Recalls affecting Colorado

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

Recall #:

D-0450-2020

Lot/product code:

17209 7/21 18168 7/22 18217 8/22 18260 10/22 19094 4/23

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-0445-2020

Lot/product code:

17236 8/19 17334 11/19 18015 1/20

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-0385-2020

Lot/product code:

Lot #: SAS 1/21 SIA 9/21 SFE 6/21 SAS 1/21 SFE 6/21 SIA 9/21 RIE 9/20 REH 5/20 RAD 1/20 TAH 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-0451-2020

Lot/product code:

17208 7/21 17209 7/21 19001 1/23

Recalling firm:

Altaire Pharmaceuticals, Inc.

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

Recall #:

83409

Lot/product code:

Software 5.0.3 Serial Numbers: 5786 13184 30000 34450 34886 35214 35455 35510 5943 13195 34023 34457 34887 35222 35456 35514 6037 13275 34040 34464 34891 35224 35457 35519 6263 13486 34045 34468 34892 35226 35458 35522 6325 13592 34068 34473 34893 35231 35459 35524 6529 13635 34907 34477 34894 35241 35460 35525 6531 13640 34080 34495 34896 35245 35462 35526 6828 13648 34081 34496 34897 35259 35463 35529 7188 13654 34083 34504 34901 35265 35464 35530 7232 13755 34086 34507 34902 35278 35465 35532 7295 13773 34112 34525 34701 35279 35466 35537 7297 13777 34116 34555 34914 35287 35467 35538 7340 13797 34123 34557 34923 35312 35468 35542 7349 13813 34124 34562 34931 35322 35469 35544 7409 13841 34129 34567 34951 35335 35471 35545 7432 13858 34143 34571 34977 35338 35472 35547 7480 13862 34152 34580 34981 35344 35473 35548 7725 13874 34153 34582 34986 35352 35474 35549 7973 13886 34161 34588 34988 35360 35475 35550 8049 13904 34181 34589 34366 34076 35476 35557 8052 13948 34184 34596 35001 35381 35477 35558 10109 14021 34192 34597 35011 35382 35478 35559 10198 14108 34204 34603 35013 35384 35479 35560 10389 14153 34221 34610 35014 35386 35497 35561 10630 14178 34229 34622 35015 35387 35481 35564 11177 14207 34237 34628 35024 35398 35482 35565 11392 14209 34245 34631 35030 35399 35483 35566 11417 14219 34247 34637 35033 35406 35484 35567 11431 14262 34252 34644 35042 35408 35485 35568 11590 14356 34265 34646 35045 35411 35486 35569 11609 14564 34268 34649 35061 35412 35487 35570 11938 14617 34269 34666 35070 35435 35488 35571 12010 14629 34281 34695 35075 35436 35489 35572 12052 14676 34297 34396 35079 35438 35490 35573 12053 14678 34322 34719 35083 35439 35491 35574 12106 14689 34338 34727 35086 35440 35492 35575 12175 14697 34342 34732 35094 35441 35493 35576 12203 14698 34343 34757 35097 35442 35495 35577 12275 14706 34349 34765 35115 35443 35496 47000 12304 14748 35362 34771 35118 35444 35480 12308 14764 34373 34787 35129 35445 35498 12435 14840 34392 34802 35132 35446 35499 12658 14856 35451 34813 35141 35447 35500 12758 14907 34401 34824 35179 35448 35501 12924 14941 34403 34825 35180 35449 35502 12979 14946 34410 34847 35182 35450 35503 13022 15028 34413 34856 35188 35000 35504 13135 15129 34421 34863 35202 35452 35505 13173 15226 34426 34880 35209 35453 35507 13183 15298 34447 34884 35213 35454 35508

Recalling firm:

Qiagen Sciences LLC

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

Recall #:

D-0420-2020

Lot/product code:

18164 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-0453-2020

Lot/product code:

Lot #: 18008 1/20 19105 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-0397-2020

Lot/product code:

16260 9/19 17303 10/20 18032 2/21 18235 9/21 18285 11/21 19021 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-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-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-0402-2020

Lot/product code:

19087 3/21 17289 9/19 19087 03/21 18122 5/20

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:

Maxim 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 #:

83465

Lot/product code:

batches V14.V976 and V14.W107

Recalling firm:

Owen Mumford USA, Inc.

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

Recall #:

83465

Lot/product code:

Lot/Unit Number: V14

Recalling firm:

Owen Mumford USA, 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

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 #:

83500

Lot/product code:

All Lots: Note:This product was not distributed within the US

Recalling firm:

Allergan PLC

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

Recall #:

83500

Lot/product code:

All Lots: Note:This product was not distributed within the US

Recalling firm:

Allergan PLC

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

Recall #:

83500

Lot/product code:

All Lots: Note:This product was not distributed within the US

Recalling firm:

Allergan PLC