Recalls affecting Wyoming

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-2310-2017

Lot/product code:

ALL

Recalling firm:

Pinnacle Foods, LLC

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

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 #:

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: 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: 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 #:

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 #:

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 APOLLO 1V+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 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 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 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 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 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 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 UL Station

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-3013-XX; 0998-UC-3013-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-UC-0446HXX; 0998-UC-0479HXX

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-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 #:

80583

Lot/product code:

Product Number 89140.0105, Lot Number 4500197481

Recalling firm:

Richard Wolf GmbH

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

Recall #:

79075

Lot/product code:

UDI 10884521706590, Lot codes: S6MG006PX,S6MG009PX,S6MG013PX,S6MG020PX,S7AG011X,S7AG012X,S7BG008X,S7CG003X,S7DG003X,S7DG009X,S7FG001X,S7FG002X,S7FG005X,S7FG008X

Recalling firm:

Covidien LLC

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

Recall #:

79075

Lot/product code:

UDI 10884521189546, Lot codes: S5LG003PX,S5MG016PX,S5MG018PX,S6AG004X,S6AG005X,S6AG007X,S6BG004X,S6BG011X,S6BG015PX,S6BG017X,S6CG002X,S6CG008X,S6CG014X,S6CG015X,S6CG016X,S6DG002X,S6DG005X,S6DG007X,S6DG010X,S6EG004X,S6EG006X,S6EG008X,S6FG005X,S6FG008X,S6GG007X,S6GG010X,S6HG001X,S6HG003PX,S6HG008PX,S6HG009PX,S6HG012X,S6JG001X,S6KG003X,S6KG005PRX,S6KG005PX,S6KG009X,S6KG016X,S6LG002X,S6MG003X,S6MG018X,S7AG003X,S7BG012PCX,S7CG004X,S7CG006X,S7CG008PCX,S7CG010PCX,S7CG017X,S7DG002X,S7DG005X,S7EG006X,S7FG010PX

Recalling firm:

Covidien LLC

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

Recall #:

79075

Lot/product code:

UDI 10884521706606, Lot codes: S6MG007PX,S6MG010PX,S6MG016PX,S7AG002PX,S7BG005X,S7BG009X,S7DG004X,S7FG006X

Recalling firm:

Covidien LLC