Recalls affecting Virginia

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

Recall #:

98618

Lot/product code:

Product code:ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25K0130

Recalling firm:

ARROW INTERNATIONAL, LLC

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

Recall #:

98618

Lot/product code:

Product Code: ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 Batch Number: 33F25M0671

Recalling firm:

ARROW INTERNATIONAL, LLC

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

Recall #:

98618

Lot/product code:

Product Code: ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531(11)251205(10)33F25M0011 Batch Number: 33F25M0011 Product Code: ASK-45703-MGH UDI code: (01)10801902223675(17)261231(11)251209(10)33F25L0143 Batch Number: 33F25L0143 Product Code: ASK-42854-MGH UDI code: (01)10801902223668(17)261231(11)251210(10)33F25L0144 Batch Number: 33F25L0144 Product Code: ASK-45854-MGH UDI code: (01)10801902223699(17)261231(11)251209(10)33F25L0145 Batch Number: 33F25L0145

Recalling firm:

ARROW INTERNATIONAL, LLC

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

Recall #:

98618

Lot/product code:

Product code: ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Batch Number: 33F25J0347

Recalling firm:

ARROW INTERNATIONAL, LLC

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

Recall #:

98659

Lot/product code:

UDI-DI: B098AMS144330; Lot Numbers: 204612 206723 210211 213641 216064 222060 224073 225012 236012 236910

Recalling firm:

Windstone Medical Packaging, Inc.

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

Recall #:

D-0434-2026

Lot/product code:

Batch# 24EU10010, Exp Date: 05/31/2027.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0429-2026

Lot/product code:

Batch# 6402428, Exp Date: 10/31/2026; Batch# 6402481, 6402482, Exp Date: 11/30/2026.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0430-2026

Lot/product code:

Batch# 6402153, Exp Date: 11/30/2026; Batch# 6402297, 6402298, Exp Date: 01/31/2027; Batch# 6402377, 6402378, 6402379, Exp Date: 02/28/2027; Batch # 6402429, 6402430, 6402431, 6402432, 6402433, Exp Date: 03/31/2027; Batch# 6402434, Exp Date: 04/30/2027; Batch# 6402512, Exp Date: 05/2027; Batch# 6402574, 6402576, Exp Date: 06/30/2027.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

98659

Lot/product code:

UDI-DI: B098AMS14994A0; Lot Numbers: 224792 228566 230105 230853 234209

Recalling firm:

Windstone Medical Packaging, Inc.

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

Recall #:

D-0424-2026

Lot/product code:

Batch # 6402413, Exp Date: 02/29/2028

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0431-2026

Lot/product code:

Batch# 6402290, 6402291, Exp Date: 01/31/2028; Batch# 6402411, Exp Date: 02/29/2028; Batch# 6402412, 6402419, 6402424, 6402425, 6402426, 6402427, Exp Date: 03/31/2028; Batch# 6402479, 6402480, 6402517, 6402571, Exp Date: 05/31/2028; Batch# 6402518, Exp Date: 06/30/2028.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0427-2026

Lot/product code:

Batch# 23SU10008, Exp Date: 12/31/2026; Batch# 24JU10003, Exp Date: 07/31/2027; Batch# 24LU10011, 24LU10012, Exp Date: 9/30/2027; Batch# 6402273, 6402275, Exp Date: 01/31/2028; Batch# 6402420, 6402421, 6402422, 6402423, Exp Date: 03/31/2028; Batch# 6402473, 6402474, 6402475, 6402476, 6402485, Exp Date: 04/30/2028; Batch# 6402516, Exp Date: 05/31/2028.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0437-2026

Lot/product code:

Batch# 6402165, Exp Date: 05/30/2028.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0435-2026

Lot/product code:

Batch# 6402296, Exp Date: 07/31/2026.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0426-2026

Lot/product code:

Batch# 6402299, 6402300, 6402301, 6402302, 6402303, Exp Date: 01/31/2027; Batch# 6402305, 6402398, Exp Date: 02/28/2027; Batch# 6402467, Exp Date: 04/30/2027; Batch# 6402577, 6402578, Exp Date: 06/30/2027.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

98525

Lot/product code:

UDI:00886874121931/All serial Numbers

Recalling firm:

Intuitive Surgical, Inc.

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

Recall #:

H-0640-2026

Lot/product code:

NFDM Low Heat, NFDM High Heat, and SMP Medium Heat Lot Codes : 26015B; 26016B; 26017B; 26018B; 26019B; 26022B; 26023B; 26024B; 26024BT; 26025B; 26025BT; 26026B; 26027B; 26028B; 26029B; 26030B; 26034B; 26035B; 26040B; 26041B; 26041BT; 26042B; 26042BT; 26043B; 26044B; 26046BT; 26047BT; 26048BT. The products were packaged in 25 kg bags or 1 metric ton totes.

Recalling firm:

Lone Star Dairy Products LLC

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

Recall #:

98659

Lot/product code:

UDI-DI: B098AMS149940; Lot Numbers: 220039 221423 224226 224793 225009

Recalling firm:

Windstone Medical Packaging, Inc.

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

Recall #:

98653

Lot/product code:

US: Basic UDI Number 0763000B000262284, GTIN: 00763000871741; 00763000973391; 00763000973506; 00763000993269; 00199150003709. OUS: 00763000871734; 00763000973384; 00763000973513; 00763000811341; 00763000911515; 00763000963675; 00199150003716. 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Recalling firm:

Medtronic, Inc.

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

Recall #:

D-0432-2026

Lot/product code:

Batch# 23DU10004, Exp Date: 04/30/2026; Batch# 23HU10006, Exp Date: 06/30/2026.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0433-2026

Lot/product code:

Batch# 23SU10001, Exp Date: 12/31/2026; Batch# 24AU10003, 24AU10004, 24AU10005, 24AU10008, Exp Date: 01/31/2027; Batch # 24EU10001, 24EU10002, Exp Date: 05/31/2027; Batch# 24PU10002, Exp Date: 11/30/2027; Batch# 25BU10003, Exp Date: 02/29/2028; Batch# 25EU10005, Exp Date: 05/31/2028.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0425-2026

Lot/product code:

Batch# 6402372, 6402374, Exp Date: 08/31/2026; Batch# 6402437, Exp Date: 10/31/2026.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0436-2026

Lot/product code:

Batch# 6402399, 6402400, 6402401, Exp Date: 02/28/2027.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

D-0428-2026

Lot/product code:

Batch# 24LU10013, 24LU10014, Exp Date: 09/30/2027; Batch# 24NU10001, 24NU10002, Exp Date: 10/31/2027.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

98675

Lot/product code:

ARTIS pheno UDI: 4056869046877. ARTIS icono biplane UDI: 4056869063317. ARTIS icono ceiling UDI: 4056869295923. ARTIS icono floor UDI: 4056869149325.

Recalling firm:

Siemens Medical Solutions USA, Inc