Recalls affecting Guam

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

Recall #:

D-0746-2026

Lot/product code:

Lot AV5913C, Expiry: 6/2027

Recalling firm:

Novartis Pharmaceuticals Corporation

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

Recall #:

99550

Lot/product code:

Lot Code: Model No 456025, UDI-DI 04046964183638, Lot Numbers 0062062778 and 0062062779

Recalling firm:

B Braun Medical Inc

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

Recall #:

D-0788-2026

Lot/product code:

Lot #: 6402820, Exp. Date 12/2028

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

99222

Lot/product code:

Model Number: INFX-8000C/B3 UDI code: Pending SID Number:30101165 Serial Number: B3E2422005 Model Number: INFX-8000F/SG UDI code: Pending SID Number: 30093711 Serial Number: SGC2412001 Model Number: INFX-8000V/SZ UDI code: Pending SID Number: 30029686 Serial Number: SZA2422001 SID Number: 79000002 Serial Number:SZA2442004 Model Number: INFX-8000V/SX UDI code: Pending SID Number: 30049491 Serial Number: SXA2432001 SID Number: 30100053 Serial Number: SXA2432002 Model Number: INFX-8000V/B9 UDI code: Pending SID Number: 30059175 Serial Number: B9F2412001 Model Number: INFX-8000V/ST UDI code: Pending SID Number: 30059180 Serial Number: STA2412001 Model Number: INFX-8000V/SZ UDI code: Pending SID Number: 30095017 Serial Number: SZA2432003 SID Number: 30097052 Serial Number: SZA2422002

Recalling firm:

Canon Medical System, USA, INC.

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

Recall #:

D-0761-2026

Lot/product code:

Batch TLF2506001, Date of Expiry: May 31, 2028.

Recalling firm:

Shoolin Pharma Chem LLP

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

Recall #:

D-0760-2026

Lot/product code:

Lot: TLF2506001, Date of Expiry: May 31, 2028.

Recalling firm:

Shoolin Pharma Chem LLP

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

Recall #:

D-0759-2026

Lot/product code:

Batch SDC2505001, Date of Expiry: April 30, 2030.

Recalling firm:

Shoolin Pharma Chem LLP

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

Recall #:

D-0762-2026

Lot/product code:

Batch TLF2506001, Date of Expiry: May 31, 2028.

Recalling firm:

Shoolin Pharma Chem LLP

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

Recall #:

D-0763-2026

Lot/product code:

Lot: SDC2505001, Date of Expiry: April 30, 2030.

Recalling firm:

Shoolin Pharma Chem LLP

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

Recall #:

D-0770-2026

Lot/product code:

Lot # AD94033, Exp Date: 5/31/2028.

Recalling firm:

SUN PHARMACEUTICAL INDUSTRIES INC

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

Recall #:

D-0789-2026

Lot/product code:

Lot#: KB00427, Exp date 4/30/2028; KA00308, Exp date 10/31/2026

Recalling firm:

Lupin Pharmaceuticals Inc.

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

Recall #:

99496

Lot/product code:

REF/UDI-DI/Lot: 10300012/5050474755093/UA32232, UA32250, UA32268, UA32290, UA32292, UA32303, UA32371, UP31203, UP31205; 10300016/5050474755116/UA32447, UA32448, UA32449, UB33008, UB33026, UB33082, UB33083, UB33175; 10301012/5050474755109/UB33014, UB33041, UB33057, UB33060, UB33100, UB33190; 10301016/5050474755123/UB33084, UB33194

Recalling firm:

Johnson & Johnson Surgical Vision, Inc.

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

Recall #:

D-0773-2026

Lot/product code:

Lot # 25ZF3670, Exp Date: May 31, 2027.

Recalling firm:

Liebel-Flarsheim Company LLC

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

Recall #:

99496

Lot/product code:

REF/UDI-DI/Lot: 10300012/5050474755093/UA32232, UA32250, UA32268, UA32290, UA32292, UA32303, UA32371, UP31203, UP31205; 10300016/5050474755116/UA32447, UA32448, UA32449, UB33008, UB33026, UB33082, UB33083, UB33175; 10301012/5050474755109/UB33014, UB33041, UB33057, UB33060, UB33100, UB33190; 10301016/5050474755123/UB33084, UB33194

Recalling firm:

Johnson & Johnson Surgical Vision, Inc.

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

Recall #:

D-0768-2026

Lot/product code:

Lot #: 2411550, Exp. 2026/NOV.

