Recalls affecting Guam

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 #:

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 #:

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

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-0780-2026

Lot/product code:

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

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-0786-2026

Lot/product code:

Lot #: D2402337, Exp. Date 10/31/2026.

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-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.

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.

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-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-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.

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

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-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 #:

99596

Lot/product code:

114093-000 - UDI-DI: 00857534006356, Serial Numbers: 10005695, 10002998, 10002997, 10005456, 10005612, 10004372, 10005613, 10002841, 10011119; 114093-600 - UDI-DI: 00857534006462, Serial Numbers: 10002996, 10004515, 10007411, 10007376

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-0783-2026

Lot/product code:

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

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-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-0777-2026

Lot/product code:

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

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-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.

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-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-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 #:

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