Recalls affecting Arizona

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

D-0585-2026

Lot/product code:

Lot AM251676, EXP 11/31/2028

Recalling firm:

Amneal Pharmaceuticals, LLC

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

Recall #:

99148

Lot/product code:

UDI: 00815948024113/Lots: H00008699, H00008701, H00008702, H00008703, and C00020038

Recalling firm:

Penumbra, Inc.

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

Recall #:

D-0639-2026

Lot/product code:

Lot# 003, 004, 005, 006, 007, 008, 009, 010, 011, 012, 014, 015, 017, 018, 019, 020, 021, 022, 023, 024, 025, 026, 027, 028, 029, 030, 034, 035, 036, 037, 038, 039, 041, 042, 043, 044, 048, 049, 050, 051, 052, 053, 054, 055, 056, 057, 058, 059, 060, 061, 062, 063, 064, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

D-0636-2026

Lot/product code:

Lot# 001, 002, 003, 004, 005, 006, 010, 011, 012, 013, 014, 016, 017, 018, 019, 020, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

D-0632-2026

Lot/product code:

Lot# 0005, within expiry

Recalling firm:

Dabur India Limited

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

Recall #:

D-0637-2026

Lot/product code:

Lot# 022, 023 ,024, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

D-0635-2026

Lot/product code:

Lot# 007, 008, 009, 015, 016, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

H-1080-2026

Lot/product code:

Lot Code: 26020. Expiration: 06.12.28 UPC Codes: 6946976817911

Recalling firm:

Prime Food Processing LLC.

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

Recall #:

D-0638-2026

Lot/product code:

Lot# 001, 002, 003, 004, 005, 006, 007, 008, 009, 010, 011, 012, 013, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

D-0631-2026

Lot/product code:

Lot# 0001, and Lot# 0005, within expiry

Recalling firm:

Dabur India Limited

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

Recall #:

99259

Lot/product code:

UDI 00607567700406, Serial/Lot Number 3000547797

Recalling firm:

Maquet Cardiovascular, LLC

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

Recall #:

D-0641-2026

Lot/product code:

Lot# 011, 014, 015, 016, 017, 018, 019, 020, 021, 022, 026, Within Expiry.

Recalling firm:

Dabur India Limited

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

D-0619-2026

Lot/product code:

Lot S25133A

Recalling firm:

ANI Pharmaceuticals, Inc.

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

Recall #:

D-0640-2026

Lot/product code:

Lot# 001, 002, 013, 016, 031, 032, 033, 045, 046, 047, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

D-0642-2026

Lot/product code:

Lot# 001, 002, 003, 004, 005, 006, 007, 008, 009, 010, 012, 013, 023, 024, 025, 027, 028, 029, 031, 032, 033, 034, 035, Within Expiry.

Recalling firm:

Dabur India Limited

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

Recall #:

D-0630-2026

Lot/product code:

Lot# 0002, Lot# 0003, within expiry

Recalling firm:

Dabur India Limited

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

Recall #:

D-0633-2026

Lot/product code:

Lot# 0004, within expiry

Recalling firm:

Dabur India Limited

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

Recall #:

D-0634-2026

Lot/product code:

Lot# 0003, within expiry

Recalling firm:

Dabur India Limited

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

Recall #:

D-0629-2026

Lot/product code:

Lot# 0001, 0002, within expiry

Recalling firm:

Dabur India Limited

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

Recall #:

99069

Lot/product code:

REF/UDI-DI Box:Unit/Lot(Expiration): GUTS1000/20886333001594:00886333001590/11649760(3/31/2028)

Recalling firm:

Argon Medical Devices, Inc

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

D-0654-2026

Lot/product code:

Lot, expiry: Lot DNG0283A, exp 03/31/2027; Lots DNF0922A and DNF0923B, exp 10/31/2026

Recalling firm:

SUN PHARMACEUTICAL INDUSTRIES INC

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

D-0608-2026

Lot/product code:

Lot VA0099422; Exp. Date June 30, 2028

Recalling firm:

Sandoz Inc

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

Recall #:

99069

Lot/product code:

REF/UDI-DI Box:Unit/Lot(Expiration): CB0033TL/20886333217308:00886333217304/11650820(3/31/2028), 11652276(3/31/2028); CB0355TLA/20886333217698:00886333217694/11651977(3/31/2028);

Recalling firm:

Argon Medical Devices, Inc

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

Recall #:

99069

Lot/product code:

REF/UDI-DI Box:Unit/Lot(Expiration): 008416A/20886333217636:00886333217632/11656898(7/19/2027); 008566A/20886333217643:00886333217649/11654475(12/31/2026), 11654478(7/19/2027)

Recalling firm:

Argon Medical Devices, Inc

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

Recall #:

99069

Lot/product code:

REF/UDI-DI Box:Unit/Lot(Expiration): 400115A/20886333212884:00886333212880/11655174(7/19/2027), 11655183(7/19/2027), 11655185(7/19/2027), 11659131(7/19/2027);

Recalling firm:

Argon Medical Devices, Inc