002010471, 07350002010389, 07350002010433, 07350002010440, 07350002010426

Recalling firm:

RaySearch America Inc

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

Recall #:

93819

Lot/product code:

Model: R90 1.0 (709030); UDI DI: 00884838076747; Software version 1.1.1 or higher; Serial numbers: 10000000, 10000002, 10000003, 10000004, 10000006, 10000011, 10000012, 10000020, 10000024, 10000027, 10000049, 10000050, 10000065, 10000066, 10000067, 10000069, 10000078, 10000081, 10000099, 10000103, 10000107, 10000140, 10000145, 10000152, 10000180, 10001001, 10001010, 10001095, 591362, SN16000009, SN17000003, SN17000007, SN17000015, SN17000022, SN17000111, SN17000114, SN17000118, SN17000120, SN17000121, SN17000122, SN17000123, SN17000128, SN17000129, SN17000130, SN17000145, SN17000146, SN17000147, SN17000148, SN17000153, SN17000157, SN17000163, SN17000165, SN17000166, SN18000003, SN18000004, SN18000010, SN18000021, SN18000025, SN18000033, SN18000037, SN18000038, SN18000044, SN18000045, SN18000053, SN18000054, SN18000057, SN18000060, SN18000068, SN18000069, SN18000079, SN19000004, SN19000006, SN19000011, SN19000020, SN19000034, SN19000036, 27, 40, 41, 42, 77, 101, 131, 155, 180, 190;

Recalling firm:

PHILIPS MEDICAL SYSTEMS

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

Recall #:

89666

Lot/product code:

UDI: 00840733102318 All units in the field, all serial numbers.

Recalling firm:

Meridian Bioscience Inc

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

Recall #:

90129

Lot/product code:

Lot Number 101321021B

Recalling firm:

Luminex Corporation

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

Recall #:

89731

Lot/product code:

PAT.003 (KR), PAT.006 (US), PAT.107 (EU), PAT.108 (US), PAT109 (US), PAT.110 (US), PAT.111 (EU), PAT.112 (US), PAT.113 (US), PAT.114 (EU), PAT.115 (EU), SAT.116 (US), SAT.117 (EU), SAT.118 (RU), SAT.119 (US), SAT.120 (EU), SAT.122 (EU), SAT.123 (US), SAT.125 (IN), SAT.126 (US), SAT.127 (TW), SAT.132 (EU), SAT.133 (US), SAT.136 (IN), SAT.140 (US), SBF.101 (EU), SBF.103 (JP), SBF.104 (JP), SBF.105 (US), SBF.107 (FR), SBF.109 (UK), SBF.110 (UK), SBF.112 (EU), SBF.113 (US), SBF.115 (UK), SBF.117 (EU), SBF.128 (US).  UDI: (01)05404013801138

Recalling firm:

Ion Beam Applications S.A.

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

Recall #:

89655

Lot/product code:

Lot #583-21 and higher, UDI 10837461002611.

Recalling firm:

Beckman Coulter, Inc.

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

D-0207-2024

Lot/product code:

All lots, expiry on or before August 2023

Recalling firm:

TCP HRB ACQUISITON LLC

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

D-0208-2024

Lot/product code:

All lots, expiry on or before August 2023

Recalling firm:

TCP HRB ACQUISITON LLC

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

D-0209-2024

Lot/product code:

All lots, expiry on or before August 2023

Recalling firm:

TCP HRB ACQUISITON LLC

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0933-2022

Lot/product code:

Batches: 32624SH00 34958SH00 25673SH00 31463SH00 31549SH00 32625SH00 32626SH00 25604K800 31454K800 35008K800 37251K800 35055SH00 35056SH00 32624SH01 32625SH01 32626SH01

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0935-2022

Lot/product code:

