Recalls affecting New Hampshire

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

Recall #:

99301

Lot/product code:

DYNJ61206J UDI-DI 10198459488597 Lots 25IMF461 25LMG907

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-0659-2026

Lot/product code:

Lot #: AE3102, 031926L01, 032026A01, Exp 11/30/2026; AE5052, 052026G01, Exp 04/30/2028.

Recalling firm:

Asclemed USA Inc.

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

Recall #:

99323

Lot/product code:

1) Pack Number AMS12206, UDI B098AMS122060, Lot Numbers: 201002, 205119, 206649, 211870, 215233, 217552, 218967, 219166, 222076, 224914, 227000, 228485, 230336, 231348, 232214, 238290, 239795, 241802. 2) Pack Number AMS15517, UDI B098AMS155170, Lot Numbers: 215924, 218494, 235207, 241105. 3) Pack Number AMS15863A, UDI B098AMS15863A0, Lot Numbers: 229370, 235320, 235699, 237597, 239311, 241458.

Recalling firm:

Windstone Medical Packaging, Inc.

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

Recall #:

D-0656-2026

Lot/product code:

Lot # D2401522, Exp Date: 06/2026.

Recalling firm:

ACCORD HEALTHCARE, INC.

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

Recall #:

99214

Lot/product code:

Material Number: 11097536. UDI-DI: 00630414220505. All Lot Numbers.

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

D-0662-2026

Lot/product code:

Lot #: 7000612A, Exp. Date 1/2028

Recalling firm:

ONESOURCE SPECIALTY PHARMA LIMITED

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

Recall #:

D-0610-2026

Lot/product code:

[100 tablet bottle] Batch RISA24001; [1000 tablet bottle] Batch RISB24002; Exp. 04/2027

Recalling firm:

Inventia Healthcare Limited

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

Recall #:

99279

Lot/product code:

UDI-DI: 00840682115278; System IDs: 419383DP3, 773792XR200, 856355OPT, FEB520100

Recalling firm:

GE Medical Systems, LLC

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

Recall #:

99193

Lot/product code:

