Recalls affecting U.S. Virgin Islands

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

Recall #:

D-0780-2026

Lot/product code:

Lot #: D2402443, D2402444, D2402445, Exp. Date 10/31/2026.

Recalling firm:

ACCORD HEALTHCARE, INC.

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

Recall #:

99601

Lot/product code:

Lot Code: Model: DermaV Software Version: 1.06 UDI #: 08800291820200 Serial Numbers: DV025A010, DV025A011, DV025A012, DV025A013, DV025A014, DV025A015 DV025A016, DV025A018, DV025A019, DV025A020, DV025A021, DV025A022, DV025B011, DV025B012, DV025B013, DV025B014, DV025B015, DV025D006, DV025D007, DV025D008, DV025D009, DV025D010, DV025E003, DV025E004, DV025E005, DV025E006, DV025E007, DV025E008, DV025E009, DV025E010, DV025E011, DV025E012, DV025E013, DV025E014, DV025E016, DV025E017, DV025F012, DV025F013, DV025F014, DV025F015, DV025F016, DV025G011, DV025G012, DV025G013, DV025G014, DV025G015, DV025G016, DV025G017, DV025G018, DV025G019, DV025G020, DV025J021, DV025J022, DV025J023, DV025J025, DV025J026, DV025J027, DV025J028, DV025J034, DV025J035, DV025J036, DV025J037, DV025J038, DV025J040, DV025K018, DV025K019, DV025K020, DV025K021, DV025K023, DV025K024, DV025K025, DV025K027, DV025M031, DV025M032, DV025M033, DV025M034, DV026B001, DV026B002, DV026B003, DV026B004, DV026B005, DV026B010, DV026B014, DV026B015, DV026B016, DV026B017, DV026B018, DV026C006, DV026C007, DV026C008, DV026C009, DV026C010, DV025M035

Recalling firm:

Lutronic Corporation

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

Recall #:

D-0775-2026

Lot/product code:

Lot #: D2401927, D2401833, Exp. Date 08/31/2026; D2402551, D2402552, Exp. Date 11/30/2026; D2500220, Exp. Date 12/31/2026; D2500223, Exp. Date 01/31/2027.

Recalling firm:

ACCORD HEALTHCARE, INC.

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

Recall #:

D-0745-2026

Lot/product code:

Lot # E408618, Expiry: 11/30/2026, NDC #: 70710-1159-3

Recalling firm:

Zydus Pharmaceuticals (USA) Inc

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

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 #:

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.

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.

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

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-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-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-0789-2026

Lot/product code:

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

Recalling firm:

Lupin Pharmaceuticals Inc.

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-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-0759-2026

Lot/product code:

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

Recalling firm:

Shoolin Pharma Chem LLP

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

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

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-0749-2026

Lot/product code:

Lot: C-017115, Exp. 11/25/2026; AC-017163, Exp. 12/31/2026; AC-017169, AC-017170, AC-017171, Exp. 12/31/2026; AC-017230, AC-017231, Exp. 5/5/2027.

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