Recalls affecting Delaware

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

Recall #:

98599

Lot/product code:

1) DYNJ32841F, UDI-DI: 10195327037796(each), 40195327037797(case), Lot Number: 24CBF407; 2) DYNJ46069D, UDI-DI: 10193489493184(each), 40193489493185(case), Lot Number: 24KBG704; 3) DYNJ51935A, UDI-DI: 10889942735549(each), 40889942735540(case), Lot Number: 24BME364; 4) DYNJ68902A, UDI-DI: 10193489870411(each), 40193489870412(case), Lot Number: 24BMC999; 5) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 22KBJ690; 6) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23BBD696; 7) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23DBG588; 8) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23FBD221; 9) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23GBN050; 10) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23IBB710; 11) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23LBM277; 12) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 24CBN011; 13) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 24DBK248; 14) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 24GBC694; 15) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 24HBX136; 16) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 24IBR538; 17) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 25ABC728; 18) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 25CBE147; 19) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 25CBP816; 20) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 23JBS196; 21) DYNJ80679A, UDI-DI: 10195327273705(each), 40195327273706(case), Lot Number: 25EBM284; 22) DYNJ82370A, UDI-DI: 10198459220227(each), 40198459220228(case), Lot Number: 25BBT096; 23) DYNJ82370A, UDI-DI: 10198459220227(each), 40198459220228(case), Lot Number: 25DBO043; 24) DYNJ84272, UDI-DI: 10195327349882(each), 40195327349883(case), Lot Number: 24KBE401; 25) DYNJ84272, UDI-DI: 10195327349882(each), 40195327349883(case), Lot Number: 25BBO542

Recalling firm:

Medline Industries, LP

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

Recall #:

98599

Lot/product code:

1) DYNJ59030B, UDI-DI: 10198459176920(each), 40198459176921(case), Lot Number: 24KBL574; 2) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 24IBJ666; 3) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 24JBM014; 4) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 24KBE220; 5) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 24LBJ174; 6) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 25ABW145; 7) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 25CBK525; 8) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 25EBA897; 9) DYNJ908586C, UDI-DI: 10198459058677(each), 40198459058678(case), Lot Number: 25GBK561; 10) VASC1081C, UDI-DI: 10195327054519(each), 40195327054510(case), Lot Number: 25FBA927

Recalling firm:

Medline Industries, LP

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

Recall #:

98599

Lot/product code:

1) DYNJ41648A, UDI-DI: 10198459062834(each), 40198459062835(case), Lot Number: 25CLA242; 2) DYNJ41648A, UDI-DI: 10198459062834(each), 40198459062835(case), Lot Number: 24LLA758

Recalling firm:

Medline Industries, LP

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

Recall #:

98599

Lot/product code:

1) DYNJ37543A, UDI-DI: 10193489919561(each), 40193489919562(case), Lot Number: 24DDA193

Recalling firm:

Medline Industries, LP

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

Recall #:

98454

Lot/product code:

Model: 3005PK; UDI: 00821925036000; Lot Numbers: All unexpired;

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98454

Lot/product code:

Model: 920005PK; UDI: 00821925036178; Lot Numbers: All unexpired;

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98454

Lot/product code:

Model: 920000PK; UDI: 00821925038080; Lot Numbers: All unexpired;

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98454

Lot/product code:

Model: 3006; UDI: 00821925035898; Lot Numbers: All unexpired;

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98454

Lot/product code:

Model: HACF0533; UDI: 00821925036390; Lot Numbers: All unexpired;

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-0399-2026

Lot/product code:

Lot #: 3116110, 3116130, Exp. Date 07/2026

Recalling firm:

MYLAN PHARMACEUTICALS INC

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

Recall #:

98498

Lot/product code:

Siemens Material Number (SMN): 11097536; UDI-DI: 00630414220505; Lot numbers: 150131, 150132, 150232, 150260, 150283, 150344, 150361, 150365, 150366, 150445, 150453, 150460, 150498, 150505, 150562, 150600, 150618, 150621;

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

98514

Lot/product code:

UDI: 07613327296167; All Lots

Recalling firm:

Stryker Communications

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

Recall #:

98442

Lot/product code:

