Recalls affecting Virginia

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

Recall #:

H-1096-2026

Lot/product code:

Product Number SMBARML20001 Batch/Lot 025225 and Use By 02/28/2027 Batch/Lot 025255 and Use By 03/31/2027 Batch/Lot 025272 and Use By 03/31/2027 Batch/Lot 025342 and Use By 06/30/2027 Batch/Lot 025364 and Use By 06/30/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

98507

Lot/product code:

UDI-DI: G180DIOWAVESTEALTHMAX0. All software versions prior to, but not including V1.81

Recalling firm:

Technological Medical Advancements LLC

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

Recall #:

98353

Lot/product code:

Lot Code: Version or Model: A-5850.16/1 Device Description: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Lot: 25467933

Recalling firm:

Medartis AG

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

Recall #:

H-1102-2026

Lot/product code:

Product Number SMBARPD20001 Batch/Lot 025233 and Use By 08/31/2026 Batch/Lot 025237 and Use By 08/31/2026 Batch/Lot 025238 and Use By 08/31/2026 Batch/Lot 025239 and Use By 08/31/2026 Batch/Lot 025240 and Use By 08/31/2026 Batch/Lot 025241 and Use By 08/31/2026 Batch/Lot 025261 and Use By 09/30/2026 Batch/Lot 025265 and Use By 09/30/2026 Batch/Lot 025267 and Use By 09/30/2026 Batch/Lot 025268 and Use By 09/30/2026 Batch/Lot 025290 and Use By 10/31/2026 Batch/Lot 025294 and Use By 10/31/2026 Batch/Lot 025329 and Use By 11/30/2026 Batch/Lot 025330 and Use By 11/30/2026 Batch/Lot 025339 and Use By 12/31/2026 Batch/Lot 025343 and Use By 12/31/2026

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1105-2026

Lot/product code:

Product Number SMBARCO20001 Batch/Lot 025226 and Use By 02/28/2027 Batch/Lot 025274 and Use By 04/30/2027 Batch/Lot 025344 and Use By 06/30/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1097-2026

Lot/product code:

Product Number SMBARMB20001 Batch/Lot 025220 and Use By 08/31/2026 Batch/Lot 025223 and Use By 08/31/2026 Batch/Lot 025247 and Use By 09/30/2026 Batch/Lot 025248 and Use By 09/30/2026 Batch/Lot 025251 and Use By 09/30/2026 Batch/Lot 025253 and Use By 09/30/2026 Batch/Lot 025275 and Use By 10/31/2026 Batch/Lot 025281 and Use By 10/31/2026 Batch/Lot 025288 and Use By 10/31/2026 Batch/Lot 025296 and Use By 10/31/2026 Batch/Lot 025335 and Use By 12/31/2026 Batch/Lot 025337 and Use By 12/31/2026 Batch/Lot 026008 and Use By 01/31/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1106-2026

Lot/product code:

Product Number SMBARBO20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025289 and Use By 04/30/2027 Batch/Lot 025325 and Use By 05/31/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1103-2026

Lot/product code:

1) Pure Dark: Product Number SMBARPC20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025218 and Use By 02/28/2027 Batch/Lot 025219 and Use By 02/28/2027 Batch/Lot 025254 and Use By 03/31/2027 Batch/Lot 025266 and Use By 03/31/2027 Batch/Lot 025269 and Use By 03/31/2027 Batch/Lot 025324 and Use By 05/31/2027 Batch/Lot 025338 and Use By 06/30/2027 Batch/Lot 025350 and Use By 06/30/2027 2) Pure Dark Minis: Product Number SMBARPC30001 Batch/Lot 025273 and Use By 03/31/2027 Batch/Lot 025302 and Use By 04/30/2027 Batch/Lot 025303 and Use By 04/30/2027 Batch/Lot 026009 and Use By 07/31/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

98124

Lot/product code:

Model Number: CH-200; (1) Version: 566-16130-23; UDI-DI: 04540217052226; Serial numbers: MP95A9F6A001, MP95A9F6B001, MP95A9F74001, MP95A9F74002, MP95A9F76001, MP95A9F78001; (2) Version: 566-16130-31; UDI-DI: 04540217057436; Serial numbers: MP95AA783001; (3) Version: 566-16130-33; UDI-DI: 04540217057450; Serial numbers: MP95AA983001, MP95AA983002, MP95AA983003, MP95AA985001, MP95AA985003, MP95AA985002, MP95AA988001, MP95AA988002;

Recalling firm:

FUJIFILM Healthcare Americas Corporation

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

Recall #:

98159

Lot/product code:

Model Number: 701055720; UDI-DI: 04037691816432; Serial Numbers: All units impacted;

Recalling firm:

Maquet Cardiopulmonary Gmbh

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

Recall #:

H-1100-2026

Lot/product code:

