Recalls affecting Guam

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.

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

Recall #:

D-0774-2026

Lot/product code:

Lot# 3227809; Expiry:10/2026; NDC #: 0378-6333-80

Recalling firm:

Mylan Pharmaceuticals Inc

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.

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

Recall #:

99631

Lot/product code:

All serial numbers.

Recalling firm:

Spectral Instruments 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-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 #:

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-0802-2026

Lot/product code:

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

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-0794-2026

Lot/product code:

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

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

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.

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-0797-2026

Lot/product code:

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

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-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

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

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 #:

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 10889942925858 Lot 26EBI940

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:

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