Recalls affecting New Jersey

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

Recall #:

D-0455-2020

Lot/product code:

17041 2/20 17186 6/20 18068 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-0357-2020

Lot/product code:

Lot #: RJD, Exp 10/19; SHG, Exp 8/20

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-0384-2020

Lot/product code:

Lot #: RJK 10/19 SBJ 2/20 SFG 6/20 SHI 8/20 SLB 12/20 TCM 03/21 TDC 4/21

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-0366-2020

Lot/product code:

Lot #: 17384, Exp 12/19; 17259, Exp 08/19; 19002, Exp 01/21; 19041, Exp 02/21; 18222, Exp 09/20; 18084, Exp 04/20

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-0412-2020

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-0395-2020

Lot/product code:

Lot #: QHE, Exp 08/19; QJD, Exp 10/19

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-0375-2020

Lot/product code:

Lot #: 17222 07/19 17386 12/19 19018 01/21 18016 01/20 18181 07/20 18104 04/20 19018 1/21

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-0457-2020

Lot/product code:

16250 09/19 17088 03/20 17307 10/20 17323 10/20 18014 1/21 18228 9/21 18261 10/21 19119 4/22

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-0390-2020

Lot/product code:

Lot #: QHF 08/19 QHI 08/19 QLA 12/19 RBA 02/20 RCF 03/20 RCM 03/20 RDJ 04/20 RFA 06/20 RHI 08/20 RJI 10/20 RKG 11/20 RLE 12/20 SAW 01/21 SBF 02/21

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-0439-2020

Lot/product code:

SFE 06/21

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-0374-2020

Lot/product code:

Lot #: 17196 08/19 17192 09/19 17355 11/19 18024 01/20 18036 02/20 18237 09/20 18293 12/20 18105 04/20 18179 07/20 19040 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-0438-2020

Lot/product code:

18099 4/20

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-0447-2020

Lot/product code:

18026 1/21 18100 4/21 19052 2/22 19130 5/22

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-0444-2020

Lot/product code:

Lot #: 17198, Exp 7/19; 17199, Exp 7/19; 17233, Exp 8/19; 17337, Exp 11/19; 17338, Exp 11/19; 18248, Exp 10/20

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-0413-2020

Lot/product code:

QHE 08/19 QJD 10/19

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-0487-2020

Lot/product code:

Lot #: 16195, Exp 7/19; 16211, Exp 8/19; 16216, Exp 8/19

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-0404-2020

Lot/product code:

17285 09/19 18067 03/20 18205 08/20 18067 3/20

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-0449-2020

Lot/product code:

17255 8/20 17362 12/20 18089 4/21 18138 6/21 6/22/2018 18146 6/21 18210 8/21 18211 8/21 18272 11/21 18273 11/21 18276 11/21 16283 10/31/2019

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-0454-2020

Lot/product code:

Lot #: 19087 03/21 18122 5/20 17289 9/19

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:

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:

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:

Burstberry

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