Product Number SMBARMC20001 Batch/Lot 025245 and Use By 03/31/2027 Batch/Lot 025283 and Use By 04/30/2027 Batch/Lot 025322 and Use By 05/31/2027 Batch/Lot 025328 and Use By 05/31/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1104-2026

Lot/product code:

Product Number SMBARSS20001 Batch/Lot 026013 and Use By 07/31/2027 Batch/Lot 026014 and Use By 07/31/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

98353

Lot/product code:

Lot Code: Version or Model: A-5750.16/1 Device Description: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Lot: 25472432

Recalling firm:

Medartis AG

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

Recall #:

H-1099-2026

Lot/product code:

Product Number SMBARLR20001 Batch/Lot 025204 and Use By 01/31/2027 Batch/Lot 025205 and Use By 01/31/2027 Batch/Lot 025212 and Use By 02/28/2027 Batch/Lot 025216 and Use By 02/28/2027 Batch/Lot 025259 and Use By 03/31/2027 Batch/Lot 025260 and Use By 03/31/2027 Batch/Lot 026037 and Use By 08/31/2027 Batch/Lot 026040 and Use By 08/31/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1101-2026

Lot/product code:

Product Number SMBARMF20001 Batch/Lot 025230 and Use By 02/28/2027 Batch/Lot 025287 and Use By 04/30/2027 Batch/Lot 025345 and Use By 06/30/2027

Recalling firm:

Spring & Mulberry Inc.

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

Recall #:

H-1178-2026

Lot/product code:

Product distributed between April of 2022 until December 8th of 2025.

Recalling firm:

Modern Warrior Life, LLC

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

Recall #:

98333

Lot/product code:

IR PACK UDI-DI (ea) 10195327621780 UDI-DI (case) 40195327621781 Kit lots 24BBP627 24DBO029 24FBI148 24JBA858 24KBD925 24LBG978 25ABQ002 25EBV162; NO CATHETER DIALYSIS INSERTION UDI-DI (ea) 10195327675219 UDI-DI (case) 40195327675210 Kit Lots 24EBM915 24GBC287

Recalling firm:

Medline Industries, LP

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

Recall #:

98333

Lot/product code:

Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 UDI-DI (ea) 10193489111538 UDI-DI (case) 20193489111535 Kit lots 2024052090 2024072690 2024100390 2024121290 2025020490 2025041590 2025062790 2025090890 Medline DIALYSIS DRESSING CHANGE KIT SKU EBSI1107 UDI-DI (ea) 10889942723508 UDI-DI (case) 40889942723509 Kit lots 2024051690 2024073190 2024092490 2024121190 2025020790 2025032790 2025052990 EBSI1596 UDI-DI (ea) 10653160357162 UDI-DI (case) 00653160357165 Kit lots 2024070190 2024082390 2024102390 2024121790 2025031090 2025040190 2025052790 2025072890 EBSI1781 UDI-DI (ea) 10653160379638 UDI-DI (case) 00653160379631 Kit lots 2024100490 2024123090 EBSI1812 UDI-DI (ea) 10653160386735 UDI-DI (case) 00653160386738 Kit lots 2025032190 2025052990 Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT SKU DT22630 UDI-DI (ea) 10653160345343 UDI-DI (case) 00653160345346 Kit lots 2024050680 2024072980 2024090380 2024111290 2024121190 2025032890 2025061790 2025072390 Medline DIALYSIS/PHERESIS DRESSING CHANGE KIT SKU EBSI1470 UDI-DI (ea) 10193489199307 UDI-DI (case) 20193489199304 Kit lots 2024052080 2024070880 2024110490 2025010290 2025022090 2025030390 2025040990 2025072990 Centurion VASCATH DRESSING CHANGE TRAY SKU DT22845 UDI-DI (ea) 10653160355151 UDI-DI (case) 00653160355154 Kit lots 2024060790 2024080790 2024100990 2024112590 2025042490 2025082090

Recalling firm:

Medline Industries, LP

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

Recall #:

98333

Lot/product code:

UDI-DI (ea) 10653160373582 UDI-DI (case) 00653160373585 Kit lots 2024051380 2024052080 2024052180 2024052280 2024071580 2025061790 2025072990

Recalling firm:

Medline Industries, LP

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

Recall #:

98333

Lot/product code:

