Recalls affecting Washington

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

Recall #:

83852

Lot/product code:

Product Code: 114870; All Lot numbers; GTIN: 07332414115395. Device not distributed in the US.

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

85526

Lot/product code:

All lots

Recalling firm:

Ventana Medical Systems Inc

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

Recall #:

83852

Lot/product code:

Product Code: 115269 (GTIN: 07332414117702), 955542 GTIN: 07332414124236); All Lot numbers

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

83852

Lot/product code:

Product Code: 107493; All Lot numbers; GTIN: 07332414073718

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

84032

Lot/product code:

Codes: 73J1600836 73C1700518 73D1800018 73H1800233 73A1900664 73J1600837 73C1700842 73D1800019 73H1800234 73B1900436 73K1600114 73D1700008 73D1800020 73H1800235 73B1900437 73K1600115 73D1700009 73D1800558 73H1800236 73B1900438 73K1600290 73D1700010 73D1800559 73H1800240  73K1600515 73D1700068 73D1800560 73H1800496  73K1600814 73D1700069 73D1800561 73H1800497  73L1600097 73D1700313 73D1800562 73H1800498  73L1600098 73D1700314 73D1800563 73H1800499  73L1600099 73D1700315 73D1800564 73H1800500  73L1600100 73D1700496 73D1800565 73H1800501  73L1600101 73D1700497 73E1800526 73H1800502  73L1600274 73D1700574 73E1800527 73H1800639  73L1600275 73D1700575 73E1800528 73H1800640  73L1600276 73F1700209 73E1800529 73H1800641  73L1600277 73F1700210 73E1800530 73H1800642  73L1600278 73G1700345 73F1800263 73H1800643  73L1600279 73G1700346 73F1800264 73H1800820  73L1600280 73G1700347 73F1800265 73J1800298  73L1600540 73G1700720 73F1800266 73J1800299  73L1600792 73G1700721 73F1800267 73J1800300  73L1600793 73H1700095 73F1800268 73J1800301  73L1600794 73H1700096 73F1800269 73J1800302  73L1600795 73H1700097 73F1800270 73J1800303  73L1600796 73H1700098 73F1800486 73J1800304  73L1600797 73B1800105 73F1800487 73J1800305  73L1600798 73B1800106 73F1800759 73J1800306  73M1600217 73B1800188 73F1800760 73J1800718  73M1600218 73B1800189 73F1800761 73J1800719  73M1600219 73B1800190 73G1800089 73J1800720  73M1600220 73B1800192 73G1800520 73K1800055  73M1600281 73B1800216 73G1800521 73K1800057  73M1600282 73B1800217 73G1800522 73K1800058  73A1700205 73C1800125 73G1800525 73K1800691  73A1700206 73C1800126 73G1800726 73K1800694  73A1700207 73C1800127 73G1800727 73K1800700  73A1700348 73C1800128 73G1800728 73K1800701  73A1700349 73C1800129 73G1800729 73K1800702  73B1700226 73C1800130 73G1800730 73K1800703  73B1700276 73C1800131 73G1800731 73M1800021  73B1700486 73C1800132 73G1800877 73M1800022  73B1700487 73D1800013 73G1800878 73M1800023  73C1700335 73D1800014 73H1800138 73M1800024  73C1700360 73D1800015 73H1800139 73M1800025  73C1700361 73D1800016 73H1800231 73A1900662  73C1700362 73D1800017 73H1800232 73A1900663

Recalling firm:

Teleflex Medical

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

Recall #:

83852

Lot/product code:

Product Code: 113081; All Lot numbers; GTIN: 07332414105266

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

83852

Lot/product code:

Product Code: 6023014700; All Lot numbers; GTIN: 07332414073718.

