Recalls affecting Alaska

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

Recall #:

98197

Lot/product code:

UDI/DI 10198459156991 (EA) 40198459156992 (CS), Lot Number 25EBM426

Recalling firm:

Medline Industries, LP

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

Recall #:

98128

Lot/product code:

400010401 (US), Software Versions: 1.0.2; 400011001 (Philippines), Software Versions: 1.0.0

Recalling firm:

ICU Medical, Inc.

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

Recall #:

98109

Lot/product code:

Model Number: 722010; System Product Name: Allura Xper FD10; UDI-DI: 00884838059030; Serial Numbers: 764, 1396, 728, 980, 782, 125, 1096, 661, 225, 1055, 1185, 368, 743, 1006, 570, 901, 552, 973, 795, 888, 1140, 781, 1060, 354, 186, 516, 517, 64, 386, 387, 530, 996, 964, 1265, 525, 307, 1189, 98, 774, 935, 721, 254, 1008, 1213, 1273, 66, 156, 304, 1422, 388, 235, 236, 1066, 1090, 549, 689;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98274

Lot/product code:

Lot Code:W4904253, W4886945, W4880750 UDI: 10827002223018

Recalling firm:

Wilson-Cook Medical Inc.

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

Recall #:

98128

Lot/product code:

400020401 (US), Software Versions: 1.1.1, 1.1.2, 1.1.3, 1.1.4 400021001 (Philippines), Software Versions: 1.1.0

Recalling firm:

ICU Medical, Inc.

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

Recall #:

98208

Lot/product code:

Lot Code: Lot/Serial Number(s) 0004306540 0004316209 0004328895 0004329080 0004330876 0004331254 0004332994 0004338228 0004338229 0004338230 0004339717 UDI-DI Each-10889483588970 Case-30889483588974

Recalling firm:

SunMed Holdings, LLC

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

Recall #:

D-0397-2026

Lot/product code:

All codes; Exp 12/31/2029

Recalling firm:

StuffbyNainax

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

Recall #:

D-0300-2026

Lot/product code:

Lot # CB2505159A, CB2505160A, Exp Date: 04/2027; Lot # CB2505161A, Exp Date: 05/2027

Recalling firm:

NOVADOZ PHARMACEUTICALS LLC

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

Recall #:

98163

Lot/product code:

Reference Number: 00615. UDI: (01)03607450006155(11)240531(17)260531(10)271288(241)00615. Lot Number: 271288.

Recalling firm:

Diagnostica Stago, Inc.

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

Recall #:

98109

Lot/product code:

Model Number: 722003; System Product Name: Allura Xper FD10; UDI-DI: N/A; Serial Numbers: 1232, 967, 746, 1276, 232, 385, 1663, 1189, 81, 700, 167, 1072, 994, 150, 135, 1268, 168, 855, 213, 60, 471, 153, 319, 1159, 162, 180, 142, 1205, 719, 926, 426, 1413, 798, 65, 1165, 1658, 1193, 1778, 2933, 1585, 1380, 1706, 1613, 1685, 1297, 1388, 1522, 1238, 1416, 1448, 536, 1090, 1662, 1083, 1433, 1399, 62, 943, 249, 1227, 163, 1121, 1119, 889, 861, 1649, PP0200000118, 804, 1527, 468, 1593, 1198, 1022, 708, 1054, 865, 744, 1760, 936, 782, 953, 1035, 1058, 179, 1254, 1112, 389, 1560, 1660, 1013, 25, 215, 27;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98208

Lot/product code:

Lot Code: Lot/Serial Number(s) 0004312284 0004314503 0004333110 UDI-DI Each-10889483589151

Recalling firm:

SunMed Holdings, LLC

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

Recall #:

98109

Lot/product code:

Model Number: 722002; System Product Name: Allura Xper FD10F; UDI-DI: N/A; Serial Numbers: 61, 56, 27, 81, 25, 85, 20, 21, 84, 50, 31, 40;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722027; System Product Name: Allura Xper FD10/10; UDI-DI: 00884838054196; Serial Numbers: 298, 246, 146, 170, 238, 162, 7, 99, 81, 126, 55, 86, 6, 259, 205, 60, 57, 63, 145, 182, 48, 278;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722028; System Product Name: Allura Xper FD20; UDI-DI: 00884838054202; Serial Numbers: 893, 614;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98208

