Recalls affecting Oregon

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

Recall #:

Lot/product code:

Lot # 7240184, 7240185, 7240186, 7240187, Exp Date: 3/31/2026; Lot # 7240278, Exp Date: 5/31/2026.

Recalling firm:

ALEMBIC PHARMACEUTICALS, INC.

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

Recall #:

D-0478-2026

Lot/product code:

Lot: AH250162, Exp 8/31/2027

Recalling firm:

Amneal Pharmaceuticals, LLC

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

Recall #:

D-0405-2026

Lot/product code:

Lot: 4401491, 4401600, 4401603, 4401629, Exp.: 9/31/2026; 4500594, 4500786, 4500920, 4501007, 4501462, Exp.: 3/31/2027.

Recalling firm:

Teva Pharmaceuticals USA, Inc

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

Recall #:

D-0444-2026

Lot/product code:

Lot# 8177156, Exp Date: 02/28/2027

Recalling firm:

Viatris, Inc.

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

Recall #:

D-0479-2026

Lot/product code:

Lot AB6001, exp date 1/15/2027

Recalling firm:

Nephron SC, LLC

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

Recall #:

D-0404-2026

Lot/product code:

Lot: 4401619, Exp.: 09/30/2026; 4501005, 03/31/2027.

Recalling firm:

Teva Pharmaceuticals USA, Inc

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

Recall #:

D-0402-2026

Lot/product code:

Lot #: 1213748, Exp. Date 09/2026; 1215076, 1215077, Exp. Date 10/26.

Recalling firm:

Chiesi USA, Inc.

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

Recall #:

D-0406-2026

Lot/product code:

Lot:4400401, Exp.: 6/30/2026; 4401393, 4401494, 4401604, Exp.: 9/31/2026; 4500564, 4500601, 4500707, 4500796, 4500859, 4500918, 4500919, 4501006, Exp.: 3/31/2027.

Recalling firm:

Teva Pharmaceuticals USA, Inc

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

Recall #:

98565

Lot/product code:

Catalog Number/Art.: 010.5438; UDI-DI: 07630031773937; Order number (lot): 71315US_00729_01_b00, 91076US_03269_00_b00, 72509US_01048_00_b00, 72839US_00065_00_b00, 39133US_11508_02_b00, 4202CA_00558_00_b00, 72630CA_00109_00_b00;

Recalling firm:

Straumann USA LLC

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

Recall #:

98565

Lot/product code:

Catalog Number/Art.: 027.4620; UDI-DI: 07630031713766; Order number (lot): 92465US_12039_00_b00 , 92465US_12040_00_b00 , 92465US_12047_00_b00 , 92465US_12048_00_b00 , 70959US_02227_00_b00 , 94021US_02348_00_b00, 70416US_07543_00_b00 , 91395US_01687_00_b00 , 91545US_03284_00_b00 , 91545US_03285_00_b00 , 71711US_00420_00_b00 , 91853US_06313_00_b00 , 72747US_00247_00_b00;

Recalling firm:

Straumann USA LLC

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

Recall #:

98692

Lot/product code:

Medline Kit SKU DT17360: UDI/DI each 10653160264965, UDI/DI case 00653160264968, Lot Number: 2025101090; Medline Kit SKU IVS1975A: UDI/DI each 10653160327936, UDI/DI case 00653160327939, Lot Number: 2025100890; Medline Kit SKU DT5565B: UDI/DI each 00653160126938, UDI/DI case 10653160126935, Lot Number: 2025103190; Medline Kit SKU EBSI1172B: UDI/DI each 10193489195453, UDI/DI case 20193489195450, Lot Number: 2025110590; Medline Kit SKU DT17360: UDI/DI each 10653160264965, UDI/DI case 00653160264968, Lot Number: 2025110790; Medline Kit SKU EBSI1171A: UDI/DI each 10888277781276, UDI/DI case 40888277781277, Lot Number: 2025111990; Medline Kit SKU EBSI1173A: UDI/DI each 10888277781320, UDI/DI case 40888277781321, Lot Number: 2025112490; Medline Kit SKU DM810: UDI/DI each 10653160304739, UDI/DI case 00653160304732, Lot Number: 2025120990; Medline Kit SKU DM100: UDI/DI each 10653160280101, UDI/DI case 00653160280104, Lot Number: 2026010690; Medline Kit SKU DT5565B: UDI/DI each 00653160126938, UDI/DI case 10653160126935, Lot Number: 2026011390; Medline Kit SKU EBSI1172B: UDI/DI each 10193489195453, UDI/DI case 20193489195450, Lot Number: 2026011390; Medline Kit SKU DT7340: UDI/DI each 00653160091427, UDI/DI case 50653160091422, Lot Number: 2026021090; Medline Kit SKU DM660: UDI/DI each 10653160290667, UDI/DI case 00653160290660, Lot Number: 2026020690; Medline Kit SKU DM810: UDI/DI each 10653160304739, UDI/DI case 00653160304732, Lot Number: 2026020990; Medline Kit SKU EBSI1171A: UDI/DI each 10888277781276, UDI/DI case 40888277781277, Lot Number: 2026021290; Medline Kit SKU EBSI1173A: UDI/DI each 10888277781320, UDI/DI case 40888277781321, Lot Number: 2026021790; Medline Kit SKU EBSI1365A: UDI/DI each 10653160355724, UDI/DI case 00653160355727, Lot Number: 2025121990; Medline Kit SKU EBSI1365A: UDI/DI each 10653160355724, UDI/DI case 00653160355727, Lot Number: 2026020990.

