Recalls affecting U.S. Virgin Islands

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

Recall #:

99784

Lot/product code:

UDI:N/A

Recalling firm:

Philips North America Llc

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

Recall #:

99784

Lot/product code:

UDI for Brilliance iCT: (01)00884838059474, UDI for Brilliance iCT Upgrades: N/A, UDI for Brilliance iCT SP: N/A.

Recalling firm:

Philips North America Llc

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

Recall #:

D-0771-2026

Lot/product code:

Lot #: a) GS067429, GS068091, Exp 5/31/2028; b) GS067430, GS068090, Exp 5/31/2028

Recalling firm:

Golden State Medical Supply Inc.

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

Recall #:

99784

Lot/product code:

UDI:N/A

Recalling firm:

Philips North America Llc

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

Recall #:

99784

Lot/product code:

UDI: Ingenuity CT Upgrades (01)00884838098701, Ingenuity CT China (01)00884838059863, Ingenuity Core 128 Elite Brazil: N/A

Recalling firm:

Philips North America Llc

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

Recall #:

99784

Lot/product code:

UDI for Brilliance iCT: (01)00884838059474, UDI for Brilliance iCT Upgrades: N/A, UDI for Brilliance iCT SP: N/A.

Recalling firm:

Philips North America Llc

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

Recall #:

99680

Lot/product code:

1. Model Number(Size): 8124(24FR); UDI-DI: 00650862132243; Lot Number: ME244852; 2. Model Number(Size): 8128(28FR); UDI-DI: 00650862132281; Lot Number: ME244854, ME244855; 3. Model Number(Size): 8132(32FR); UDI-DI: 00650862132328; Lot Numbers: ME244565, ME244858, ME244859; 4. Model Number(Size): 8136(36FR); UDI-DI: 00650862132366; Lot Number: ME244861;

Recalling firm:

Atrium Medical Corporation

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

Recall #:

99784

Lot/product code:

UDI: Ingenuity CT Upgrades (01)00884838098701, Ingenuity CT China (01)00884838059863, Ingenuity Core 128 Elite Brazil: N/A

Recalling firm:

Philips North America Llc

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

Recall #:

99680

Lot/product code:

1. Model Number(Size): 15028(28FR); UDI-DI: 00650862150285; Lot Number: ME244891; 3. Model Number(Size): 15036(36FR); UDI-DI: 00650862150360; Lot Number: ME244850;

Recalling firm:

Atrium Medical Corporation

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

Recall #:

99524

Lot/product code:

UDI-DI: 00802526613838

Recalling firm:

Boston Scientific Corporation

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

Recall #:

D-0777-2026

Lot/product code:

Lot #: D2402016, D2402017, Exp. Date 08/31/2026

Recalling firm:

ACCORD HEALTHCARE, INC.

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

Recall #:

99524

Lot/product code:

UDI-DI: 00802526613883

Recalling firm:

Boston Scientific Corporation

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

Recall #:

D-0803-2026

Lot/product code:

Lot#: NDC 63004-8710-1 - 1564-107, exp 1/31/2027 NDC 63004-8710-2 - 1564-107H, exp 1/31/2027

Recalling firm:

Mallinckrodt Hospital Products Inc.

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

Recall #:

D-0779-2026

Lot/product code:

a) Lot #: D2402186, Exp. Date 09/30/2026. b) Lot #: D2402019, Exp. Date 08/31/2026; D2402094, Exp. Date 09/30/2026; D2500022, D2500023, D2500021, Exp. Date 12/31/2026.

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-0784-2026

Lot/product code:

a) Lot #: D2402642, Exp. Date 11/30/2026 b) Lot #: D2401832, Exp. Date 08/31/2026; D2402525, D2402527, D2402526, D2402644, D2402643, Exp. Date 11/30/2026.

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-0778-2026

Lot/product code:

Lot #: D2401813, D2401814, Exp. Date 08/31/2026; D2500200, D2500219, Exp. Date 12/31/2026.

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-0785-2026

Lot/product code:

a) Lot # D2402430, D2402431, Exp Date: 10/31/2026. b) Lot #: D2402432, Exp. Date 10/31/2026; D2500180, Exp. Date 12/31/2026.

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-0782-2026

Lot/product code:

a) Lot # D2402125, D2402126, D2402127, Exp. Date 09/30/2026. b) Lot #: D2402523, D2402524, Exp. Date 11/30/2026.

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-0783-2026

Lot/product code:

Lot #: D2402195, D2402196, D2402197, Exp. Date 09/30/2026.

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-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 #:

99596

Lot/product code:

113821-600 - Serial Numbers: 10003754, 10006997; 114148-000 - UDI-DI: 00857534006349, Serial Numbers: 10005189, 10005190, 10004463, 10004997

Recalling firm:

IMRIS Imaging Inc

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

Recall #:

D-0776-2026

Lot/product code:

Lot #: D2401834, D2401982, Exp. Date 08/31/2026; D2402584, D2402585, D2402586, D2402588, D2402587, D2402589, Exp Date. 11/30/2026.

Recalling firm:

ACCORD HEALTHCARE, INC.

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

Recall #:

99524

Lot/product code:

UDI-DI: 00802526613852

Recalling firm:

Boston Scientific Corporation

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

Recall #:

D-0781-2026

Lot/product code:

Lot #: D2401983, Exp. Date 08/31/2026; D2402640, D2402641, Exp. Date 11/30/2026; D2500224, Exp. Date 01/31/2027.

Recalling firm:

ACCORD HEALTHCARE, INC.