Recalls affecting Illinois

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

Recall #:

H-1195-2026

Lot/product code:

Item No. CKJ19067 Lot: 20251106Z1-1 Expiration: NOV/05/2026

Recalling firm:

Big Way Ca Inc

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

Recall #:

D-0733-2026

Lot/product code:

Batch # DMC125018A, Exp Date: 07/2027.

Recalling firm:

Aurobindo Pharma USA Inc

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

Recall #:

D-0731-2026

Lot/product code:

Lot #: 19260937A, Exp. Date February 2028; 19261225A, 19261185A, Exp. Date March 2028; 19261664A, 19261682A, Exp. Date April 2028.

Recalling firm:

Glenmark Pharmaceuticals Inc., USA

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

Recall #:

99467

Lot/product code:

UDI: 10705034645995/Serial Numbers: W14316295301 W15316297501 W15316298001 W17316322901 W17316323301 W21316347401 W21316347501 W21316347601 W21316347801 W21316347901 W21316348001 W22316365801 W34316479001 W34316479101 W34316479201 W34316479301 W34316479401 W34316479601 W34316479801 W34316480001 W34316480101 W49316554301 W51316597001 W51316597101 Y03316603601 Y03316603701 Y03316603801 Y07316625901 Y15316690901

Recalling firm:

Medos International Sarl

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

Recall #:

D-0730-2026

Lot/product code:

Lot # DLHU0031, Exp Date: 06/30/2027.

Recalling firm:

MICRO LABS USA INC

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

Recall #:

99529

Lot/product code:

UDI (01)00854904006008(10)0704310, Serial Numbers: CV-00272120, CV-0080080176, CV-01318490, CV-01-80102732, CV-80057523, CV-00494020-38

Recalling firm:

FUJIFILM Healthcare Americas Corporation

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

Recall #:

99520

Lot/product code:

Software version V9.5 - UDI (01)00842000101239(10)9.5.0(11)260409

Recalling firm:

Merge Healthcare, Inc.

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

Recall #:

99561

Lot/product code:

UDI-DI 10193489431070 Lots 25BBB005 25GBY063 25KBI862 25LBT688 26CBG211

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

UDI-DI 10889942925858 Lot 26EBI940

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

CDS981762B UDI-DI 10193489306767 Lots 24JBE456 24JBN932 24KBJ154 25ABK513 25CBL684 25HBK086 25IBM188 25KBL720 25LBF812 25LBU497 26ABM665 26CBH544 26CBT272 26FBK806 DYKA1054F UDI-DI 10193489312607 Lots 24ILA823 24JLA285 24LLA226 24LLB033 25BLA842 25ELA624 25GLA270 25HLB055 25KLA019 25KLA187 26BLA150 26CLA717 26DLA410 26ELA772 26FLA756

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

DYKS1583A UDI-DI 10198459146640 Lot 24KBP388

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

DYKS2018 UDI-DI 10198459188480 Lot 25GMI043 DYKS1584A UDI-DI 10198459146633 Lots 24JBA740 25ABF244 DYKS1216I UDI-DI 10198459362668 Lots 25GBP888 25JBD789 26ABL474 26CBF334 26DBD640 26EBB855 26FBC632 DYKM1398B UDI-DI 10198459413827 Lots 25HBI183 25JBK222 25KBA990 25LBJ990 26BBI525 26CBJ249 26EBQ630 26FMF189

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

DYNDH1487A UDI-DI 10193489484311 Lots 25AMD225 25BMA495 25GMD834 25HMJ685 26AMD781 26DMI370 26FMG952 26FMJ739

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

CDS983348AA UDI-DI 10195327385088 Lots 24IBK346 24JBK539; CDS983348AB UDI-DI 10198459136986 Lots 25CBF097 25HBB232 25HBB761 25HBH209 25HBU907 25JBQ176

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

CDS860014Q UDI-DI 10198459629822 Lots 26ABR359 26BBP789 26CBL940 26DBK987 26FBK255 26FBK816 DYKM1000B UDI-DI 10889942508143 Lots 24KMD782 24LMH404 25AMD765 25BMD744 CDS860014P UDI-DI 10888277797819 Lots 24IBA155 24JBY045 24LBM014 25HBR509 25JBX951 DYNDV2684 UDI-DI 10198459185465 Lot 24LBP243

