Recalls affecting American Samoa

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

Recall #:

D-0793-2026

Lot/product code:

Lot #: 25082, Exp. Date: 3/31/2027.

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0796-2026

Lot/product code:

Lot #: 24418, Exp. Date: 11/30/2026; 25131, Exp. Date: 3/31/2027; 25349, Exp. Date: 8/31/2027

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0802-2026

Lot/product code:

Lot #: 25295N0C0, Exp. Date: 04/30/2027.

Recalling firm:

American Regent, Inc.

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

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

Recall #:

99631

Lot/product code:

All serial numbers.

Recalling firm:

Spectral Instruments Inc

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

Recall #:

D-0792-2026

Lot/product code:

Lot #: 24297, Exp. Date 8/31/2026; 24364, Exp. Date: 10/31/2026;

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0791-2026

Lot/product code:

Lot #: 24291, Exp. Date: 8/31/2026

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0797-2026

Lot/product code:

Lot #: 24426, Exp. Date: 11/30/2026; 25220, Exp. Date: 5/31/2027.

Recalling firm:

American Regent, Inc.

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

Recall #:

Lot/product code:

Lot # LD175708, Exp Date: 14-Feb-2027.

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

D-0800-2026

Lot/product code:

Lot #: 25202, Exp. Date: 11/30/2026.

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0798-2026

Lot/product code:

Lot #: 25090, Exp. Date 2/28/2027.

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0794-2026

Lot/product code:

Lot #: 24299, Exp. Date: 8/31/2026.

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0799-2026

Lot/product code:

Lot #: 25163, Exp. Date: 4/30/2027.

Recalling firm:

American Regent, Inc.

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

Recall #:

D-0787-2026

Lot/product code:

Lot # LD175708, Exp Date: 14-Feb-2027.

Recalling firm:

Baxter Healthcare Corporation

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-0733-2026

Lot/product code:

Batch # DMC125018A, Exp Date: 07/2027.

Recalling firm:

Aurobindo Pharma USA Inc

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

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

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

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

Recall #:

H-1242-2026

Lot/product code:

No lot code information. Recall is for all product with a pack date of 07/01/2026 through 07/31/2026

Recalling firm:

Coast Citrus Distributors

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 10198459362835 Lots 25IBJ918 25KBN677 25LBU066 26BBD775

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:

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

Recalling firm:

Medline Industries, LP