Recalls affecting Vermont

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.

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-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-0536-2020

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-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-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-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-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-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-0537-2020

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-0541-2020

Lot/product code:

all lots

Recalling firm:

Sanofi-Aventis U.S. LLC

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

Recall #:

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: 0009665221 0009709452 0009960538

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 #:

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 #:

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 #:

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.

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

Recall #:

84309

Lot/product code:

Serial Numbers: 13101261

Recalling firm:

Villa Sistemi Medicali S.P.A.

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

Recall #:

84309

Lot/product code:

Serial Numbers: 08090531 09090591 10040680 15051450 11020798 17011602 17041639

Recalling firm:

Villa Sistemi Medicali S.P.A.

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: 08020473 11100873 15041446

Recalling firm:

Villa Sistemi Medicali S.P.A.

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

Recall #:

D-0528-2020

Lot/product code:

RA3018001-A Jul 2020 RA3018002-A Jul-2020 RA3018003-A Jul 2020 RA3018004-A Aug 2020 RA3018005-A Aug 2020 RA3018006-A Aug 2020 RA3018007-A Sep 2020 RA3018008-A Sep 2020 RA3018009-A Sep 2020 RA3018010-A Oct 2020 RA3019001-A Jan 2021 RA3019002-A Jan 2021 RA3019003-A May 2021

Recalling firm:

AuroMedics Pharma LLC