Medline ADD A CATH DIALYSIS KIT SKU ECVC8415A UDI-DI (ea) 10653160383628 UDI-DI (case) 00653160383621 Kit lots 2024121390 2025033190 Centurion CENTRAL LINE INSERTION TRAY SKU DT19810 UDI-DI (ea) 10653160368755 UDI-DI (case) 00653160368758 Kit lot 2025041090 Centurion DIALYSIS BUNDLE WITH NO CATHETTER SKU CVI4310A UDI-DI (ea) 10653160374978 UDI-DI (case) 00653160374971 Kit lots 2024051490 2025021290 2025051390 2025091090 Medline DIALYSIS CAP CHANGE KIT SKU DYNDC2425 UDI-DI (ea) 10653160375845 UDI-DI (case) 00653160375848 Kit lots 2024060690 2024101690 2024103190 2025010890 2025040190 Medline DIALYSIS CHANGE KIT SKU EBSI1453A UDI-DI (ea) 10653160383475 UDI-DI (case) 00653160383478 Kit lots 2024050790 2024051390 2024082290 2024111990 2025013090 2025032090 2025050190 2025062790 Centurion HEMODIALYSIS ACCESS KIT SKU DT12970 UDI-DI (ea) 10653160368922 UDI-DI (case) 00653160368925 Kit lots 2025040401 2025081401 Medline LARGE BORE, DIALYSIS, ENHANCED SECUREMENT SKU EBSI1741 UDI-DI (ea) 10653160374527 UDI-DI (case) 00653160374520 Kit lots 2024061780 2024070180 2024081280 2024111290 2025012490 2025032690 2025051390 2025061790 2025071490 2025072190

Recalling firm:

Medline Industries, LP

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

Recall #:

98333

Lot/product code:

SKU DYNDA2705 UDI-DI (ea) 10193489468632 UDI-DI (case) 40193489468633 Kit lots 24DBL787 24HBR630 25ABH699 25DBV209 25GBQ405 SKU DYNJ63347A UDI-DI (ea) 10193489278064 UDI-DI (case) 40193489278065 Kit lots 24AMC874 24AME139 24AMH820 24BMF097 24CMF691 24GMB769 24GMK036 24IMC124 24LMA110 25AMJ634 25GMD386 25IMB510 25JMI708

Recalling firm:

Medline Industries, LP

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

Recall #:

98333

Lot/product code:

UDI-DI (ea) 10195327015954 UDI-DI (case) 40195327015955 Kit lots 24IME953 25CMA708

Recalling firm:

Medline Industries, LP

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

Recall #:

98360

Lot/product code:

Model/Catalog Number: SPL-SR, contains generator SPL-G; UDI: SPL-SR 00821925043824, SPL-G 00821925044203; Serial Numbers: CG5026, CG5027, CG5028, CG5029, CG5030, CG5031, CG5032, CG5033, CG5034, CG5035, CG5036, CG5037, CG5039, CG5040, CG5041, CG5042, CG5043, CG5045, CG5046, CG5047, CG5048, CG5049, CG5050, CG5051, CG5052, CG5053, CG5054, CG5055, CG5056, CG5057, CG5058, CG5059, CG5060, CG5061, CG5062, CG5063, CG5065, CG5066, CG5067, CG6037, CG6061, CG6069, CG6070, CG6071, CG6088, CG6094, CG6095, CG6096, CG6097, CG6098, CG6099, CG7000, CG7001, CG7002, CG7003;

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98329

Lot/product code:

1) DYKMBNDL130, UDI-DI: 10193489479027(each), 40193489479028(case), Lot Number: 21BBB580; 2) DYKMBNDL130, UDI-DI: 10193489479027(each), 40193489479028(case), Lot Number: 21ABJ543; 3) DYKMBNDL130, UDI-DI: 10193489479027(each), 40193489479028(case), Lot Number: 21ABC197; 4) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22GLB021; 5) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22GLA694; 6) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22FLA745; 7) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22ELA008; 8) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22DLA407; 9) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22CLA448; 10) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22BLA721; 11) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 22ALA593; 12) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21JLA910; 13) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21ILA163; 14) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21HLA740; 15) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21GLA677; 16) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21FLA214; 17) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21ELA080; 18) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21DLA326; 19) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21CLA621; 20) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21CLA391Z; 21) DYKMBNDL130A, UDI-DI: 10193489829594(each), 40193489829595(case), Lot Number: 21CLA391; 22) DYKMBNDL4, UDI-DI: 10193489477627(each), 40193489477628(case), Lot Number: 21DLA343; 23) DYKMBNDL4, UDI-DI: 10193489477627(each), 40193489477628(case), Lot Number: 21ALA631; 24) DYKMBNDL4, UDI-DI: 10193489477627(each), 40193489477628(case), Lot Number: 21ALA056; 25) LC295, UDI-DI: 10653160322702(each), 00653160322705(case), Lot Number: 2025110490; 26) DYKM1977C, UDI-DI: 10653160381105(each), 00653160381108(case), Lot Number: 2024110190; 27) CVI4300, UDI-DI: 10653160294313(each), 00653160294316(case), Lot Number: 2020120950

Recalling firm:

Medline Industries, LP

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

Recall #:

98252

Lot/product code:

Model/Catalog Number: KD-411Q-0730; Material REFs: (1) 5858230, (2) N6221731, (3) N6221740; UDI-DI: (1)04953170466557, (2)04953170466557, (3)04953170466557; All Lots with a valid expiration date

Recalling firm:

Olympus Corporation of the Americas