Recalls affecting New Mexico

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

Recall #:

99332

Lot/product code:

REF/UDI-DI/Lots: 56800095/10889981149352/181559, 181550 02-8000-095/10889981149314/181559, 181550

Recalling firm:

IsoTis OrthoBiologics, Inc.

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

Recall #:

D-0734-2026

Lot/product code:

Lot #: 3241653, Exp 4/30/2027

Recalling firm:

MYLAN PHARMACEUTICALS INC

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

Recall #:

99346

Lot/product code:

UDI-DI (01)00887868507793(17)360407(10)67818791; Lot 67818791

Recalling firm:

Biomet, Inc.

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

Recall #:

99344

Lot/product code:

UDI-DI: 05070002420378, Lot Number: KE132603

Recalling firm:

Aniara Diagnostica LLC

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

Recall #:

99346

Lot/product code:

UDI-DI (01)00887868507816(17)360221(10)67818764; Lot 67818764 Model No 475630; UDI-DI (01)00887868507816(17)360401(10)67818768; Lot 67818768 Model No 475630; UDI-DI (01)00887868507816(17)360428(10)67954534; Lot 67954534

Recalling firm:

Biomet, Inc.

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796150. GTIN: 04546540389954. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99346

Lot/product code:

UDI-DI (01)00887868507809(17)360228(10)67818772; Lot 67818772

Recalling firm:

Biomet, Inc.

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796120. GTIN: 04546540389947. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796090. GTIN: 04546540389930. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99344

Lot/product code:

UDI-DI: 05070002420392, Lot Number: KE132601

Recalling firm:

Aniara Diagnostica LLC

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

Recall #:

H-1221-2026

Lot/product code:

No Lot Codes Used Best by dates: March 28, 2027, June 01, 2027, August 15, 2027, August 25, 2027 and October 15, 2027

Recalling firm:

JINA F&C

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796060. GTIN: 04546540389923. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796050. GTIN: 04546540389916. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796040. GTIN: 04546540389909. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99246

Lot/product code:

Catalog Number: 50796030. GTIN: 04546540389893. All lot numbers.

Recalling firm:

Stryker GmbH

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

Recall #:

99346

Lot/product code:

UDI-DI (01)00887868507823(17)360224(10)67818769; Lot 67818769 Model No 475635; UDI-DI (01)00887868507823(17)360225(10)67818770; Lot 67818770

Recalling firm:

Biomet, Inc.

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

Recall #:

D-0772-2026

Lot/product code:

Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.

Recalling firm:

Victory Medical Center Pharmacy

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

Recall #:

99344

Lot/product code:

UDI-DI: 05070002420385, Lot Number: KE132602

Recalling firm:

Aniara Diagnostica LLC

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

Recall #:

99346

Lot/product code:

UDI-DI (01)00887868507830(17)360316(10)67818792; Lot 67818792

Recalling firm:

Biomet, Inc.

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

Recall #:

99361

Lot/product code:

Product Number: 860439. UDI: (01)00884838094826. Serial Numbers: US42510185, US42510184, US52510209, US52510200, US52510226, US52510228, US62510247, US62510250, US62510256, US72510286, US82510299, US82510307, US82510300, US82510313, US82510318, US82510314, US82510335, US82510336, US82510341, US82510325, US92510351, US92510353, US92510354, US92510361, US92510362, US92510370, USN2510413, USN2510414, USN2510434, USN2510435, USN2510437, USD2510506, USD2510519, US12610582, USD2510513, US12610598, US22610609, US22610683, US22610691, US22610689, US32610737, US32610744, US32610759, US32610766, US32610749, US32610739, US32610751, USD2510516, USD2510510, USD2510517, USD2510529, USD2510509, US32610752, US32610753, US32610879, US32610880, US32610901, US32610914, US42610946, US32610915, US32610941, US32610932, US42610943, US42610942, US42610959, US42610958, US42610955, US42610974, US42610967, US42610956, US42610993, US42610960, CN72410032, CN92410061, CNO2410064, CNO2410068, CNN2410075, CND2410080, CND2410101, CND2410103, CN12510116, CN12510136, CN22510140, CN22510142, CN22510146, CN32510148, CN32510161, CN42510168, CN42510181, CN42510183, CN52510204, CN52510201, CN52510217, CN62510239, CN62510241, CN62510242, CN62510253, CN62510254, CN62510251, CN72510275, CN72510282, CN72510281, CN72510285, CN72510289, CN72510288, CN72510293, CN72510297, CN82510305, CN82510310, CN82510323, CN82510324, CN82510321, CN92510343, CN92510364, CN92510365, CN92510367, CN92510374, CNO2510380, CNO2510392, CNO2510383, CNO2510386, CNO2510396, CNN2510412, CNN2510410, CNN2510427, CNN2510443, CNN2510444, CNN2510454, CNN2510485, CNN2510486, CND2510503, CND2510502, CND2510508, CND2510528, CND2510530, CND2510566, CND2510575, CND2510574, CN12610585, CN12610590, CN12610595, CN12610593, CN22610612, CN22610681, CN22610707, CN22610735, CN32610755, CN32610760, CN32610761, CN32610762, CN32610763, CN32610765, CN32610818, CN32610826, CN32610910, CN32610913, CN32610912, CN32610924, CN32610923, CN32610929, CN32610930, CN32610933, CN42610944, CN42610951, CN42610970, US42610994

Recalling firm:

Philips North America Llc

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

Recall #:

99361

Lot/product code:

