Before you eat it, take it, or plug it in — check.

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

Recall #:

D-0628-2026

Lot/product code:

Lot AE01763, Expires 9/30/2027.

Recalling firm:

SUN PHARMACEUTICAL INDUSTRIES INC

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

Recall #:

99302

Lot/product code:

Lot Code: WebApp version 2.33.1, 2.33.3 and 2.34.2

Recalling firm:

Copan WASP

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

Recall #:

99109

Lot/product code:

Model Number: UHI-4. UDI: 04953170324147, 04953170467219. All Serial Numbers.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

99228

Lot/product code:

Model/UDI-DI: MMT-8600/00199150038978(10)1.1.0, MMT-8601/00199150038985(10)1.1.0 Software Versions: 1.0.0, 1.1.0

Recalling firm:

Medtronic MiniMed, Inc.

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

Recall #:

99083

Lot/product code:

ALL Cyberknife systems running software version 11.X and higher that utilize the Exchange Table.

Recalling firm:

Accuray Incorporated

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

Recall #:

99075

Lot/product code:

All systems prior with software version 11X that utilize the Exchange Table

Recalling firm:

Accuray Incorporated

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

Recall #:

D-0609-2026

Lot/product code:

Lots: N02327, expires: 09/2026; N02740, expires: 12/2026; N03069, expires: 08/2027.

Recalling firm:

The Harvard Drug Group LLC

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

Recall #:

99264

Lot/product code:

60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 Lot Number: 26025260 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 Lot Number: 26035455 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Lot Number: 26055528

Recalling firm:

BD SWITZERLAND SARL

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO2075; UDI-DI ¿03760279380100; Lot Number 250700016, 251000048, 251000049, and 260300043

Recalling firm:

TISSIUM SA

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

Recall #:

H-1125-2026

Lot/product code:

Lot: 260562 BB: 022527

Recalling firm:

Western Mixers Produce & Nuts, Inc.

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO1510; UDI-DI 03760279380070; Lot Numbers 250700041 and 251000032

Recalling firm:

TISSIUM SA

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO5010; UDI-DI 03760279380179; Lot Numbers 250700050, 251000043, 260300048, 260300049, and 260300050

Recalling firm:

TISSIUM SA

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

Recall #:

99284

Lot/product code:

REF: 1000035; Single Unit UDI: 5030267049844; Case UDI: 05030267044528; Lot No. 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565.

Recalling firm:

Intersurgical Inc

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO4010; UDI-DI 03760279380148; Lot Numbers 251000041, 250700048, 260300046, 260400050, and 260300047

Recalling firm:

TISSIUM SA

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO3010; UDI-DI 03760279380117; Lot Numbers 250700045, 251000040, 251000036, 251000037, 251000039, 251000035, and 251000064

Recalling firm:

TISSIUM SA

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO6010; UDI-DI ¿03760279380209; Lot Numbers 250700051, 251000044, and 251000045

Recalling firm:

TISSIUM SA

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

Recall #:

99333

Lot/product code:

REF/UDI-DI/Lot(Expiration): 384539/00886333209934/11488167(7/14/2026), 11488168(7/17/2026), 11494535E(8/1/2026), 11507766(11/13/2026), 11550780(12/12/2026), 11551487(12/15/2026), 11551488(12/15/2026); 384464/00886333209835/11490593(7/28/2026), 11494886(8/28/2026)11501150(10/6/2026); 384516/00886333209910/11500410(8/14/2026), 11501856(8/14/2026), 11504222(9/9/2026), 11506952(9/9/2026), 11523868(9/18/2026), 11551789(9/18/2026), 11553909(11/13/2026), 11559226(11/20/2026); 384463/00886333209828/11490797(8/1/2026), 11490959(8/11/2026)

Recalling firm:

Argon Medical Devices, Inc

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO2010; UDI-DI 03760279380094; Lot Number 250700042, 251000033, and 251000034

Recalling firm:

TISSIUM SA

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

Recall #:

99345

Lot/product code:

Lot Code: Model No NCOCO1575; UDI-DI ¿03760279380087; Lot Number 250700007, 251000031, and 260300041

Recalling firm:

TISSIUM SA

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

Recall #:

99333

Lot/product code:

REF/UDI-DI/Lot(Expiration): 384620/00886333210008/11490543(7/28/2026)

Recalling firm:

Argon Medical Devices, Inc

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

Recall #:

99285

Lot/product code:

Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.

Recalling firm:

Terumo Medical Corporation

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

Recall #:

99284

Lot/product code:

REF: 1100050; Single Unit UDI: 5030267050185; Case UDI: 05030267044450; Lot No. 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154.

Recalling firm:

Intersurgical Inc

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

Recall #:

H-1137-2026

Lot/product code:

Recalled Lot Codes - 408125075E14F2 - 708125076E14F2 - 708125083E14F2 - 408125139E14F2 - 708125141E14F2 - 708125145E14F2 - 708125174E14F2 - 709125273E14F2 - 709125280E14F2 - 709125288E14F2 - 409125307E14F2 - 70926019ENNB - 70926029ENNB - 70926035ENNB - 70926039ENNB - 70926042ENNB Use-By dates span March 16, 2027 - February 11, 2028

Recalling firm:

NARA ORGANICS INC

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

Recall #:

99210

Lot/product code:

UDI-DI: 14560189210032; Lot Numbers: FX12404, FY12407, FY12406, FZ12408

Recalling firm:

Tosoh Bioscience Inc

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

Recall #:

99334

Lot/product code:

1) DYKM1636A, UDI-DI: 10889942925858(each), 40889942925859(case), Lot Number: 25ABW688; 2) DYKM1636A, UDI-DI: 10889942925858(each), 40889942925859(case), Lot Number: 23LBT438; 3) DYKM1881A, UDI-DI: 10198459025174(each), 40198459025175(case), Lot Number: 24KBS611; 4) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 25BBB106; 5) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24KBJ751; 6) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24LBO630; 7) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24ABB622; 8) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24CBG290; 9) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24CBG291; 10) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24CBT163; 11) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24EBM679; 12) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24FBL963; 13) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24HBV589; 14) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24HBV590; 15) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24HBV591; 16) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24HBV592; 17) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24HBV593; 18) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24JBV697; 19) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24JBV698; 20) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 24JBV699; 21) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 23IBT699; 22) DYNDB3077C, UDI-DI: 10193489273809(each), 40193489273800(case), Lot Number: 23JBS210

Recalling firm:

Medline Industries, LP