Lot Code: See Excel sheet attached named "FDA 5072 Product Information" See Spreadsheet attached named "FDA 5072 Product Quantity Distributed" Catalog Number: 53430108 (ELEGANCE 1 LEVEL CERVICAL PLATE 8MM) UDI-DI code: 03700780644353 Lot Numbers: PC03X R879X Catalog Number: 53430110 (ELEGANCE 1 LEVEL CERVICAL PLATE 10MM) UDI-DI code: 03700780644353 Lot Numbers: P758X RAA2X R825X R902X Catalog Number: 53430111 (ELEGANCE 1 LEVEL CERVICAL PLATE 11MM) UDI-DI code: 03700780644384 Lot Numbers: R194X RAA1X Catalog Number: 53430112 (ELEGANCE 1 LEVEL CERVICAL PLATE 12MM) UDI-DI code: 03700780644391 Lot Numbers: R195X RAB2X Catalog Number: 53430113 (ELEGANCE 1 LEVEL CERVICAL PLATE 13MM) UDI-DI code: 03700780644407 Lot Numbers: R196X R197X R584X RA81X Catalog Number: 53430114 (ELEGANCE 1 LEVEL CERVICAL PLATE 14MM) UDI-DI code: 03700780644414 Lot Number: R585X Catalog Number: 53430116 (ELEGANCE 1 LEVEL CERVICAL PLATE 16MM) UDI-DI code: 03700780644438 Lot Number: R586X Catalog Number: 53430120 (ELEGANCE 1 LEVEL CERVICAL PLATE 20MM) UDI-DI code: 03700780644452 Lot Number: R182X Catalog Number: 53430220 (ELEGANCE 2 LEVEL CERVICAL PLATE 20MM) UDI-DI code: 03700780644452 Lot Numbers: R587X RAA0X Catalog Number: 53430224 (ELEGANCE 2 LEVEL CERVICAL PLATE 24MM) UDI-DI code: 03700780644490 Lot Number: R588X Catalog Number: 53430228 (ELEGANCE 2 LEVEL CERVICAL PLATE 28MM) UDI-DI code: 03700780644513 Lot Numbers: R589X RA80X Catalog Number: 53430230 (ELEGANCE 2 LEVEL CERVICAL PLATE 30MM) UDI-DI code: 03700780644520 Lot Numbers: R556X RA99X Catalog Number: 53430232 (ELEGANCE 2 LEVEL CERVICAL PLATE 32MM) UDI-DI code: 03700780644537 Lot Numbers: R590X RAB3X Catalog Number: 53430234 (ELEGANCE 2 LEVEL CERVICAL PLATE 34MM) UDI-DI code: 03700780644544 Lot Numbers: R591X R880X RA98X Catalog Number: 53430236 (ELEGANCE 2 LEVEL CERVICAL PLATE 36MM) UDI-DI code: 03700780644551 Lot Numbers: R592X R881X RA97X RAU3X Catalog Number: 53430240 (ELEGANCE 2 LEVEL CERVICAL PLATE 40MM) UDI-DI code: 03700780644575 Lot Numbers: R593X RA96X Catalog Number: 53430338 (ELEGANCE 3 LEVEL CERVICAL PLATE 38MM) UDI-DI code: 03700780644582 Lot Numbers: R5B7X RAV7X Catalog Number: 53430344 (ELEGANCE 3 LEVEL CERVICAL PLATE 44MM) UDI-DI code: 03700780644605 Lot Numbers: R5B2X RAY6X Catalog Number: 53430347 (ELEGANCE 3 LEVEL CERVICAL PLATE 47MM) UDI-DI code: 03700780644612 Lot Numbers: R5B3X R8H4X RA95X Catalog Number: 53430350 (ELEGANCE 3 LEVEL CERVICAL PLATE 50MM) UDI-DI code: 03700780644629 Lot Numbers: R579X RA94X Catalog Number: 53430353 (ELEGANCE 3 LEVEL CERVICAL PLATE 53MM) UDI-DI code: 03700780644636 Lot Number: R5B0X Catalog Number: 53430356 (ELEGANCE 3 LEVEL CERVICAL PLATE 56MM) UDI-DI code: 03700780644643 Lot Numbers: R5B1X R5B6X RB63X Catalog Number: 53430362 (ELEGANCE 3 LEVEL CERVICAL PLATE 62MM) UDI-DI code: 03700780644667 Lot Number: R594X

Recalling firm:

Clariance-SAS

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

Recall #:

98481

Lot/product code:

REF/UDI-DI/Lot: 4825/00843997006989/21G6S, 22JHV, 23H03, 23J05, 24DBV, 24NGG, 25ADG, E21D31, E21JWM, E23FVD; 4826/10843997006993/21HVX, 22ELB, 23G31, 23H04, 23HWL, 23J06, 24DBW, 24MNP, 24NGF, 25ADF, E21D32, E21F04, E21JFA, E21KHK