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

DYKA1384B UDI-DI 10198459415753 Lot 25GBS617 DYKA1384C UDI-DI 10198459485206 Lot 25IBF898 DYKS1206D UDI-DI 10198459414794 Lots 25HBI181 25JBJ452 25LBJ223 26ABT372 26CBF527 26EBH733

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

DYNDV1875 UDI-DI 10888277860209 Lot 24JMB689 ACC010972 UDI-DI 10198459303289 Lots 25DDA151 25DDA401 25EDA655 ACC010479A UDI-DI 10195327131517 Lot 25BDB620 ACC010690 UDI-DI 10195327433307 Lots 24LDB023 25BDA230 25GDA245 25JDB903 25KDB182 25LDA088 25LDA809 26ADC073 26CDA991 26DDB182 26EDA950 26EDB485 26FDB456 ACC010875 UDI-DI 10198459113659 Lots 24JDA648 25CDB776 25JDB205 25KDB028 25LDB271 26DDA182 26DDA786 26EDA629 ACC011073 UDI-DI 10198459569333 Lot 25LDA072 ACC011088 UDI-DI 10198459589577 Lots 26BDA548 26GDA090 ACC011067 UDI-DI 10198459529184 Lots 25KDA639 25LDA980 26CDB158 DYKM1564 UDI-DI 10889942754571 Lots 24HBW937 24JBX634 24LBR085 25GBH209 25IBK590 25LBD525 26ABI524 26BBM585 26DBC555 DYKM1564A UDI-DI 10198459805165 Lot 26FBK649 DYNJT10325 UDI-DI 10198459787324 Lots 26EBM250 26FBA470 26FBF055 26FBH553 26FBH554 DYKS1089B UDI-DI 10193489306286 Lots 24JMG846 24LMD918 25GMD759 25GMK431 25IMF050 25KMJ026 26BMC073 26DMI048 DYNJ63410 UDI-DI 10193489737431 Lots 24LDB851 25BDA890 DYNDH1363 UDI-DI 10888277795464 Lots 24IBH349 24IBS200 24JBQ160 24KBN447 24LBG380 24LBI547 25ABW563 25DBH954 25GBD824 25HBT172 25IBO192 25JBB921 25JBQ987 ACC010770 UDI-DI 10195327576998 Lots 25HDA878 25IDA087 25IDA817 25JDB317 25KDB340 25LDB061 26ADA012 26ADA159 26ADB380 26ADC072 26BDA633 26CDA678 DYNDH1591 UDI-DI 10193489497236 Lots 24JMA966 25GMD752 25LMJ154 26AME497 26BMA252 26DMI088 26EMH914 26FMH453 26FMK588 EDUC1043 UDI-DI 10195327425531 Lots 24KDA258 24KDA880 24KDA963 EDUC1043A UDI-DI 10198459334559 Lots 25FLA817 25GLA090 25KLA077 25KLA693 26CLB165 26CLB165Z 26ELA472 DYKM1496 UDI-DI 10889942636082 Lot 24KBL243 DYNDV2520 UDI-DI 10653160384045 Lot 2024111990

Recalling firm:

Medline Industries, LP

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

Recall #:

99561

Lot/product code:

