Recalls affecting New Mexico

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

Recall #:

D-0219-2026

Lot/product code:

Lot # F2400244, Exp Date: 10/31/2026

Recalling firm:

Dr. Reddy's Laboratories, Inc.

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

Recall #:

98060

Lot/product code:

Kit Code: LLOF1000-17; UDI : 10809160460726, Lot No : 1651709

Recalling firm:

AVID Medical, Inc.

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

Recall #:

98288

Lot/product code:

Model No. A22041T; UDI: 04042761020978; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A22040T; UDI: 04042761029360; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A22043T; UDI: 04042761021012; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. WA22017T; UDI: 04042761051521; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A37004A; UDI: 04042761023092; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A2641; UDI: 04042761004060; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A42011A; UDI: 04042761023658; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model: A22014A (UDI: 04042761020893) and A22014T (UDI: 04042761020909). All lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A2666; UDI: 04042761004244; All Lots

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A22040A; UDI: 04042761029339; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. Model No. A22041A; UDI: 04042761020961; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. WA22017A; UDI: 04042761051514; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

98288

Lot/product code:

Model No. A2660T; UDI: 04042761004183; All Lots.

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

97923

Lot/product code:

Model/Catalog Number: MP01860; UDI Number: 04048675420699; Lot numbers: All lot numbers;

Recalling firm:

Draeger, Inc.

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

Recall #:

97923

Lot/product code:

Model/Catalog Number: MP01855; UDI Number: 04048675420705; Lot numbers: All lot numbers;

Recalling firm:

Draeger, Inc.

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

Recall #:

97923

Lot/product code:

Model/Catalog Number: MP01840; UDI Number:04048675420736; Lot numbers: All lot numbers

Recalling firm:

Draeger, Inc.

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

Recall #:

97923

Lot/product code:

Model/Catalog Number: MP01845; UDI Number: 04048675420729; Lot numbers: All lot numbers;

Recalling firm:

Draeger, Inc.

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

Recall #:

97992

Lot/product code:

Catalog Numbers: COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 UDI-DI code: 15099590233686 Lot Numbers: 2510410 2510420 2510450 3557500 3557510 3557540 3557560 3557570 3557640 3557650 3557660 3557670 3557680 3557700 3557710 3557850 3557920 3557930 3558000 3558030 3558040 3558060 3558090 3558100 3558110 3558120 3558140 3558150 3558160 3558170

Recalling firm:

Beckman Coulter, Inc.

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

Recall #:

H-0249-2026

Lot/product code:

All batches and codes within expiry Finished Product Quantity 08NOV2023 to 08NOV2025 UPC Codes: Single Can: 8 50044 96800 8; Sams Club 2PK: 00850044968893; Amazon 2PK: 00850044968053; Anywhere pack: 8 50044 96802 2; 1-Count Sample Unit Anywhere Pack: 850044968015

Recalling firm:

ByHeart, INC.

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

Recall #:

D-0198-2026

Lot/product code:

Lot #100068692, Exp.: 04/30/2027

Recalling firm:

Teva Pharmaceuticals USA, Inc

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

Recall #:

97932

Lot/product code:

UDI-DI: 15099590180249; Lot Numbers: P243943, P243971, P244202 P244344, P244345, P250001, P250002, P250003, P250004 and P250005

Recalling firm:

Beckman Coulter, Inc.

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

Recall #:

97994

Lot/product code:

Model/Catalog Number: R54544-18-SG; UDI-DI: 050552709TF06DXY; Lot Code: 496809, 501616, 497346, 501710, 497665, 502431, 498972, 503735, 499909, 503937, 500782, 504573, 501256, 504824;

Recalling firm:

Rocket Medical Plc

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

Recall #:

97994

Lot/product code:

Model/Catalog Number: R54544-12-SG; UDI-DI: 050552709TF06DXY; Lot Code: 497012, 502660, 497561, 502780, 497763, 502978, 498069, 503202, 499335, 503384, 499541, 503406, 499903, 503536, 500405, 503733, 500630, 503900, 500706, 504179, 500812, 504397, 501030, 504628, 501615, 504822;

Recalling firm:

Rocket Medical Plc