Recalling firm:

Heritage Pharmaceuticals Inc

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

Recall #:

99531

Lot/product code:

UDI : (01)3607450007466(11)250331(17)270331(10)273074(241)00746, Exp 3/31/2027

Recalling firm:

Diagnostica Stago, Inc.

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

Recall #:

99553

Lot/product code:

1) PBCGRGB28, UDI-DI: 10198956432567(each), 50198956432565(case), Lot Number: GKU1823 ; 2) PBVMLP22G, UDI-DI: 10198956123854(each), 50198956123852(case), Lot Number: NGKU2052 ; 3) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case), Lot Number: NGKU0856 ; 4) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case), Lot Number: NGKU0957 ; 5) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case), Lot Number: NGKU0856 ; 6) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case), Lot Number: NGKU0957 ; 7) PBV2MJMVH, UDI-DI: 10198956285248(each), 50198956285246(case), Lot Number: NGKV3390 ; 8) PB13GYAJD, UDI-DI: 10198956125193(each), 50198956125191(case), Lot Number: NGKV3390 ; 9) PB43LSEJG, UDI-DI: 10198956200999(each), 50198956200997(case), Lot Number: NGKW2883 ; 10) SMACGGRACE, UDI-DI: 10197106820506(each), 50197106820504(case), Lot Number: NGKU0856 ; 11) SMACGGRACE, UDI-DI: 10197106820506(each), 50197106820504(case), Lot Number: NGKU2052 ; 12) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case), Lot Number: NGKW0682 ; 13) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case), Lot Number: NGKW3769 ; 14) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case), Lot Number: NGKW3769 ; 15) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case), Lot Number: NGKW3769 ; 16) SMAVPDWTMC, UDI-DI: 10197106678053(each), 50197106678051(case), Lot Number: GKU1823 ; 17) SMAVPDWTMC, UDI-DI: 10197106678053(each), 50197106678051(case), Lot Number: GKU1823 ; 18) SMA4JGRODB, UDI-DI: 10197106670545(each), 50197106670543(case), Lot Number: NGKU0129 ; 19) SMA4JGRODB, UDI-DI: 10197106670545(each), 50197106670543(case), Lot Number: NGKU0129 ; 20) SMA4JLGODA, UDI-DI: 10197106674949(each), 50197106674947(case), Lot Number: NGKU0129 ; 21) SMA4JLGODA, UDI-DI: 10197106674949(each), 50197106674947(case), Lot Number: NGKU0129

Recalling firm:

Cardinal Health 200, LLC

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

Recall #:

99553

Lot/product code:

1) POV2SCCPP, UDI-DI: 10198956285200(each), 50198956285208(case), Lot Number: NGKV3390 ; 2) PWVMFFABLI, UDI-DI: 10198956123915(each), 50198956123913(case), Lot Number: NGKT2394

Recalling firm:

Cardinal Health 200, LLC

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

Recall #:

D-0766-2026

Lot/product code:

Lot 2552A, Exp 09/30/2027

Recalling firm:

Prestige Brands Holdings

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

Recall #:

D-0764-2026

Lot/product code:

Lot: P400172; Lot PA00050A, Exp 09/30/2027

Recalling firm:

Shilpa Medicare Limited

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

Recall #:

D-0756-2026

Lot/product code:

Lot: AC-017274, Exp. 12/12/2026.

Recalling firm:

Apollo Care, LLC

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

Recall #:

D-0757-2026

Lot/product code:

Lot: AC-017275, Exp. 12/13/2026; AC-017282, AC-017285, Exp. 12/27/2026.

Recalling firm:

Apollo Care, LLC

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

Recall #:

D-0747-2026

Lot/product code:

Lot: AC-017108, Exp. 11/17/2026; AC-017110, Exp. 11/20/2026; AC-017112, Exp. 11/21/2026; AC-017142, AC-017144, Exp. 12/10/2026; AC-017166, AC-017167, AC-017177, AC-017213, AC-017224, AC-017225, Exp. 12/31/2026

Recalling firm:

Apollo Care, LLC

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

Recall #:

D-0752-2026

Lot/product code:

Lot: AC-017131, Exp. 8/30/2026.

Recalling firm:

Apollo Care, LLC

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

Recall #:

99553

Lot/product code:

1) PEVMETBJX, UDI-DI: 10198956176041(each), 50198956176049(case), Lot Number: NGKT2394 ; 2) PEVMETBJX, UDI-DI: 10198956176041(each), 50198956176049(case), Lot Number: NGKT2394 ; 3) PEVMETB37, UDI-DI: 10198956212039(each), 50198956212037(case), Lot Number: NGKT2394

Recalling firm:

Cardinal Health 200, LLC