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-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.

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

Recall #:

H-1267-2026

Lot/product code:

Batch code/ Best Before (bottom of package): LLA619603 31 OCT 2027 LLA619703 31 OCT 2027

Recalling firm:

Dreyer's Grand Ice Cream 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 #:

H-1264-2026

Lot/product code:

Batch code/ Best Before (bottom of package): LLA616903 30 SEP 2027 LLA617003 30 SEP 2027 LLA617103 30 SEP 2027 LLA617203 30 SEP 2027 LLA617303 30 SEP 2027 LLA617403 30 SEP 2027 LLA617503 30 SEP 2027 LLA617603 30 SEP 2027 LLA620303 31 OCT 2027 LLA620403 31 OCT 2027 LLA620503 31 OCT 2027 LLA620603 31 OCT 2027 LLA620703 31 OCT 2027 LLA620803 31 OCT 2027 LLA620903 31 OCT 2027 LLA621003 31 OCT 2027 LLA621103 31 OCT 2027 LLA621203 31 OCT 2027 LLA621303 30 NOV 2027 LLA621403 30 NOV 2027 LLA621503 30 NOV 2027 LLA621603 30 NOV 2027

Recalling firm:

Dreyer's Grand Ice Cream Inc.

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

Recall #:

H-1265-2026

Lot/product code:

Batch code/ Best Before (bottom of package): LLA617603 30 JUN 2027 LLA617703 30 JUN 2027 LLA617803 30 JUN 2027 LLA617903 30 JUN 2027 LLA618003 30 JUN 2027 LLA618103 30 JUN 2027 LLA618203 31 JUL 2027 LLA618303 31 JUL 2027 LLA618403 31 JUL 2027 LLA618503 31 JUL 2027 LLA619003 31 JUL 2027 LLA619103 31 JUL 2027 LLA619203 31 JUL 2027 LLA619303 31 JUL 2027 LLA619403 31 JUL 2027 LLA619503 31 JUL 2027

Recalling firm:

Dreyer's Grand Ice Cream Inc.

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

Recall #:

H-1268-2026

Lot/product code:

Batch code/ Best Before (bottom of package): LLA618503 31 JUL 2027 LLA618603 31 JUL 2027 LLA618703 31 JUL 2027 LLA618803 31 JUL 2027 LLA618903 31 JUL 2027 LLA619003 31 JUL 2027

Recalling firm:

Dreyer's Grand Ice Cream Inc.

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

Recall #:

H-1269-2026

Lot/product code:

Batch code/ Best Before (bottom of package: LLA603840 31 MAY 2027 LLA605540 31 MAY 2027 LLA605640 31 MAY 2027 LLA605740 31 MAY 2027 LLA605940 31 MAY 2027

Recalling firm:

Dreyer's Grand Ice Cream Inc.

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

Recall #:

H-1266-2026

Lot/product code:

Batch code/ Best Before (bottom of package): LLA616803 30 SEP 2027 LLA616903 30 SEP 2027 LLA619703 31 OCT 2027 UPC Bottom of package: 041548244044 LLA619803 31 OCT 2027 LLA619903 31 OCT 2027 LLA620003 31 OCT 2027 LLA620103 31 OCT 2027 LLA620203 31 OCT 2027 LLA620303 31 OCT 2027

Recalling firm:

Dreyer's Grand Ice Cream Inc.

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 00197886002300, 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 05413765852428, 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 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 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

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

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 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

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

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 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