Recalling firm:

Masimo Corporation

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

Recall #:

98481

Lot/product code:

REF/UDI-DI/Lot: 4842/10843997011003/25AJH, 25KMA, 25MSC 4695/10843997016015/24N17, 25BBJ, 25DMH, 25FBR, 24KLV, 24N17, 25AGZ, 25BBJ, 25D10, 25DMH, 25FBR, 25GJM, 25KBF

Recalling firm:

Masimo Corporation

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

Recall #:

D-0401-2026

Lot/product code:

Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027

Recalling firm:

Radnostix

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

Recall #:

98402

Lot/product code:

Lot Code: GTIN: 05050474731776 SKU: DIB00U0210-12 Serial Numbers: 2409342403 2410072403 2409612403 2409692403 2409752403 2891682403 2891132403 2892032403 2531882403 2531902403 2531212403 2530842403 2531242403 2531892403 2531622403

Recalling firm:

AMO Puerto Rico Manufacturing, Inc.

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

Recall #:

98482

Lot/product code:

UDI(s): 10081317028182 10081317028205 10081317028212 10081317028229 10081317028236 10081317028281

Recalling firm:

Mentor Texas, LP.

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

Recall #:

98426

Lot/product code:

UDI-DI (GTIN) 07613327169348 Serial Numbers F61948 F61875 F61710 F62449 F62450 F62451 F62452 F62047 F62048 F62498 F62499 F62500 F61619 F61620 F61621 F61622 F61623 F61624 F61625 F61626 F61627 F61628 F61629 F61630 F61631 F61632 F61633 F61634 F61635 F61636 F61637 F61638 F61639 F61640 F61641 F61642 F61643 F61644 F61645 F61646 F61647 F61648 F61649 F61650 F61651 F61652 F61653 F61654 F61655 F61656 F61657 F61658 F61659 F61660 F61661 F61662 F61663 F61664 F61665 F61666 F61667 F61668 F61669 F61670 F61671 F61672 F61673 F61674 F61675 F61676 F61677 F61678 F61679 F61680 F61681 F61682 F61683 F61684 F61685 F61686 F61687 F61688 F61889 F61890 F61891 F61892 F61893 F61698 F61699 F62448 F61972 F61988 F61989 F62181 F62501 F62502 F62532 F62533 F62432 F62446 F62447 F61595 F61992 F61993 F62125 F62389 F61894 F62123 F61742 F61743 F62117 F62118 F62119 F62433 F62434 F62435 F62436 F62437 F61917 F61918 F61919 F61920 F61921 F61922 F61923 F61924 F61925 F61926 F61927 F61928 F61929 F61930 F61865 F61866 F62159 F62160 F62161 F62325 F62158 F62204 F62205 F62524 F62525 F61695 F61696 F61729 F62083 F62084 F62085 F62086 F62087 F61763 F61764 F61765 F61766 F61767 F61768 F61769 F61770 F61771 F61772 F62431 F62394 F62395 F62396 F62397 F62398 F62399 F62400 F62401 F62402 F62403 F62419 F62420 F62421 F62422 F62423 F62424 F62425 F61998 F61693 F61694 F62530 F62531 F61697 F61700 F62371 F62372 F62373 F62374 F62375 F62195 F62015 F62248 F62249 F62380 F61945 F61946 F61947 F62146 F62147 F62331 F62332 F62333 F62334 F61933 F61934 F61935 F61936 F61937 F61938 F61939 F61940 F61941 F61942 F61943 F61944 F61575 F61576 F61577 F61604 F61605 F61606 F61607 F61608 F61609 F61611 F61612 F61613 F61614 F62010 F62011 F62012 F62013 F62014 F61910 F61911 F61912 F61785 F62044 F62045 F61991 F62462 F61826 F61827 F61828 F61829 F61830 F61831 F61832 F61833 F61834 F61835 F61836 F61837 F62116 F62246 F62247 F62459 F62460 F62518 F62519 F61741 F61745 F61746 F62177 F62178 F62179 F62180 F62453 F62454 F61915 F61916 F62552 F62553 F62554 F62555 F62556 F62557 F62558 F62559 F62126 F62335 F62336 F62337 F62338 F62339 F62340 F62341 F62342 F62343 F62344 F62345 F62346 F62347 F62348 F62349 F62350 F62351 F62352 F62353 F62354 F62355 F61570 F61970 F62503 F62504 F62505 F62506 F62507 F62508 F62509 F62510 F62511 F62512 F62513 F62514 F62515 F62516 F62517 F62305 F62429 F62430 F62303 F62304 F62370 F61788 F61789 F61790 F61791 F61792 F61793 F61794 F61795 F61796 F61797 F62226 F62227 F61881 F61882 F61883 F61884 F61885 F61886 F61887 F61888 F62077 F61711 F61712 F61713 F61714 F62382 F62388 F61717 F61718 F61719 F61720 F61721 F61736 F61737 F61738 F61739 F61740 F62033 F61701 F61702 F61703 F61704 F61705 F61857 F61858 F61786 F61787 F62306 F62307 F62356 F62357 F62358 F62359 F62360 F62361 F61581 F61715 F61716 F62148 F62149 F62150 F62151 F62152 F62153 F61838 F61839 F61840 F61841 F61842 F61843 F61913 F61914 F62108 F62109 F62110 F62111 F62112 F62113 F62127 F62128 F62129 F62130 F62131 F62132 F62120 F62464 F62466 F62467 F62468 F62469 F62470 F62471 F62472 F62473 F62474 F61449 F61450 F62463 F62287 F62288 F62289 F62290 F62291 F62309 F62310 F62311 F62312 F62313 F62314 F62315 F62316 F62317 F62318 F62319 F62320 F62321 F62322 F62323 F62324 F62362 F62363 F62043 F62404 F62405 F62194 F62364 F62365 F62366 F62367 F61735 F61761 F61762 F61747 F61748 F61749 F61760 F62156 F62157 F61864 F61447 F61971 F62016 F62228 F62229 F62230 F62231 F62232 F61582 F61583 F61584 F61585 F62080 F62081 F62196 F62197 F62198 F62529 F62520 F62521 F62522 F62523 F61851 F61852 F61853 F61854 F61855 F61856 F61730 F61731 F61732 F61733 F62497 F61579 F61744 F61750 F61751 F61752 F61753 F61754 F61755 F61999 F62000 F62001 F62002 F62003 F62004 F62005 F62006 F62007 F62008 F61773 F61774 F61990 F62042 F62465 F62250 F62251 F62252 F62253 F62254 F62255 F62256 F62257 F62258 F62259 F62260 F62261 F62262 F62263 F62264 F62266 F62267 F62268 F62269 F62270 F62271 F62272 F62273 F62274 F62275 F62276 F62277 F62278 F62279 F62280 F62281 F62282 F62283 F62284 F62285 F62286 F62292 F62293 F62294 F62295 F62296 F62297 F62298 F62376 F62416 F62417 F61571 F61572 F61573 F61574 F62049 F62050 F62051 F62052 F62009 F62368 F62369 F61931 F61932 F62021 F62022 F62023 F61592 F61593 F62409 F61580 F61589 F61590

