Recalls affecting Virginia

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

Recall #:

99021

Lot/product code:

Kit Code: AMPK48-01. UDI-DI: 10809160472798. Lot Number: 334669. Expiration Date: 8/27/2028.

Recalling firm:

AVID Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007844, Lot Numbers 30371318, 30375469, 30383056

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98918

Lot/product code:

UDI: 06429811532083; All lots until the IFU update has been implemented

Recalling firm:

SURGIFY MEDICAL OY

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007769, Lot Numbers 30371312 and 30373421

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007813, Lot Number 30370718

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007769, Lot Numbers 30371312 and 30373421

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007752, Lot Number 30370713

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

99339

Lot/product code:

UDI-DI 10809160388495 Lots 1561685 1575926 1583048 1584017 1589652 1595715 1599634 1605749 1611810 1621476 1637222 1637224 1637225 1643118 1645143 1645637 1663929 1663930 1663931 1663932

Recalling firm:

AVID Medical, Inc.

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

Recall #:

99021

Lot/product code:

Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028

Recalling firm:

AVID Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007837, Lot Numbers 30371847, 30374834, 30378748, 30380347

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98979

Lot/product code:

Lot #: A6DLA001 Unique Device Identifier: 10711234170373

Recalling firm:

Accriva Diagnostics, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007516, Lot Numbers 30365231, 30371022, 30373824, 30378385, 30383807, 30385321

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98918

Lot/product code:

UDI: 06429811532335 ; All lots until the IFU update has been implemented

Recalling firm:

SURGIFY MEDICAL OY

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

Recall #:

98907

Lot/product code:

UDI-DI: 10350770007790, Lot Numbers 30370715, 30371329, 30375466

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

98907

Lot/product code:

UDI-DI 10350770007523, Lot Numbers 30365232, 30367019, 30380107

Recalling firm:

Avanos Medical, Inc.

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

Recall #:

99021

Lot/product code:

Kit Code: AMTS70-01. UDI-DI: 10809160469972. Lot Number: AMTS70-01. Expiration Date: 9/2/2028.

Recalling firm:

AVID Medical, Inc.

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

Recall #:

D-0544-2026

Lot/product code:

Lots: a) M411146, Expires: 08/2026; M502098, M502097, Expires: 01/2027; b) M411145, Expires: 08/2026.

Recalling firm:

Zydus Pharmaceuticals (USA) Inc

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

Recall #:

H-1118-2026

Lot/product code:

07317100316

Recalling firm:

George J Howe Company, Inc.

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

Recall #:

98891

Lot/product code:

1. Product Number (CFN): 8888221413; UDI-DI: 10884521788541; Lot numbers: 241620022, 252020038; 2. Product Number (CFN): 8888222416; UDI-DI: 10884521788602; Lot numbers: 241690023, 241830147; 3. Product Number (CFN): 8888221416; UDI-DI: 10884521788558; Lot numbers: 251250041, 251740190, 252020039, 252090031, 253350256; 4. Product Number (CFN): 8888222420; UDI-DI: 10884521788619; Lot numbers: 251740186, 252510026, 253280016; 5. Product Number (CFN): 8888221420; UDI-DI: 10884521788565; Lot numbers: 241620407, 251950032; 6. Product Number (CFN): 8888222424; UDI-DI: 10884521788626; Lot number: 243040007; 7. Product Number (CFN): 8888221424; UDI-DI: 10884521788572; Lot numbers: 241200034, 251250039, 252020037; 8. Product Number (CFN): 8888221430; UDI-DI: 10884521788589; Lot number: 251250042; 9. Product Number (CFN): 8888233413; UDI-DI: 10884521788718; Lot number: 250310009; 10. Product Number (CFN): 8888233416; UDI-DI: 10884521788725; Lot numbers: 250350008, 250690152, 250690153, 250870012, 251010012, 251010013, 251320332, 251320333, 251390368, 251390369, 252580023; 11. Product Number (CFN): 8888233420; UDI-DI: 10884521788732; Lot numbers: 250870013, 250970052, 251320330, 251320331; 12. Product Number (CFN): 8888231420; UDI-DI: 10884521788688; Lot numbers: 241690216, 252020046, 252230023, 252580025; 13. Product Number (CFN): 8888233424; UDI-DI: 10884521788749; Lot numbers: 251740197, 252300054; 14. Product Number (CFN): 8888231424; UDI-DI: 10884521788695; Lot numbers: 251460351, 251740196, 252020045, 252230022, 252580024; 15. Product Number (CFN): 8888231430; UDI-DI: 10884521788701; Lot number: 252730009; 16. Product Number (CFN): 8888231413; UDI-DI: 10884521788664; Lot number: 250310010; 17. Product Number (CFN): 8888231416; UDI-DI: 10884521788671; Lot numbers: 252230021, 252510030, 252650294, 253140280; 18. Product Number (CFN): 8888213416; UDI-DI: 10884521788527; Lot number: 252300325; 19. Product Number (CFN): 8888211416; UDI-DI: 10884521788435; Lot numbers: 241060237, 250830187, 250900067, 251250037, 251430012, 252870014; 20. Product Number (CFN): 8888213420; UDI-DI: 10884521788534; Lot number: 252300051; 21. Product Number (CFN): 8888211420; UDI-DI: 10884521788442; Lot numbers: 241480021, 242390056, 250070005, 250310011, 250310012, 250760180, 250900066, 251250035, 251950034; 22. Product Number (CFN): 8888212413; UDI-DI: 10884521788473; Lot number: 242950260; 23. Product Number (CFN): 8888211413; UDI-DI: 10884521788428; Lot number: 252510028; 24. Product Number (CFN): 8888212416; UDI-DI: 10884521788480; Lot numbers: 243160028, 250760159, 251250036, 251320325; 25. Product Number (CFN): 8888212420; UDI-DI: 10884521788497; Lot numbers: 241350005, 250310006, 251740192, 252160037; 26. Product Number (CFN): 8888211424; UDI-DI: 10884521788459; Lot numbers: 250830185, 250830186, 250900298, 250900299, 251740179, 251950033;

Recalling firm:

Mozarc Medical US LLC

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

Recall #:

D-0514-2026

Lot/product code:

Lot#: a) PA10774, Exp. May 2026; b) PA10794, PA12174, Exp. Jun 2026; c) PA10804, Exp. Jun-26.

Recalling firm:

Ajanta Pharma Ltd.

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

Recall #:

H-1119-2026

Lot/product code:

07317100320

Recalling firm:

George J Howe Company, Inc.

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

Recall #:

D-0515-2026

Lot/product code:

Lot#: PA07434, Exp. May 2026.

Recalling firm:

Ajanta Pharma Ltd.