Lot/product code:

Lot Code: Lot/Serial Number(s) 0004325583 0004329077 0004329078 0004329079 0004331255 0004333368 0004335537 0004338439 0004340824 UDI-DI Each-10889483588963 Case-30889483588967

Recalling firm:

SunMed Holdings, LLC

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

Recall #:

98109

Lot/product code:

Model Number: 722026; System Product Name: Allura Xper FD10; UDI-DI: 00884838054189; Serial Numbers: 969, 223, 648, 664, 622, 931, 128, 616, 497, 769, 143, 881, 809, 18, 326, 794, 174, 804, 424, 587, 172, 911, 294, 569, 141, 161, 182, 928, 960, 858, 494, 628, 749, 968, 17, 273, 43, 203, 546, 104, 430, 575, 180, 594, 359, 723, 779, 632, 183, 330, 726, 637, 300, 429, 810, 995, 293, 296, 573, 917, 695, 676, 913, 274, 734, 520, 27, 940, 597, 598, 301, 818, 916, 328, 912, 691, 410, 873, 868, 816, 732, 147, 742, 651, 919, 89, 918, 346, 250, 755, 199, 255, 524, 256, 623;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722011; System Product Name: Allura Xper FD10/10; UDI-DI: 00884838059047; Serial Numbers: 268, 205, 213, 89, 293, 294, 116, 272, 113, 152, 112, 139, 141, 111, 81, 66, 46, 153, 115, 114, 274;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722001; System Product Name: Allura Xper FD10C; UDI-DI: N/A; Serial Numbers: 166, 181, 153, 274, 296, 267, 206, 247, 161, 282, 213, 284, 103, 199, 129, 95, 299, 30, 235, 221, 348, 283, 276, 253, 1100, 78, 229, 232, 159, 177, 219, 217, 205, 3, 89, 101, 295, 305;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722023; System Product Name: Allura Xper FD20 OR Table; UDI-DI: 00884838059085; Serial Numbers: 103, 10, 85, 125;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722008; System Product Name: Allura Xper FD20 Biplane; UDI-DI: N/A; Serial Numbers: 296, 245, 141, 260, 13, 410, 196, 476, 488, 290, 339, 474, 383, 530, 722008530, 223, 468, 63;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722005; System Product Name: Allura Xper FD10/10; UDI-DI: N/A; Serial Numbers: 93, 269, 530, 306, 307, 247, 53, 401, 141, 531, 184, 75, 276, 36;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722029; System Product Name: Allura Xper FD20/10; UDI-DI: 00884838054219; Serial Numbers: 30, 81, 80, 47;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722012; System Product Name: Allura Xper FD20; UDI-DI: 00884838059054; Serial Numbers: 2942, 1515, 1189, 1594, 535, 1964, 2156, 2742, 2092, 1673, 1803, 1655, 2020, 1973, 2037, 1853, 2098, 1248, 1082, 1576, 1057, 1129, 646, 930, 1421, 462, 203, 627, 2005, 1428, 353, 288, 191, 1994, 1802, 156, 853, 1283, 1956, 2361, 1980, 872, 931, 1295, 2513, 1090, 1374, 468, 1822, 812, 1379, 1817, 1580, 1050, 309, 144, 1841, 1845, 1468, 558, 1968, 1959, 2168, 1168, 1562, 967, 2114, 47, 167, 2091, 2053, 604, 603, 217, 2918, 373, 850, 1820, 1821, 1619;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722013; System Product Name: Allura Xper FD20 Biplane; UDI-DI: 00884838059061; Serial Numbers: 601, 230, 370, 27, 320, 193, 60, 373, 560, 400, 549, 506, 381, 382, 132, 169, 233, 236, 243, 526, 447, 163, 403;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

98109

Lot/product code:

Model Number: 722038; System Product Name: Allura Xper FD20/20; UDI-DI: 00884838054226; Serial Numbers: 11, 117, 110, 134, 64, 90, 124, 72;

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.