Recalls affecting Delaware

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

Recall #:

97801

Lot/product code:

Name/Lot(Expiration): Vivoo Vaginal pH Test/2024032219(03/21/2026)

Recalling firm:

Changchun Wancheng Bio-Electron Co., Ltd.

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

Recall #:

97801

Lot/product code:

Name/Lot(Expiration): Vivoo Sodium Test/2024013123(01/30/2026); Vivoo Vitamin C Test/2024013124(01/30/2026); Vivoo Hydration Test/2024013119(01/30/2026), 2025051519(05/14/2027)

Recalling firm:

Changchun Wancheng Bio-Electron Co., Ltd.

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

Recall #:

97801

Lot/product code:

Name/Lot(Expiration): LotFancy Urinary Tract Infection Urine (UTI) Test Strips/2025062001(06/19/2027); LotFancy URS-3N Test Strip/2025033101(03-30-2027), 2025080801(08-07-2027), 2025090844(09-07-2027); PALINOIA UTI-10 PARAMETER REAGENT STRIPS/2025042110(04-20-2027), 2025021001(02-20-2027); Vaunn Medical 8-in-1 Urinalysis Reagent Strip/2024032508(03/24/2026), 2024071602(07/15/2026), 2024102108(10/20/2026); JNW Direct 4-in-1 UTl Urinalysis Test Strips/30D25WC(04/29/2027), 02D25WC(04/01/2027), 30E25WC(05/29/2027), 10H24WC(07/10/2026); Urinify STRENGTH/202403103-6(01/03/2026), 202504103-6(01/01/2027), 202505103-6(06/01/2027), 202504103-3(01/01/2027), 202505103-3(06/01/2027); Urinify ESSENTIAL/202403104-6(01/03/2026), 202504104-6(01/01/2027), 202505104-6(06/01/2027), 202504104-3(01/01/2027), 202505104-3(06/01/2027); Urinify Urinary Tract Infection (UTI)/202501105-5(01/02/2027)

Recalling firm:

Changchun Wancheng Bio-Electron Co., Ltd.

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

Recall #:

97801

Lot/product code:

Name/Lot(Expiration): Menopause Test Cassette (Urine)/GT-FSH 20251601(05-2027)

Recalling firm:

Changchun Wancheng Bio-Electron Co., Ltd.

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

Recall #:

97801

Lot/product code:

Name/Lot(Expiration): Male Fertility Sperm Test for Home Use (Cassette)/GT-SPA 20251601(05-2027)

Recalling firm:

Changchun Wancheng Bio-Electron Co., Ltd.

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

Recall #:

97801

Lot/product code:

Name/Lot(Expiration): The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips/2024032508(03/24/2026), 2024071602(07/15/2026), 2024102108(10/20/2026); URIMED Urinalysis Reagent Strips URS-5, Rapid UTI Test Includes Ketones: Leukocytes, Nitrite, pH, Ketone, Protein/2025043007(04/29/2027); Vivoo Ketone Test/2024013122(01/30/2026)

Recalling firm:

Changchun Wancheng Bio-Electron Co., Ltd.

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

Recall #:

98125

Lot/product code:

UDI: 1041CE 00888277446727 (ea) 40888277446725 (case); HUD1035 10197344011575 (ea) 20197344011572 (case); HUD1042 10197344011544 (ea) 20197344011541 (case); HUD1930 10197344009626 (ea) 20197344009623 (case); HUDRHO41U 10197344010646 (ea) 20197344010643 (case) Lots: 24DOA701 25EOA321 25EOA589 25EOA724 25EOA730 25EOA781 25EOA857 25FOA151 25FOA152 25FOA153 25FOA206 25FOA218 25FOA219 25FOA220 25FOA221 25FOA275 25FOA287 25FOA288 25FOA418 25FOA419 25FOA420 25FOA421 25FOA422 25FOA514 25FOA515 25FOA524 25FOA525 25FOA551 25FOA552 25FOA553 25FOA556 25FOA557 25FOA642 25FOA643 25FOA647 25FOA648 25FOA649 25FOA650 25FOA722 25FOA740 25FOA864 25FOA865 25FOA866 25GOA055 25GOA065 25GOA066 25GOA077 25GOA078 25GOA096 25GOA098 25GOA190 25GOA210 25GOA211 25GOA328 25GOA363 25GOA364 25GOA365 25GOA366 25GOA367 25GOA437 25GOA445 25GOA446 25GOA561 25GOA562 25GOA563 25GOA564 25GOA565 25GOA640 25GOA641 25GOA648 25GOA655 25GOA735 25GOA736 25GOA756 25GOA757 25GOA758 25GOA759 25GOA760 25GOA761 25GOA766 25GOA830 25GOA994 25GOA998 25HOA009 25HOA011 25HOA017 25HOA018 25HOA019 25HOA020 25HOA021 25HOA022 25HOA060 25HOA061 25HOA071 25HOA247 25HOA249 25HOA252 25HOA253 25HOA254 25HOA255 25HOA256 25HOA316 25HOA335 25HOA372 25HOA373 25HOA452 25HOA455 25HOA456 25HOA457 25HOA458 25HOA459 25HOA460 25HOA462 25HOA469 25HOA474 25HOA478 25HOA532 25HOA533 25HOA538 25HOA629 25HOA630 25HOA631 25HOA632 25HOA633 25HOA639 25HOA644 25HOA723 25HOA724 25HOA734 25HOA829 25HOA830 25HOA831 25HOA832 25HOA833 25HOA853 25IOA020 25IOA021 25IOA090 25IOA097 25IOA163 25IOA164 25IOA165 25IOA166 25IOA244 25IOA246 25IOA247 25IOA253 25IOA363 25IOA364 25IOA365 25IOA366 25IOA367 25IOA368 25IOA369 25IOA410 25IOA438 25IOA439 25IOA520 25IOA521 25IOA522 25IOA523 25IOA524 25IOA525 25IOA526 25IOA527 25IOA637 25IOA638 25IOA668 25IOA682 25IOA683 25IOA684 25IOA685 25IOA686 25IOA687 25IOA688 25IOA743 25IOA787 25JOA027 25JOA032 25JOA047 25JOA048 25JOA049 25JOA050 25JOA051 25JOA052 25JOA053 25JOA179 25JOA213 25JOA215 25JOA243 25JOA246 25JOA247 25JOA248 25JOA249 25JOA250 25JOA251 25JOA252 25JOA253 25JOA386 25JOA430 25JOA467 25JOA561 25JOA562 25JOA563 25JOA564 25JOA579 25JOA670 25JOA675 25JOA757 25JOA758 25JOA760 25JOA762 25JOA763 25JOA778 25JOA779 25JOA780 25JOA832 25JOA835 25JOA856 25JOA940 25JOA941 25JOA942 25KOA050 25KOA051