Recalling firm:

Medline Industries, LP

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

Recall #:

98692

Lot/product code:

Medline Kit SKU IV8310E: UDI/DI each 10653160293798, UDI/DI case 00653160293791, Lot Number: 2025102390; Medline Kit SKU IVS1700: UDI/DI each 10653160259213, UDI/DI case 00653160259216, Lot Number: 2025102390; Medline Kit SKU IV8675: UDI/DI each 10653160319160, UDI/DI case 00653160319163, Lot Number: 2025110790; Medline Kit SKU IVSSTK12: UDI/DI each 10653160322511, UDI/DI case 00653160322514, Lot Number: 2025111890; Medline Kit SKU IV6940: UDI/DI each 00653160194210, UDI/DI case 10653160194217, Lot Number: 2025112690; Medline Kit SKU IV8775: UDI/DI each 10888277732537, UDI/DI case 20888277732534, Lot Number: 2025120190; Medline Kit SKU IVSSTK12: UDI/DI each 10653160322511, UDI/DI case 00653160322514, Lot Number: 2025122690; Medline Kit SKU IVS1700: UDI/DI each 10653160259213, UDI/DI case 00653160259216, Lot Number: 2026010590; Medline Kit SKU IV8675: UDI/DI each 10653160319160, UDI/DI case 00653160319163, Lot Number: 2026010990; Medline Kit SKU IV8310E: UDI/DI each 10653160293798, UDI/DI case 00653160293791, Lot Number: 2026011990; Medline Kit SKU IV6940: UDI/DI each 00653160194210, UDI/DI case 10653160194217, Lot Number: 2026012990.

Recalling firm:

Medline Industries, LP

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

Recall #:

98692

Lot/product code:

UDI/DI each 10653160280644, UDI/DI case 00653160280647. Lot Numbers: 2025102090, 2026010990.

Recalling firm:

Medline Industries, LP

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

Recall #:

98574

Lot/product code:

UDI-DI: 0860012888801; Lot 8264701

Recalling firm:

SurgiSmoke Solutions

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

Recall #:

98692

Lot/product code:

UDI/DI each 10653160316459, UDI/DI case 00653160316452, Lot Numbers: 2025100890, 2026011290.

Recalling firm:

Medline Industries, LP

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

Recall #:

98692

Lot/product code:

Medline Kit SKU UROT1044: UDI/DI each 10889942873890, UDI/DI case 40889942873891, Lot Number: 26BBC230; Medline Kit SKU IV8770: UDI/DI each 10653160382638, UDI/DI case 00653160382631, Lot Number: 2025101090; Medline Kit SKU DYNDV2520: UDI/DI each 10653160384045, UDI/DI case 00653160384048, Lot Number: 2025112090; Medline Kit SKU ART255: UDI/DI each 10653160367598, UDI/DI case 00653160367591, Lot Number: 2025111890; Medline Kit SKU DYNDC2969: UDI/DI each 10653160376071, UDI/DI case 00653160376074, Lot Number: 2025120190; Medline Kit SKU DYNDV2520: UDI/DI each 10653160384045, UDI/DI case 00653160384048, Lot Number: 2026010290; Medline Kit SKU IV8770: UDI/DI each 10653160382638, UDI/DI case 00653160382631, Lot Number: 2026010790; Medline Kit SKU ART255: UDI/DI each 10653160367598, UDI/DI case 00653160367591, Lot Number: 2026012090; Medline Kit SKU DYNDC2969: UDI/DI each 10653160376071, UDI/DI case 00653160376074, Lot Number: 2026012390; Medline Kit SKU EBSI1364A: UDI/DI each 10653160363163, UDI/DI case 00653160363166, Lot Number: 2026010690.

Recalling firm:

Medline Industries, LP

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

Recall #:

D-0449-2026

Lot/product code:

Lot, expiry: Lot 4PB0526, 4PB0527, 4PB0528, exp September-2026; Lot 5PB0173, exp January-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-0451-2026

Lot/product code:

Lot, expiry: 4PB0224, exp March-2026; 4PB0505, 4PB0506, 4PB0507, exp September-2026; 5PB0564, exp April-2027

Recalling firm:

Cipla USA, Inc.

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

Recall #:

98591

Lot/product code:

UDI-DI 15099590225872 Lots 538729, 538815, 538898, 539107, 539243

Recalling firm:

Beckman Coulter, Inc.

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

Recall #:

98692

Lot/product code:

Medline Kit SKU DYNDH1520: UDI/DI each 10193489197679, UDI/DI case 20193489197676, Lot Number : 2025101301; Medline Kit SKU DYNDH1520: UDI/DI each 10193489197679, UDI/DI case 20193489197676, Lot Number : 2025113001; Medline Kit SKU EBSI1317: UDI/DI each 10193489195804, UDI/DI case 20193489195801, Lot Number : 2025120390; Medline Kit SKU EBSI1317: UDI/DI each 10193489195804, UDI/DI case 20193489195801, Lot Number : 2026022390.

Recalling firm:

Medline Industries, LP

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

Recall #:

98692

Lot/product code:

UDI/DI each 00653160095890, UDI/DI case 10653160095897, Lot Number: 2025102290

Recalling firm:

Medline Industries, LP

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

Recall #:

D-0450-2026

Lot/product code:

Lot, expiry: 4PB0215, 4PB0216, exp March-2026; 4PB0515, 4PB0516, exp September-2026; 4PB0517, exp September-2026; 5PB0167, exp January-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-0418-2026

Lot/product code:

Lot #1024852; Exp 9/30/2026

Recalling firm:

Amerisource Health Services LLC

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

Recall #:

98574

Lot/product code:

UDI-DI: 408882777851966; Lot 8264501

Recalling firm:

SurgiSmoke Solutions

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

Recall #:

98574

Lot/product code:

UDI-DI: 0860012888818; Lot 8264601

Recalling firm:

SurgiSmoke Solutions