Recalls affecting Guam

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

Recall #:

D-0831-2026

Lot/product code:

a) Lot #: AC5470A, Exp. Date July 2027 b) Lot #: AC5470B, Exp. Date July 2027

Recalling firm:

Hikma Pharmaceuticals USA INC.

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

Recall #:

99607

Lot/product code:

Model Number: PS-0523CJDA. UDI-DI: 00821925044531. Lot Number: FR490902.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

99607

Lot/product code:

Model Number: PS-0523CJDA. UDI-DI: 00821925044531. Lot Number: FR490902.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

D-0804-2026

Lot/product code:

Lot # TY9494, Exp Date: 05/31/2027.

Recalling firm:

Apotex Corp.

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

Recall #:

D-0832-2026

Lot/product code:

Lot#: J4H077, Exp 30NOV2026.

Recalling firm:

B BRAUN MEDICAL INC

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

Recall #:

99557

Lot/product code:

UDI-DI 05413765852428, all serial numbers

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

99557

Lot/product code:

UDI-DI 00197886002300, all serial numbers

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

99556

Lot/product code:

Lots 25JR01801 25KR01225 25KR01251 25NR01016 25NR01265 UDI-DI 00840861102532

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

99556

Lot/product code:

Lots 25JR01800 25KR01224 25LR01001 25NR01018 25NR01272 25PR01077 25PR01219 25PR01220 UDI-DI 00840861102518

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

99556

Lot/product code:

Lots 25KR01227 25NR01257 UDI-DI 00840861102556

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

99556

Lot/product code:

Lots 25JR01800 25KR01224 25LR01001 25NR01018 25NR01272 25PR01077 25PR01219 25PR01220 UDI-DI 00840861102518

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

99556

Lot/product code:

Lots 25JR01802 25NR01017 25NR01266 UDI-DI 00840861102525

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

99556

Lot/product code:

Lots 25JR01801 25KR01225 25KR01251 25NR01016 25NR01265 UDI-DI 00840861102532

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

D-0790-2026

Lot/product code:

Lot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028.

Recalling firm:

Church & Dwight Co., Inc.

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

Recall #:

99556

Lot/product code:

Lots 25KR01227 25NR01257 UDI-DI 00840861102556

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

99556

Lot/product code:

Lots 25JR01802 25NR01017 25NR01266 UDI-DI 00840861102525

Recalling firm:

Fresenius Medical Care Renal Therapies Group, LLC

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

Recall #:

D-0827-2026

Lot/product code:

Lot: 16UI07, Exp 08/31/2028

Recalling firm:

Fresenius Kabi USA, 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: 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: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): 8016(16FR); UDI-DI: 00650862130164; Lot Number: ME244878; 2. Model Number(Size): 8024(24FR); UDI-DI: 00650862130249; Lot Number: ME244835; 3. Model Number(Size): 8028(28FR); UDI-DI: 00650862130287; Lot Numbers: ME244682, ME244836, ME244837, ME244681; 4. Model Number(Size): 8032(32FR); UDI-DI: 00650862130324; Lot Number: ME244840; 5. Model Number(Size): 8036(36FR); UDI-DI: 00650862130362; Lot Number: ME244686;

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): 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

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