Recalling firm:

Medline Industries, LP

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

Recall #:

98106

Lot/product code:

Product Code: LVP-SW-0005; UDI: 00811505030122; Software versions 5.10.2 and prior.

Recalling firm:

Fresenius Kabi USA, LLC

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

Recall #:

H-0373-2026

Lot/product code:

Lot number(s): 1000572981 1000570737 1000570092 1000572487

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

H-0371-2026

Lot/product code:

Lot number(s): 1000570107 1000570766 1000572513

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

D-0199-2026

Lot/product code:

Lot #: (a): Lot 17232401, exp 11/2025; Lot 17240974, exp 05/2026 (b): Lot 17232401, exp 11/2025; Lot 17240974, exp 05/2026 (c): Lot 17232401, exp 11/2025; Lot 17240974, exp 05/2026

Recalling firm:

Glenmark Pharmaceuticals Inc., USA

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

Recall #:

H-0374-2026

Lot/product code:

Lot numbers: 1000570750 1000572499 1000572514

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

H-0368-2026

Lot/product code:

Lot numbers: 1000570725 1000572476 1000570724 1000572475 1000570726 1000570727 1000572477

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

H-0367-2026

Lot/product code:

Lot Numbers: 1000572472 1000570734 1000570735 1000570736 1000572482 1000572483 1000572485

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

H-0370-2026

Lot/product code:

Lot number(s): 1000572486

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

H-0372-2026

Lot/product code:

Lot number(s): 1000570093 1000570738

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

H-0369-2026

Lot/product code:

Lot number(s): 1000572486

Recalling firm:

Ambriola Co., Inc., The

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

Recall #:

98103

Lot/product code:

08496633190 lot 840183 exp. 02/26 08496633190 lot 874011 exp. 10/26 08496609190 lot 840177 exp. 05/26

Recalling firm:

Roche Diagnostics Operations, Inc.

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

Recall #:

98028

Lot/product code:

CP App: UDI-DI 00763000273668 all software versions prior to v.1.0.4489 are affected The implanted devices are not affected.

Recalling firm:

Medtronic Neuromodulation

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

Recall #:

97712

Lot/product code:

Firmware Version: 1.48. REF/UDI-DI: 323/10885403512667, 324/10885403512681, 352/10885403512674, 1149-00/10885403517822, 1152-00/10885403517839, 1155-00/10885403521300, 1116-00/10885403512605

Recalling firm:

CareFusion 303, Inc.

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

Recall #:

D-0221-2026

Lot/product code:

Lot#: C274-000047958; Exp. December 19, 2025

Recalling firm:

Fagron Compounding Services

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

Recall #:

98032

Lot/product code:

UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040

Recalling firm:

Vortex Surgical Inc.

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

Recall #:

97986

Lot/product code:

Lot Code: UDI: 00724995176662, 00724995176679, 00724995176655 Serial numbers of distributed units: 3619725008, 3619725011, 3619725013, 3621625010, 3621625011, 3621625013, 3621625014, 3621625015, 3621925001, 3621925002, 3621925005, 3621925010, 3622425005, 3622725005, 3622725011, 3622725012, 3623125006, 3623425016, 3623825008, 3624025002, 3624025008, 3624525007

Recalling firm:

Steris Corporation

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

Recall #:

97986

Lot/product code:

Lot Code: UDI:00724995176587, 00724995176594, 00724995176570 Serial number of distributed units: 3619625011, 3621625009, 3621625012, 3621925006, 3621925009, 3622425006, 3622725007, 3623425005, 3623825002, 3624525002

Recalling firm:

Steris Corporation

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

Recall #:

98019

Lot/product code:

Part No. 0020007400; UDI: 08426950087649; Lot No. (Exp. Date) N0542231(2026-06-30), N0250088(2027-04-30, N0452249 (2027-06-30).

Recalling firm:

Instrumentation Laboratory