Product Number: 860441. UDI: (01)00884838094833. Serial Numbers: US22520232, US32520244, US32520248, US42520323, US42520320, US42520300, US52520333, US52520332, US52520345, US52520382, US52520359, US52520390, US52520373, US52520412, US52520420, US52520426, US52520461, US62520469, US62520470, US62520474, US62520476, US62520483, US72520504, US72520518, US72520531, US62520499, US72520500, US72520648, US72520526, US72520524, US72520522, US72520517, US72520590, US72520547, US72520592, US82520720, US72520603, US72520640, US72520580, US72520666, US82520755, US82520752, US82520762, US72520662, US72520652, US72520664, US82520771, US82520844, US82520782, US82520774, US82520769, US82520777, US82520775, US82520855, US82520820, US82520823, US82520824, US82520744, US72520678, US82520822, US82520821, US82520726, US72520667, US72520670, US72520668, US82520848, US72520669, US92520885, US82520857, US82520851, US82520863, US92520881, US92520890, US92520901, US92520903, US92520894, US92520905, US92520906, US92520981, USO2521043, USO2521042, USO2521050, USO2521128, USO2521092, USO2521122, USO2521065, USN2521141, US92520990, USN2521132, USN2521144, USN2521149, USN2521130, USN2521179, USN2521150, USN2521161, USN2521163, USN2521164, USN2521160, USO2521072, USN2521175, USN2521170, USN2521176, USN2521185, USN2521206, USN2521211, USN2521214, USN2521213, USN2521196, USN2521226, USN2521223, USN2521249, USN2521215, USN2521224, USN2521246, USN2521243, USN2521235, USN2521221, USN2521222, USN2521342, USN2521198, USN2521254, USN2521252, USN2521294, USN2521286, USN2521258, USN2521257, USN2521256, USN2521307, USN2521288, USN2521287, USD2521394, USN2521289, USN2521300, USN2521296, USD2521365, USN2521302, USD2521427, USD2521407, USD2521436, USD2521433, USD2521448, USD2521440, USD2521475, USD2521430, USN2521308, USD2521362, USD2521374, USN2521309, USD2521355, US12621548, US12621550, US12621553, US12621671, US12621672, US12621629, US12621713, US12621712, US12621711, US12621710, US22621762, US22621763, US22621777, US22621787, US22621796, US22621859, US32621881, US32621887, US32621893, US32621905, US32621886, US32621884, US32621894, US32621906, US32621907, US32621909, US32621910, USD2521420, USD2521409, USD2521411, USD2521416, USD2521422, US32621911, US32621918, US32621912, US32621913, US32621936, US32622017, US32621923, US32621980, US32621953, US32621952, US32621950, US32621954, US32621895, US32622011, US32622018, US32622051, US32622023, US32622077, US32622078, US32622046, US42622153, US32622027, US32622053, US32622052, US32622076, US32622064, US42622108, US32622065, US42622129, US42622123, US42622110, US42622148, US42622113, US42622111, US42622154, US42622147, US42622139, US42622146, US42622116, US42622149, US42622150, US42622222, US42622188, US42622183, US42622187, US42622156, US42622184, CN72420050, CN82420071, CNO2420085, CNN2420093, CNN2420096, CNN2420111, CNN2420115, CND2420119, CND2420145, CND2420134, CND2420150, CND2420151, CND2420168, CND2420167, CND2420169, CND2420171, CN12520174, CN22520206, CN22520215, CN22520218, CN22520214, CN22520226, CN22520242, CN32520246, CN42520274, CN42520317, CN42520291, CN52520389, CN52520379, CN52520445, CN52520460, CN52520454, CN62520466, CN62520487, CN72520565, CN72520650, CN72520631, CN82520721, CN72520651, CN82520758, CN82520764, CN82520791, CN82520792, CN82520793, CN82520837, CN82520842, CN82520864, CN82520809, CN92520880, CN92520871, CN92520923, CN92520929, CN92520970, CN92520935, CN92520979, CN92520976, CNO2521015, CNO2520997, CNO2521008, CNO2521007, CNO2521026, CNO2521030, CNO2520998, CNN2521156, CNN2521212, USN2521219, CNN2521230, CNN2521283, CNN2521260, USN2521291, CNN2521346, CNN2521345, CNN2521344, CNN2521343, CND2521375, CND2521352, CND2521415, CND2521439, USD2521429, CND2521506, CN12621557, CND2521535, CND2521544, CN12621562, CN12621580, CN12621577, CN12621576, CN12621579, CN12621690, CN12621687, CN12621696, CN12621697, CN12621698, CN22621734, CN22621799, CN22621798, CN32621877, CN22621874, CN32621875, CN32621888, CN32621890, CN32621896, CN32621968, CN32621997, CN32622002, CN32621990, CN32621983, CN32622007, CN32622008, CN32622005, CN32622006, CN32622021, CN32622047, CN32622066, CN32622075, CN42622107, CN42622124, CN42622134, CN42622220, CN42622221

Recalling firm:

Philips North America Llc

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

Recall #:

H-1190-2026

Lot/product code:

Lot: CA1G24 Expiration: 08-2027

Recalling firm:

Mellish Island Corp

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

Recall #:

99402

Lot/product code:

Lot Code: Model No 1500-1030; UDI-DI 00840097513225; Lot Numbers A00030, A00065, A09828, A09830 Model No 1500-1035; UDI-DI 00840097513232; Lot Numbers A00064, A09829

Recalling firm:

restor3d Inc.

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

Recall #:

99439

Lot/product code:

DUI/DI 07325710000304, Serial/Lot Numbers: 21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.

Recalling firm:

Maquet Critical Care AB

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

Recall #:

99432

Lot/product code:

UDI-DI (each) 80080196314521, UDI-DI (case) 10080196314522, Lot Numbers: All lots produced between 10/27/2025 and 11/19/2025

Recalling firm:

Medline Industries, LP