Recalls affecting Louisiana

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

Recall #:

F-2308-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2294-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2292-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2293-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

Recall #:

F-2409-2017

Lot/product code:

Exp 09/19/2017, UPC 8-96211-00235-9

Recalling firm:

Global Garlic, Inc.

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

Recall #:

77330

Lot/product code:

Product Code 5-15103 - Lot Number 73J1600218, 73K1600376, 73K1600587, 73L1600158, 73M1600275, 73A1700733;

Recalling firm:

Teleflex Medical

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

Recall #:

F-2410-2017

Lot/product code:

Exp 06/17/2017, no UPC

Recalling firm:

Global Garlic, Inc.

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

Recall #:

D-0793-2017

Lot/product code:

Lot#: 7ZP0634, 7ZP0810, 7ZP0990, Exp. 5/18

Recalling firm:

GlaxoSmithKline, LLC

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

Recall #:

77469

Lot/product code:

Product code 317-07, Lot Number NGAR0462, Device Listing Number D234021.

Recalling firm:

C.R. Bard, Inc.

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

Recall #:

77603

Lot/product code:

Serial No. 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 238, 240, 242, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 290, 292, 294, 296, 298, 300, 302, 304, 308, 312, 320, 334, 336, 338, 340, 342, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 378, 380, 382, 384, 386, 388, 396, 400, 402, 406, 408, 418, 420, 422, 424, 426, 428, 432, 434, 438, 440, 442, 444, 450, 452, 454, 456, 460, 462, 464, 468, 478, 480, 482, 484, 486, 488, 490, 492, 498, 502, 504, 516, 526, 530, 536, 544, 546, 548, 550, 554, 556, 558, 560, 562, 564, 570, 572, 574, 576, 580, 582, 584, 586, 588, 590, 598, 604, 612, 614, 628, 632, 636, 640, 642, 646, 650, 654, 660, 662, 666, 668, 674, 676, 684, 686, 692, 694, 696, 698, 700, 702, 704, 706, 712, 718, 720, 726, 728, 730, 732, 734, 736, 738, 742, 744, 746, 770, 784, 794, 796, 808, 810, 814, 816, 818, 820, 824, 834, 858, 860, 864, 866, 868, 870, 874, 878, 886, 892, 314, 316, 448, 538, 594, 622, 712, 778.

Recalling firm:

Leica Microsystems, Inc.

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

Recall #:

77801

Lot/product code:

Lot Numbers: 507830, 871270, 959670

Recalling firm:

Encore Medical, Lp

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

Recall #:

77801

Lot/product code:

Lot Numbers: 508250, 959680

Recalling firm:

Encore Medical, Lp

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

Recall #:

77801

Lot/product code:

Lot Numbers: 508220, 189680, 199200, 310390, 424730, 668130, 668150, 871240, 959720

Recalling firm:

Encore Medical, Lp

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

Recall #:

77801

Lot/product code:

Lot Numbers: 189690, 189760, 199180, 424740, 508240, 560290, 595660, 638280, 786630, 959650, 959700

Recalling firm:

Encore Medical, Lp

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

Recall #:

81217

Lot/product code:

Serial Numbers: 309658, 310007, 319209, 319822, 319823, 319824, 319825, 319826, 319827, 319829, 319830, 319831, 330695, 330696, 330697, 331862, 331914, 332387, 332586, 332587, 332589, 333755, 333761, 333762, 334833, 342515, 342518, 342523, 345084, 345085

Recalling firm:

R82 A/S

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

Recall #:

79697

Lot/product code:

Model Trixel C02 Laser

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model Diode Laser

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model UL C02 Laser

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model Nice Station Light Based Platform

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model Trixel 11 C02 Laser

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model UL Station

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model Apollo V + Medical Platform

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

79697

Lot/product code:

Model APOLLO 1V+Medical Platform

Recalling firm:

Beijing Syntech Laser Co., Ltd

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

Recall #:

77877

Lot/product code:

0998-XX-3023-XX; 0998-UC-3023-XX

Recalling firm:

Maquet Datascope Corp - Cardiac Assist Division

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

Recall #:

77877

Lot/product code:

0998-XX-3013-XX; 0998-UC-3013-XX

Recalling firm:

Maquet Datascope Corp - Cardiac Assist Division