Recalls affecting Connecticut

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: B1018-340R 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: B1018-440 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: B1018-283 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.

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

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-0538-2020

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-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-0545-2020

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-0541-2020

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-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-0543-2020

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

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

Recall #:

84191

Lot/product code:

Lot Numbers: 0009665221 0009709452 0009960538

Recalling firm:

Medtronic Navigation, Inc.

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

Recall #:

84249

Lot/product code:

Batch 84702; Batch 72766

Recalling firm:

Young Dental Manufacturing Co, LLC

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

Recall #:

84220

Lot/product code:

All Lots within Expiry: US Lot codes: 61650, 61657, 61779, 61780, 61825, 61883, 61884, 61906, 61911, 62578, 62608, 62703, 62812, 62874 and 62941 OUS Lot codes: 61566, 61580, 61626, 61642, 61685, 61846, 61847, 61955, 61966, 62008, 62301, 62053, 62066, 62108, 62130, 62263, 62297, 62318, 62380, 62538, 62636, 62678, 62683, 62719, 62745, 62749, 62769 and 62890

Recalling firm:

Allergan PLC

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

Recall #:

84191

Lot/product code:

Lot Numbers: 0009754921 0009921274 0009940846 0009921273 0009921276 0009952564

Recalling firm:

Medtronic Navigation, Inc.

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

Recall #:

84191

Lot/product code:

Lot Numbers: 66503918A 066513519A 066529218A 066535518A 66503919 066513519C 66531018 066512319A 066513519E 066531018A 066512319C 66529218 66535518

Recalling firm:

Medtronic Navigation, Inc.

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

Recall #:

85416

Lot/product code:

Serial numbers LR051A58B027, LR051A58B028, and LR051A58B029.

Recalling firm:

Shimadzu Medical Systems

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

Recall #:

84309

Lot/product code:

Serial Numbers: 10110770 11030805 11030806 11070845 11070848 11070849 11110900 12020978 12020982 12030999 12041003 12061014 12061018 12061020 12081040 12091074 12101104 12121186 12121187 13031215 13101263 14021301 14031313 14041321 14051332 14071353 14081359 14091368 14091371 14121400 14121403 15021426 15031440 15041444 15091473 15091478 15101484 15101487 15121505 16011512 16021514 16021517 16021518 16041533 16121595 19011923

Recalling firm:

Villa Sistemi Medicali S.P.A.