Recalling firm:

Stryker Medical Division of Stryker Corporation

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

Recall #:

D-0381-2026

Lot/product code:

Lot #: 5GJ0220, 5GJ0221, 5GJ0222, Exp 04/30/2027

Recalling firm:

Cipla USA, Inc.

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

Recall #:

H-0603-2026

Lot/product code:

Expiration date: 02/24/2026

Recalling firm:

NRS Enterprises, Inc. dba Sunflour Bakery

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

Recall #:

D-0382-2026

Lot/product code:

Lot #: 5GJ0223, Exp 04/30/2027

Recalling firm:

Cipla USA, Inc.

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

Recall #:

D-0387-2026

Lot/product code:

Lot #: 795CP-0005, Exp. Date 06/30/2026

Recalling firm:

HTO Nevada Inc. dba Kirkman

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

Recall #:

D-0386-2026

Lot/product code:

Lot #: 807CP-0003, Exp. Date 07/31/2026.

Recalling firm:

HTO Nevada Inc. dba Kirkman

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

Recall #:

D-0385-2026

Lot/product code:

Lot #: 839CP-0016, Exp. Date 03/31/2026; 839CP-0017, Exp. Date 06/30/2026; 839CP-0018, Exp. Date 08/31/2026; 839CP-0019, Exp. Date 10/31/2026; 839CP-0020, Exp. Date 03/31/2027; 839CP-0021, Exp. Date 07/31/2027; 839CP-0022, Exp.Date 11/30/2027; 839CP-0023, Exp. Date 02/29/2028; 839CP-0024, Exp. Date 07/31/2028.

Recalling firm:

HTO Nevada Inc. dba Kirkman