Batches: 23432SH00 23433SH00 24461SH00 24462SH00 25593SH00 25594SH00 25596SH00 26765SH00 26766SH00 26795SH00 26796SH00 27001SH00 27003SH00 27996SH00 27997SH00 27998SH00 28025SH00 28111SH00 29229SH00 29230SH00 30359SH00 31585SH00 31587SH00 31588SH00 35059SH00 35072SH00 37245SH00 23403K800 23404K800 23406K800 23408K800 23410K800 23434K800 23435K800 23436K800 23437K800 24473K800 24474K800 24475K800 24476K800 24477K800 24478K800 24491K800 24492K800 24512K800 24513K800 24514K800 24518K800 24519K800 24520K800 24521K800 24522K800 25578K800 25580K800 25581K800 25582K800 25583K800 25584K800 25585K800 25597K800 25599K800 25601K800 25602K800 25603K800 25666K800 25669K800 25670K800 25671K800 25672K800 25680K800 25696K800 25697K800 25698K800 25699K800 26751K800 26753K800 26754K800 26755K800 26757K800 26757K801 26758K800 26775K800 26776K800 26792K800 26793K800 26794K800 26844K800 26845K800 26846K800 26847K800 26848K800 26849K800 26850K800 26851K800 27002K800 27894K800 27895K800 27896K800 27897K800 27898K800 27899K800 27900K800 27901K800 27902K800 27903K800 27904K800 27905K800 27906K800 27907K800 27908K800 27909K800 27962K800 27963K800 27964K800 27965K800 27966K800 27967K800 27968K800 27969K800 27969K810 27970K800 27999K800 28004K800 28005K800 28006K800 28007K800 28009K800 28011K800 28028K800 28030K800 28084K800 28085K800 28093K800 28094K800 28095K800 28107K800 28108K800 28109K800 28110K800 28112K800 28113K800 28114K800 28115K800 28116K800 28149K800 28150K800 28151K800 29196K800 29197K800 29198K800 29199K800 29200K800 29207K800 29208K800 29221K800 29223K800 29224K800 29227K800 29250K800 29251K800 29252K800 29253K800 29254K800 29255K800 29256K800 29257K800 30310K800 30324K800 30346K800 30347K800 30348K800 30350K800 30352K800 30354K800 30366K800 30367K800 30368K800 30370K800 30371K800 30373K800 31477K800 31479K800 31485K800 31487K800 31489K800 31491K800 31505K800 31506K800 32596K800 32621K800 32622K800 32623K800 32634K800 32635K800 32637K800 32678K800 32679K800 33786K800 33787K800 33788K800 33789K800 33790K800 33791K800 33832K800 33833K800 34793K800 34795K800 34797K800 34811K800 34813K800 34814K800 34816K800 34817K800 34818K800 34819K800 34820K800 34852K810 34853K810 34863K800 34864K800 34875K800 34876K800 34877K800 34878K800 34879K800 34880K800 34881K800 34882K800 34883K800 34936K800 34937K800 34938K800 34939K800 34941K800 34942K800 34951K800 34952K800 34953K800 34954K800 35070K800 35071K800 35984K800 35985K800 35986K800 36087K800 36140K800 36141K800 36142K800 36143K800 36225K800 36226K800 36227K800 36228K800 37242K800 37243K800 32640SH00 23405SH00 23405SH01 24527SH00 24569SH00 25693SH00 26836SH00 27880SH00 28147SH00 28148SH00 29183SH00 29184SH00 32593SH00 37246SH00 37247SH00 37248SH00 37249SH00 37250SH00 37309SH00 37310SH00

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0932-2022

Lot/product code:

Batches: 30343SH00 34959SH00 24494SH00 30343SH01 32594SH00 32594SH10 32594SH20 34799SH00 34959SH01

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0947-2022

Lot/product code:

Batches: 30349SH00 30351SH00 30353SH00 32461SH00 36095SH00 34955SH00 34956SH00 34956SH01 34957SH00 36217SH00 32355K800 32464K800 35076K800 35077K800 36136K800 36137K800

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0945-2022

Lot/product code:

Batches: 24397K800 27994SH00 27995SH00 24400SH00

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0924-2022

Lot/product code:

Batches: 28091SH00 35007SH00 24493SH00 26773SH00 27992SH00 28174SH00 31495SH00 34815SH00 36099SH00 37294SH00

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0955-2022

Lot/product code:

Batches: 25558Z260 27940Z260 29267Z260 33689Z200 35026Z260

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0936-2022

Lot/product code:

Batches: 33688Z201 34929Z202 35065Z201 36145Z202 29280Z260 32430Z200 36145Z201 28123Z262 33688Z202 23443Z261 25659Z260 30283Z260 31410Z200 31411Z201 32431Z200 25659Z261 28123Z261 30283Z262 31410Z204 25659Z262 26867Z262 28123Z263 29210Z202 30283Z263 33688Z203 35065Z202 29210Z201 33688Z204 23443Z260 25550Z260 25564Z260 26867Z260 27936Z260 27937Z260 28123Z260 29210Z200 29280Z261 30281Z260 30283Z261 31410Z201 31410Z205 31410Z206 31411Z200 32423Z200 32431Z201 33688Z200 34929Z200 35030Z200 35049Z200 35065Z200 35066Z260 36145Z200 25550Z261 26867Z261 32423Z201 32431Z202 34929Z201

Recalling firm:

Abbott Laboratories

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

F-0944-2022

Lot/product code:

Batches: 24399SH00 33780SH00

Recalling firm:

Abbott Laboratories