Product Code 3032, UDI 10381780268468; Product Code 3055, UDI 10381780268505; Product Code 3069, UDI 10381780268512; Product Code 3076, UDI 10381780268529; Product Code 3086, UDI 10381780268536; Product Code 3092, UDI 10381780268550; Product Code 3093, UDI 10381780268567; Product Code 3096, UDI 10381780268581; Product Code 3098, UDI 10381780268598; Product Code 3099, UDI 10381780268604; Product Code 3133, UDI 10381780268680; Product Code 3137, UDI 10381780268697; Product Code 3142, UDI 10381780268710; Product Code 3146, UDI 10381780268734; Product Code 3148, UDI 10381780268758; Product Code 3176, UDI 10381780268826; Product Code 3177, UDI 10381780268833; Product Code 3185, UDI 10381780268857; Product Code 3201, UDI 10381780268871; Product Code 3203, UDI 10381780268888; Product Code 3216, UDI 10381780268895; Product Code 3217, UDI 10381780268901; Product Code 3218, UDI 10381780268918; Product Code 3219, UDI 10381780268925; Product Code 3220, UDI 10381780268932; Product Code 3274, UDI 10381780268994; Product Code 3312, UDI 10381780269038; Product Code 3335, UDI 10381780269045; Product Code 3336, UDI 10381780269052; Product Code 3342, UDI 10381780269076; Product Code 3343, UDI 10381780269083; Product Code 3391, UDI 10381780269168; Product Code 3398, UDI 10381780269212; Product Code 3424, UDI 10381780269243; Product Code 3426, UDI 10381780269250; Product Code 3483, UDI 10381780269267; Product Code 3485, UDI 10381780269274; Product Code 3520, UDI 10381780282273; Product Code 3529, UDI 10381780269281; Product Code 3530, UDI 10381780269298; Product Code 3531, UDI 10381780269304; Product Code 3532, UDI 10381780269311; Product Code 3533, UDI 10381780269328; Product Code 3534, UDI 10381780269335; Product Code 3535, UDI 10381780269342; Product Code 3536, UDI 10381780269359; Product Code 3537, UDI 10381780269366; Product Code 3555, UDI 10381780269373; Product Code 3557, UDI 10381780269380; Product Code 3565, UDI 10381780269397; Product Code 3570, UDI 10381780269403; Product Code 3575, UDI 10381780269410; Product Code 3586, UDI 10381780269427; Product Code 3588, UDI 10381780269434; Product Code 3590, UDI 10381780269441; Product Code 3592, UDI 10381780269458; Product Code 3593, UDI 10381780269465; Product Code 3594, UDI 10381780269472; Product Code 3595, UDI 10381780269489; Product Code 3596, UDI 10381780269496; Product Code 3597, UDI 10381780269502; Product Code 3601, UDI 10381780269519; Product Code 3602, UDI 10381780269526; Product Code 3603, UDI 10381780269533; Product Code 3604, UDI 10381780269540; Product Code 3605, UDI 10381780269557; Product Code 3610, UDI 10381780269564; Product Code 3614, UDI 10381780269571; Product Code 3616, UDI 10381780269588; Product Code 3618, UDI 10381780269595; Product Code 3620, UDI 10381780269601; Product Code 3622, UDI 10381780269618; Product Code 3623, UDI 10381780269625; Product Code 3624, UDI 10381780269632; Product Code 3626, UDI 10381780269649; Product Code 3630, UDI 10381780269656; Product Code 3631, UDI 10381780269663; Product Code 3635, UDI 10381780269670; Product Code 3640, UDI 10381780269687; Product Code 3647, UDI 10381780269694; Product Code 3650, UDI 10381780269700; Product Code 3654, UDI 10381780202936¿; Product Code 3700, UDI 10381780269717; Product Code 3720, UDI 10381780269724; Product Code 3732, UDI 10381780269731; Product Code 3740, UDI 10381780269748; Product Code 3759, UDI 10381780269755; Product Code 3761, UDI 10381780269762; Product Code 3763, UDI 10381780269779; Product Code 3765, UDI 10381780269786; Product Code 3772, UDI 10381780269793; Product Code 3774, UDI 10381780269809; Product Code 3780, UDI 10381780269816; Product Code 3782, UDI 10381780269823; Product Code 3784, UDI 10381780269830; Product Code 3786, UDI 10381780269847; Product Code 3788, UDI 10381780269854; Product Code 3790, UDI 10381780269861; Product Code 3792, UDI 10381780269878; Product Code 3794, UDI 10381780269885; Product Code 3796, UDI 10381780269892; Product Code 3798, UDI 10381780269908; Product Code 3800, UDI 10381780269915; Product Code 3812, UDI 10381780269960; Product Code 3814, UDI 10381780269977; Product Code 3816, UDI 10381780269984; Product Code 3824, UDI 10381780270027; Product Code 3842, UDI 10381780270034; Product Code 3848, UDI 10381780270041; Product Code 3860, UDI 10381780270089; Product Code 3862, UDI 10381780270096; Product Code 3864, UDI 10381780270102; Product Code 3870, UDI 10381780270133; Product Code 3872, UDI 10381780270140; Product Code 3874, UDI 10381780270157; Product Code 3886, UDI 10381780270218; Product Code 3888, UDI 10381780270225; Product Code 3890, UDI 10381780270232; Product Code 3892, UDI 10381780270249; Product Code 3900, UDI 10381780270256; Product Code 3909, UDI 10381780270294; Product Code 3910, UDI 10381780270300; Product Code 3911, UDI 10381780270317; Product Code 3914, UDI 10381780270324; Product Code 3915, UDI 10381780270331; … (truncated, 26108 characters total — see the official FDA record for the full value)

Recalling firm:

Integra LifeSciences Corp. (NeuroSciences)

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

Recall #:

99106

Lot/product code:

UDI/DI: 04953170441271, Lot Numbers: H2530 or later

Recalling firm:

Olympus Corporation of the Americas

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

Recall #:

99126

Lot/product code:

Model Number: 867232. UDI-DI: (01)00884838102842. Software Version Number: 4.0.0.0. Serial Numbers: US001A002F, US001A00AW, US001A00C9, US001A00EW, US001A00F0, US001A00GM, US001A00N4, US001A00PB, US001A00PZ, US001A00R1, US001A00UE, US001A00VU, US001A00Z4, US001A013T, US001A018A, US001A018R.

