Recalls affecting Northern Mariana Islands

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

Recall #:

99631

Lot/product code:

All serial numbers.

Recalling firm:

Spectral Instruments 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.

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

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 #:

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-0795-2026

Lot/product code:

Lot #: 24353, Exp. Date: 9/30/2026.

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-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-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 #:

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-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 #:

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-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-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-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

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 #:

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 #:

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

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

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 #:

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 #:

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:

DYKS1583A UDI-DI 10198459146640 Lot 24KBP388

Recalling firm:

Medline Industries, LP