Recalls affecting Kentucky

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

D-0573-2022

Lot/product code:

lot# 25910009, Exp 01/2023

Recalling firm:

RISING PHARMACEUTICALS

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 #:

89684

Lot/product code:

Catalog Number: 12000650 UDI GTIN Code: 03610520653012 Lot Numbers: 301336

Recalling firm:

Bio-Rad Laboratories, 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 #:

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: 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: 00630414595580; Lot Numbers: 211359 211451

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 1.0 (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 #:

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 1.1 (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 #:

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 #:

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-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 #:

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-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 #:

F-0949-2022

Lot/product code:

Batches: 22331Z200 23377Z200 23438Z200 23439Z200 25562Z200 25562Z220 25563Z200 25729Z200 25730Z200 26731Z200 27922Z200 27931Z200 28124Z200 28125Z200 28126Z200 30291Z200 30292Z200 30517Z200 30518Z200 31392Z200 31402Z200 32421Z200 32684Z200 33694Z200 33695Z200 34012Z200 34769Z200 34770Z200 34771Z200 34771Z210 35023Z200 35032Z200 36149Z200 36150Z200 36151Z200 22331Z202 22331Z201

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-0950-2022

Lot/product code:

Batches: 24531Z200 26722Z200 26808Z200 26859Z200 28128Z200 28139Z200 28140Z200 30391Z200 34772Z200 34934Z200 36147Z200 24531Z201 28128Z201 30391Z201 34772Z201 36147Z201

Recalling firm:

Abbott Laboratories

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

Recall #:

F-0940-2022

Lot/product code:

Batches: 24447K807 24448K807 25674K800 25675K800 25677K800 25677K810 25798K800 26873K800 26874K800 26875K800 28024K800 28026K800 29247K800 29247K810 29248K800 29249K800 31502K800 31503K800 31504K800 33702K800 33703K800 33719K800 34854K800 34855K800 34856K800 34857K800 36100K800 36101K800 36102K800 36103K800

Recalling firm:

Abbott Laboratories

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

Recall #:

F-0956-2022

Lot/product code:

Batches: 26812Z261 29209Z201 30285Z263 32412Z222 33690Z201 26812Z262 27939Z263 29209Z203 30285Z262 32412Z223 26812Z263 27939Z260 29209Z200 30285Z260 32412Z220 32648Z200 26812Z260 27939Z261 29209Z202 30285Z261 32412Z221 33690Z200 33690Z210 27939Z262 29209Z204 30285Z264 32412Z224 33690Z202

Recalling firm:

Abbott Laboratories

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

Recall #:

F-0953-2022

Lot/product code:

Batches: 24532Z200 28129Z200 30400Z200 34935Z200 36154Z200

Recalling firm:

Abbott Laboratories

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

Recall #:

F-0943-2022

Lot/product code:

Batches: 33737SH00 33738SH00 33739SH00 35974SH00 35975SH00 36097SH00 36229SH01 32372SH00 32435SH00 32436SH00 36085SH00 36230SH00 37314SH00 32592K800 32595K800 35011K800 36138K800 36139K800 36231K800 36232K800 37291K800 37313K800

Recalling firm:

Abbott Laboratories

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

Recall #:

F-0920-2022

Lot/product code:

Batches: 31552Z200

Recalling firm:

Abbott Laboratories