Recalling firm:

Philips North America Llc

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

Recall #:

99279

Lot/product code:

UDI-DI: 00840682122351 and 00840682123686; System IDs: 252847PP249, 281MSL2402, 291OPTI1, 312CCHSUPER7, 318487OPTIMA1, 360744OPT2402, 501686OPTI1, 504826XR241, 519941XR240A, 540776ODP3, 541472M4, 602344240C, 706291BEE9, 713799XR240, 770836BEE2, 813872OPT11, 813872OPT9, 843724OPT1, 843847OPT240, 870239OPT2, 905522AMX240, 973625DIG4, DF2402001002WK, SA1013MM13

Recalling firm:

GE Medical Systems, LLC

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

Recall #:

99279

Lot/product code:

UDI-DI: 00840682115261; System IDs: 05249MOB02.OLD, 205820DP1, 228818XR220, 229276M1, 240566P1, 301295OPTIMA2, 303788SBOPT1, 314251P5, 352LEEDP1, 386FLGDPXR3, 417347DPORT1, 512SAMCSB, 516632OPTIMA2, 540981ODP7, 563264OPT, 601445DP1, 615338HDP01, 661949DP2, 713441OPCDX1, 717657OPT1, 718206OPT240A, 727848SB1, 732321DP1, 757736DP3, 813302OPT1, 828213DXP1, 828286OPT1, 843847220D, 850070941, 865545DP3, 915821OPT1, 941342OP221, 972566XR220E, 985447TM4, SA1208MM05, SB2201700085WK, XR1034798WK7, XR1037005WK4

Recalling firm:

GE Medical Systems, LLC

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

Recall #:

D-0595-2026

Lot/product code:

Lots: a) TL8K, YH9X, YH9Y, Exp. Date. 30Nov2028; b) X78N, Exp. Date 30Nov2028.

Recalling firm:

Haleon US Holdings LLC

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

Recall #:

D-0627-2026

Lot/product code:

Lots PO062402, Exp Date 6/30/2026, PO072401, Exp Date 7/30/2026, PO092401, Exp Date 9/30/2026, PO102401, Exp Date 10/31/2026 & PO102402, Exp Date 10/31/2026.

Recalling firm:

Elevate Oral Care

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

Recall #:

D-0615-2026

Lot/product code:

Lot #: 1138203, 1142065, Exp. Date 07/31/2026; 1145151, 1145152, 1145153, Exp. Date 2/28/2027; 1148908, 1148909, Exp. Date 05/31/2027; 1162845, 1162846, Exp. Date 11/30/2027; 1166471, 1166472, 1166473, Exp. Date 05/31/2028; 1170615, Exp. Date 08/31/2028

Recalling firm:

Amgen, Inc.

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

Recall #:

D-0655-2026

Lot/product code:

Lots: a) HA00937, HA00939, HA00941, HA00971, H00973, HA00975, Expires: 7/31/2026; HA00987, HA00989, HA00991, HA01010, HA01012, HA01014, HA01016, HA01048, Expires: 8/31/2026; HA01120, HA01137, HA01129, HA01138, HA01133, Expires: 9/30/2026; HA01148, HA01196, HA01198, HA01200, HA01206, HA01208, HA01210, HA01212, HA01214, HA01216, HA01218, HA01220, Expires: 10/31/2026; HA01236, HA01238, HA01240, HA01244, HA01246, HA01248, HA01261, HA01263, HA01265, HA01267, HA01278, HA01280, HA01282, HA01284, HA01288, HA01290, HA01292, HA01298, Expires: 11/30/2026; HB00002, HB00004, HB00006, HB00017, HB00019, HB00021, HB00023, HB00025, HB00031, HB00033, HB00035, HB00037, HB00039, HB00041, HB00043, Expires: 12/31/2026; HB00049, HB00051, HB00076, HB00078, HB00080, HB00082, HB00084, Expires: 1/31/2027; HB00128, HB00130, HB00132, HB00134, HB00157, HB00159, HB00161, HB00196, HB00198, HB00200, Expires: 2/28/2027; HB00224, HB00226, HB00228, HB00230, HB00240, HB00242, Expires: 3/31/2027; HB00416, HB00417, HB00419, HB00439, HB00441, HB00443, HB00463, HB00465, Expires: 5/31/2027; HB00561, Expires: 6/30/2027; HB00569, HB00657, HB00659, HB00663, HB00671, HB00673, HB00675, HB00677, HB00679, Expires: 10/31/2027; HB00747, HB00749, HB00751, HB00753, Expires: 11/30/2027; HB00761, HB00763, HB00765, HB00783, HB00785, HC00002, HC00004, HC00006, HC00018, HC00020, HC00028, Expires: 12/31/2027; HC00030, HC00032, Expires: 1/31/2028; HC00056, HC00058, HC00062, HC00064, HC00073, HC00075, HC00079, HC00081, HC00083, Expires: 2/29/2028; HC00091, Expires: 3/31/2028; b) HA00945, HA00947, HA00949, Expires: 7/31/2026; HA01160, HA01162, HA01164, Expires: 10/31/2026; HA01234, HA01300, HA01302, Expires: 11/30/2026; HB00053, HB00055, HB00057, Expires: 1/31/2027; HB00107, HB00109, HB00111, HB00151, HB00153, HB00155, Expires: 2/28/2027; HB00386, HB00388, HB00390, HB00445, HB00447, Expires: 5/31/2027; HB00549, HB00551, HB00553, HB00555, Expires: 6/30/2027; HB00700, HB00702, Expires: 10/31/2027; HB00771, Expires: 11/30/2027; HC00008, HC00010, Expires: 12/31/2027; HC00034, HC00038, HC00054, HC00060, Expires: 1/31/2028; c) HA00951, HA00953, HA00955, Expires: 7/31/2026; HA01188, HA01190, HA01192, Expires: 10/31/2026; HA01304, Expires: 11/30/2026; HB00113, HB00115, Expires: 1/31/2027; HB00166, HB00168, Expires: 2/28/2027; HB00392, HB00394, HB00396, Expires:5/31/2027; HB00545, HB00547, Expires: 6/30/2027; HB00704, Expires: 10/31/2027; HB00773, Expires: 11/30/2027; HC00012, HC00014, Expires: 12/31/2027; HC00066, HC00068, Expires: 2/29/2028.

