Recalls affecting Iowa

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

Recall #:

D-0361-2020

Lot/product code:

Lot #: TCI , Exp 03/21

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0356-2020

Lot/product code:

Lot #: RGA 7/19 7/31/2017; RGE 7/19 8/11/2017; RGG7/19 8/11/2017; RGH 7/19 8/17/2017; RHM 8/19 9/14/2017; RJB 10/19 10/23/2017; RJA 10/19 10/23/2017; SCA 3/20 3/22/2018; SIC 9/20 10/9/2018; TAP 1/21 2/26/2019; TDE 4/21 5/30/2019

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0358-2020

Lot/product code:

Lot #: RJH, Exp 10/19; SCC, Exp 3/21; SGA, Exp 7/21; SGH, Exp 7/21; SHH, Exp 8/21; SLL, Exp 12/21; TAC, Exp 1/22

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0411-2020

Lot/product code:

18229 9/21 18031 1/21 17131 5/20 17059 3/20 17008 1/20 19056 03/22

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0485-2020

Lot/product code:

Lot #: 17008, Exp 01/20

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0398-2020

Lot/product code:

16250 09/19 16268 10/19 16301 11/19 17088 3/20 17109 4/20 17318 10/20 17323 10/20 18014 1/21 18045 2/21 18059 3/21 18063 3/21 18117 5/21 18134 5/21

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0462-2020

Lot/product code:

17210 7/19 17378 12/19 18175 7/20

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0392-2020

Lot/product code:

Lot #: 17251 8/19 17269 9/19 17360 12/19 18012 1/20 18106 4/20 18275 11/20 18275 11/20

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0426-2020

Lot/product code:

17112 4/20 17303 10/20 18032 2/21 18072 3/21 18193 8/20 18235 9/21 18285 11/21 19004 1/22 19102 4/22 16260 9/19

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0362-2020

Lot/product code:

Lot #: 19105, Exp 04/22; 19050, Exp 02/22

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0416-2020

Lot/product code:

SAP 1/20 3/16/2018 SFI 6/20 8/16/2018 SLA 12/20 1/4/2019 TBM 2/21

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0396-2020

Lot/product code:

18043 2/20 18115 5/20 18300 12/20 18300 12/20 18116 5/20 18115 5/20 18044 2/20 18043 2/20

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0352-2020

Lot/product code:

Lot #: RGC, Exp 7/19; RHB, RHC, Exp 8/19; RID, RIC, RIG, Exp 9/19; RKH, RKI, RKJ, RKK, RKL, Exp 11/19; RLM, Exp 12/19; SAI, Exp 1/20; SBG, SBH, Exp 2/20; SCF, Exp 3/20, SEA, Exp 5/20; SFA, SFB, Exp 6/20; SHA, Exp 8/20; SIB, Exp 9/20; SJC, Exp 10/20; TAB, TAF, Exp 1/21; TBP, TBQ, Exp 2/21; TCV, TCW, Exp 3/21

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0389-2020

Lot/product code:

Lot #: QHI 08/19 QJG 10/19 RBA 02/20 RCF 03/20 RCM 03/20 RDJ 04/20 RFA 06/20 RHI 08/20 RJI 10/20 RKG 11/20 SBF 2/21 SDD 04/21

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0409-2020

Lot/product code:

17291 9/19 17385 12/19 18118 5/20

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

D-0470-2020

Lot/product code:

RHP 8/19 RLD 12/19 SDE 4/20 SID 9/20

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

83273

Lot/product code:

all Monaco Radiation Treatment Planning units installed with software version 5.10 or 5.11

Recalling firm:

Elekta Inc

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

Recall #:

83438

Lot/product code:

Burstberry

Recalling firm:

Gk Photonics Inc

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

Recall #:

83438

Lot/product code:

Logolas Laser Projection Series

Recalling firm:

Gk Photonics Inc

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

Recall #:

83438

Lot/product code:

Spectrum Laser Projection Series

Recalling firm:

Gk Photonics Inc

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

Recall #:

83438

Lot/product code:

ClubMax Laser Projection Series

Recalling firm:

Gk Photonics Inc

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

Recall #:

83438

Lot/product code:

Atom Laser Projection Series

Recalling firm:

Gk Photonics Inc

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

Recall #:

83438

Lot/product code:

Maxim Laser Projection Series

Recalling firm:

Gk Photonics Inc

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

Recall #:

90588

Lot/product code:

UDI-DI: 00856893004065; Software Versions 5.1 or 5.2; Serial Numbers Between xx0001 and xx0160

Recalling firm:

Aggredyne, Inc.

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

Recall #:

92390

Lot/product code:

Catalog Numbers / Lot Numbers: 100801 / A29318R 100802 / A29318S 100803 / A29318T 100804 / A29318U 100805 / A29318V UDI Codes: Not provided/None

Recalling firm:

New Standard Device Inc