DYNDH1444D UDI-DI 10195327502492 Lots 24IBK133 24KBE072 24LBD419 25GBT189 25IME347 25IMI389 25KMA880 25KME693 26BMH685 26CMH411 26DME199 26EMB070 26EMF542 26FMC275 DYNDH1866 UDI-DI 10195327400958 Lots 24HBW237 24IBI505 24JBI308 24KBH534 24LBI545 25ABC487 25ABO282 DYNDH1462B UDI-DI 10195327662462 Lots 24HBV192 24IBE469 24IBV947 24JBA557 24JBI310 24KBJ830 24KBJ831 24KBN934 24LBN283 24LBP258 DYNDH1622C UDI-DI 10195327509873 Lots 24IBE381 24IBL908 24JBF575 24JBS022 24KBN937 24LBI552 DYNDH1622D UDI-DI 10198459234965 Lots 25GBA905 25GBI398 25GBT182 25HBN203 25IBH345 25IBQ486 25IBS192 25JBN629 25KBK718 25LBI568 DYNDH1622F UDI-DI 10198459658884 Lots 26BBL477 26CBA407 26CBD376 26DBA855 26DBL286 26FBF458 DYNDH1715B UDI-DI 10195327407094 Lot 24IMF148 DYNDH2028 UDI-DI 10198459035715 Lot 24KBL250 DYNDH2048 UDI-DI 10198459106125 Lots 24JBK987 25GBI401 25GBT183 25IBB666 25JBC742 25KBD093 25KBK723 25LBI567 25LBO863 26ABL653 26CBO165 26DBB153 26DBE994 26EBF752 26FBN334 DYNDH2089 UDI-DI 10198459244070 Lots 25KMJ967 26BMI731 26FMF126 DYLAB1081 UDI-DI 10198459199608 Lots 24LMH506 25HMA386 25HMD685 25IMF415 25JMB438 25JMC503 26AML138 26BMJ277 26EMB352 DYLAB1080 UDI-DI 10198459199615 Lots 24LMG085 25AMH560 DYNDH1445C UDI-DI 10195327502614 Lots 24IBK131 24KBB551 24LBU139 25GBQ023 25GBU016 25HMI515 25IMB465 25IME350 25JMI247 26CMB609 26DMH686 26FMC274 26FMC274D DYNDH2350 UDI-DI 10198459779251 Lot 26FBM766 DYNDH2093 UDI-DI 10198459256967 Lot 26ABP408

Recalling firm:

Medline Industries, LP

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

Recall #:

99404

Lot/product code:

Lot Code: This correction affects IQecg plugin software versions starting with v10 and prior to v10.1.0.18 installed on Midmark IQecg Digital ECG. The Midmark IQecg Digital ECG system information is provided below. The total quantities manufactured and distributed noted below are the combined IQecgs Digital ECG and Midmark Digital ECG systems. Serial Numbers: 480000 4820704 UDI-DI: 00841709100581, 00841709100321, 00841709100895, 00841709100901

Recalling firm:

Midmark Corporation

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

Recall #:

99404

Lot/product code:

Lot Code: This correction affects IQecg plugin software versions starting with v10 and prior to v10.1.0.18 installed on Midmark Digital ECG. The Midmark Digital ECG system information is provided below. The total quantities manufactured and distributed noted below are the combined IQecgs Digital ECG and Midmark Digital ECG systems. Serial Numbers: 7817519 7817645, L1130587 V2967564 UDI-DI: 00841709121319, 08056732652491

Recalling firm:

Midmark Corporation

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

Recall #:

99322

Lot/product code:

UDI:9336472005542; Serial Numbers 0003-1533

Recalling firm:

SDI Limited

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

Recall #:

99476

Lot/product code:

All Serial Numbers/UDI: 00850005470342 Software Version: Paragonix App Ver. 6.1.1/6.1.2

Recalling firm:

Paragonix Technologies Inc.

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

Recall #:

99404

Lot/product code:

Lot Code: This correction affects IQecg plugin software versions starting with v10 and prior to v10.1.0.18 installed on Midmark IQecg Digital ECG. The Midmark IQecg Digital ECG system information is provided below. The total quantities manufactured and distributed noted below are the combined IQecgs Digital ECG and Midmark Digital ECG systems. Serial Numbers: 480000 4820704 UDI-DI: 00841709100581, 00841709100321, 00841709100895, 00841709100901

Recalling firm:

Midmark Corporation

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

Recall #:

99404

Lot/product code:

Lot Code: This correction affects IQecg plugin software versions starting with v10 and prior to v10.1.0.18 installed on Midmark Digital ECG. The Midmark Digital ECG system information is provided below. The total quantities manufactured and distributed noted below are the combined IQecgs Digital ECG and Midmark Digital ECG systems. Serial Numbers: 7817519 7817645, L1130587 V2967564 UDI-DI: 00841709121319, 08056732652491

Recalling firm:

Midmark Corporation

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

Recall #:

99561

Lot/product code:

UDI-DI 10198459362835 Lots 25IBJ918 25KBN677 25LBU066 26BBD775

Recalling firm:

Medline Industries, LP