Recalling firm:

Baxter Healthcare Corporation

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

Recall #:

86941

Lot/product code:

Serial # range: HF-4258BKHA0001 to HF4258RDHK0352 (Purchased before April 4th,2019)

Recalling firm:

Nova Ortho-Med Inc

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

Recall #:

84054

Lot/product code:

All

Recalling firm:

Teleflex Medical

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

Recall #:

84054

Lot/product code:

All

Recalling firm:

Teleflex Medical

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

Recall #:

84054

Lot/product code:

All

Recalling firm:

Teleflex Medical

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

Recall #:

84028

Lot/product code:

All systems using Software version VG2.3.1 and lower

Recalling firm:

Draegar Medical Systems, Inc.

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

Recall #:

85346

Lot/product code:

Panther Fusion Extraction Reagent-S Lot number: 258402 Panther Fusion Capture Reagent-S Lot number: 257472 Panther Fusion Enhancer Reagent-S Lot number: 257473

Recalling firm:

Hologic, Inc

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

Recall #:

85551

Lot/product code:

Lot/Batch Numbers: 74A1900703, 74D1802540, 74E1800978, 74F1801413, 74G1800896, 74H1800162, 74K1801738, 74K1802909, 74L1800502

Recalling firm:

TELEFLEX MEDICAL INC

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

Recall #:

85551

Lot/product code:

Lot/Batch Numbers: 74A1900698, 74C1902955, 74C1900349, 74C1900137, 74E1802338, 74G1802129, 74H1802488, 74K1800901, 74K1801734, 74L1802219

Recalling firm:

TELEFLEX MEDICAL INC

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

Recall #:

84178

Lot/product code:

Product Code: 494A/494A-IMC; Lot Number: 190123-59; date of manufacture: 03/04/2019

Recalling firm:

CP Medical Inc

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

Recall #:

90087

Lot/product code:

Catalog Number: B1018-284 UDI-DI Code: 15099590658687 Serial Numbers: 39610007 39610008 39610009 39610010 39610011 39610012 39610013

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

90087

Lot/product code:

Catalog Number: B1018-440 UDI-DI Code: 15099590690885 Serial Numbers: 44010026 44010027 44010028 44010029 44010030 44010031 44010032 44010033 44010035 44010036 44010037 44010038 44010040 44010041 44010042 44010043 44010044 44010045 44010046 44010047 44010048 44010049 44010050 44010051 44010052 44010053 44010054 44010055 44010056 44010057 44010058 44010059 44010060 44010061 44010063 44010064 44010065 44010066 44010067 44010068

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

90087

Lot/product code:

Catalog Number: B1018-496 UDI-DI Code: 15099590690892 Serial Numbers: 49610039 49610040 49610041 49610042 49610043 49610044 49610045 49610046 49610047 49610048 49610050 49610051 49610052 49610053 49610054 49610055 49610056 49610057 49610058 49610059 49610060 49610062 49610063 49610064 49610065 49610066 49610067 49610068 49610069 49610070 49610071 49610072 49610073 49610074 49610075 49610078 49610079 49610080 49610081 49610082 49610083 49610084 49610085 49610086 49610087 49610088 49610089 49610090 49610091

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

90087

Lot/product code:

Catalog Number: B1018-283 UDI-DI Code: 1509959065866 Serial Numbers: 34010003 34010004 34010005 34010006 34010007 34010008 34010009 34010010 34010011 34010012 34010013 34010014 34010015 34010016 34010017 34010018 34010019 34010020 34010021 34010022 34010023 34010024

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

90087

Lot/product code:

Catalog Number: B1018-396R UDI-DI Code: 15099590684129 Serial Numbers: 39620362 39620406 3967731 3967914

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

90087

Lot/product code:

Catalog Number: B1018-340R UDI-DI Code: 15099590684112 Serial Numbers: 34020035 34020224 34030054

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

D-0536-2020

Lot/product code:

all lots

Recalling firm:

Sanofi-Aventis U.S. LLC

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

Recall #:

D-0544-2020

Lot/product code:

all lots

Recalling firm:

Sanofi-Aventis U.S. LLC

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

Recall #:

D-0543-2020

Lot/product code:

all lots

Recalling firm:

Sanofi-Aventis U.S. LLC