Recalls affecting Nevada

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: 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: 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 #:

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 #:

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 #:

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 #:

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: B1018-496 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: B1018-440 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: B1018-340R UDI-DI Code: 15099590684112 Serial Numbers: 34020035 34020224 34030054

Recalling firm:

Beckman Coulter 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 #:

85376

Lot/product code:

All lots

Recalling firm:

Encore Medical, LP

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

Recall #:

D-0539-2020

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-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-0542-2020

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-0534-2020

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-0535-2020

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-0540-2020

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-0537-2020

Lot/product code:

all lots

Recalling firm:

Sanofi-Aventis U.S. LLC