Recalling firm:

Lupin Pharmaceuticals Inc.

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

Recall #:

99213

Lot/product code:

Lot 0853293604 UDI-DI 03573026634551 Product is not registered in the US. OUS only.

Recalling firm:

Biomerieux Inc

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

Recall #:

D-0614-2026

Lot/product code:

Lot #: 1157055, Exp. Date 1/31/2028

Recalling firm:

Amgen, Inc.

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

Recall #:

D-0582-2026

Lot/product code:

Lot: 241180C, Exp. Date April 2027.

Recalling firm:

Breckenridge Pharmaceutical, Inc.

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

Recall #:

D-0626-2026

Lot/product code:

Lot: A253999, A254000, Expires: 09/30/2027.

Recalling firm:

Annora Pharma Private Limited

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

Recall #:

99260

Lot/product code:

Model/Catalog Number: 96102 DisplayPort Splitter Part Number: 010-1975-00 UDI-DI codes: 1084152212706 10841522100345 Serial Numbers: Pending

Recalling firm:

Spacelabs Healthcare, Inc.

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

Recall #:

D-0612-2026

Lot/product code:

a) Lot # 1138901, Exp. Date 08/31/2026; 1149846, Exp. Date 04/30/2027 b) Lot #1138201, 1138202, 08/31/2026, 1138900, 1141143, Exp. Date 08/31/2026; 1140280, 1140281, 1142063, Exp. Date 10/31/2026; 1142062, 1142942, 1142943, Exp. Date 11/30/2026; 1144081, 1144104, Exp. Date 12/31/2026; 1146373, 1146374, Exp. Date 01/31/2027; 1147491, 1147492, 1149843, Exp. Date 03/31/2027; 1151113, 1151890, 1153401, Exp. Date 07/31/2027; 1151114, 1151115, Exp. Date 09/30/2027; 1152412, 1153399, 1153400, Exp. Date 06/30/2027; 1155834, 1155835, Exp. Date 04/30/2027; 1155836, Exp. Date 09/30/2027; 1158480, 1158481, 1158482, Exp. Date 10/31/2027; 1160354, 1160355, Exp. Date 03/31/2028; 1161593, 1161594, 1161595, Exp. Date 04/30/2028; 1164097, 1164098, 1164099, Exp. Date 06/30/2028; 1165078, 1165079, Exp Date 07/31/2028; 1165080, Exp. Date 02/29/2028;1168005, 1168006, 1168007, Exp. Date 09/30/2028; 1169288, 1169289, Exp. Date 10/31/2028; 1172885, Exp. Date 12/31/2028.

Recalling firm:

Amgen, Inc.

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

Recall #:

D-0583-2026

Lot/product code:

Lot: a) 241074C, Exp. Date May 2027; 240317, 240318, 240315C, 240373C, 240370C, 240375C, 240413C, Exp. Date February 2027; 240316,Exp. Date January 2027; 232311, Exp. Date November 2026; b) 240978C, 241052C, Exp. Date April 2027.

Recalling firm:

Breckenridge Pharmaceutical, Inc.

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

Recall #:

D-0613-2026

Lot/product code:

Lot#: 1156858, Exp. Date 12/31/2027.

Recalling firm:

Amgen, Inc.