Recalls affecting District of Columbia

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

Recall #:

86462

Lot/product code:

Batch Number: 2030895

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86450

Lot/product code:

Model Number: 940-02-54G Lot Number: 801Z1036

Recalling firm:

Encore Medical, LP

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

Recall #:

86420

Lot/product code:

CATALOG NUMBERS TGM212110X* TGM212115X* TGM212120X* TGM262610X* TGM262615X* TGM262620X* TGM282810X* TGM282815X* TGM282820X* TGM313110X* TGM313115X* TGM313120X* TGM343410X* TGM343415X* TGM343420X* TGM373710X* TGM373715X* TGM373720X* TGM404010X* TGM404015X* TGM404020X* TGM454510X* TGM454515X* TGM454520X* TGM262110X* TGM312610X* TGMR313110X* TGMR313115X* TGMR313120X* TGMR312610X* TGMR373710X* TGMR373715X* TGMR373720X* TGMR404010X* TGMR404015X* TGMR404020X* *X is a placeholder for enumeration code: E=EMEA, Australia, New Zealand; J=Japan  All lot numbers

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

86421

Lot/product code:

CATALOG NUMBERS TGM212110X* TGM212115X* TGM212120X* TGM262610X* TGM262615X* TGM262620X* TGM282810X* TGM282815X* TGM282820X* TGM313110X* TGM313115X* TGM313120X* TGM343410X* TGM343415X* TGM343420X* TGM373710X* TGM373715X* TGM373720X* TGM404010X* TGM404015X* TGM404020X* TGM454510X* TGM454515X* TGM454520X* TGM262110X* TGM312610X* TGMR313110X* TGMR313115X* TGMR313120X* TGMR312610X* TGMR373710X* TGMR373715X* TGMR373720X* TGMR404010X* TGMR404015X* TGMR404020X* *X is a placeholder for enumeration code: E=EMEA, Australia, New Zealand; J=Japan  All Lot Numbers

Recalling firm:

W L Gore & Associates, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2014002 2016196 2017814 2020051 2021388 2023272 2024724 2026266 2024759 2025289 2027469 2030955 2031023 2033400 2035501 2036291 2038328 2039263 2048404 2049924 2051020 2053921 2056432 2057402

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2013918 2016156 2017774 2018804 2021456 2023227 2024815 2025049 2027438 2029400 2029401 2033291 2033290 2034431 2034432 2034499 2034500 2034501 2034502 2035698 2037194 2039456 2045894 2048429 2048430 2051045 2051046 2049950 2049951 2053927 2056086 2056434

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2013151 2013152 2013903 2016145 2017808 2018788 2019884 2019885 2025277 2027457 2031003 2031002 2031054 2031055 2033509 2033508 2034401 2038771 2042570 2042752 2048296 2049809 2050955 2053788 2056330 2056872

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2042787

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2024948, 2024949, 2027356,2029176, 2044635

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2012719 2024702 2027393 2029380

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2025072

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2012718

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2012914, 2033371

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2012767 2013997 2016120 2017772 2018792 2019839 2021494 2022257 2024709 2025285 2027451 2027481 2030907 2030908 2031041 2033235 2033236 2034376 2034377 2034378 2035450 2036270 2049647 2049648 2053756 2049649 2050880 2050881 2056052 2056053

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2025354 2031116 2040066 2040702 2042557 2049638 2053749 2055239

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

86462

Lot/product code:

Batch Numbers: 2029229 2034457 2040701 2050876

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

90113

Lot/product code:

Dexcom G5 - All Serial Numbers; Basal-IQ Technology - Software Versions 6.3.01 and Earlier

Recalling firm:

Tandem Diabetes Care Inc

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

Recall #:

86419

Lot/product code:

Model 1600517 / Catalog number 1600517-001 Serial Numbers: 18F0017 18F0030 18G0003 18G0018 18G0019 18G0020 18G0021 18G0025 18H0016 18H0017 18H0018 18H0019 18H0026 18H0027 18I0003 18I0004 18I0005 18I0006 18I0018 18I0022 18I0023 18I0024 18I0025 18I0026 18I0027 18I0028 18I0029 18I0030 18J0001 18J0002 18J0003 18J0004 18J0005 18J0009 18J0010 18J0011 18J0012 18J0013 18J0014 18J0015 18J0016 18J0017 18J0018 18J0019 18J0020 18J0021 18J0022 18J0023 18J0024 18J0025 18J0026 18J0037 18J0038 18J0039 18J0040 18J0041 18L0012 18L0014 18L0017 18L0018 18L0019 18L0020 18L0021 18L0023 19B0021 19B0022 19B0023 19B0024 19B0025 19B0028 19B0029 19B0030 19B0038 19B0041 19B0042 19B0043 19B0044 19B0051 19B0052 19B0053 19B0054 19B0055 19B0056 19B0058 19B0059 19E0004 19E0005 19E0008 19E0009 19E0011 19E0012 19E0013 19E0014 19E0015 19E0016 19E0017 19E0028 19E0029 19E0030 19E0035 19E0037 19E0047 19E0048 19E0053 19E0054 19E0055 19E0056 19E0057 19E0058 19E0060 19E0063 19E0064 19E0068 19E0069 16A0015 16A0016 16G0024 16I0007 16I0026 16I0027 16I0028 16I0029 16K0027 17A0009 17B0008 17B0009 17B0010 17B0011 17B0012 17B0013 17B0039 17B0040 17B0041 17B0049 17B0050 17C0012 17C0013 17E0033 17G0004 17G0024 17G0025 19E0006 19E0007 19E0010

Recalling firm:

Bien-Air Surgery Sa

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

Recall #:

86419

Lot/product code:

Model 1600983 / Catalog number 1600983-001 Serial Numbers: 16D0002 16D0003 16D0004 16D0005 16D0006 16D0007 16D0008 16D0009 16D0010 16D0011 16D0012 16D0013 16D0014 16D0015 16D0016 16D0017 16D0018 16D0019 16D0020 16D0021 16D0022 16D0023 16D0024 16D0025 16D0026 16D0027 16D0028 16D0029 16D0030 16D0031 16D0032 16D0033 16D0034 16D0035 16D0036 16D0037 16D0038 16D0039 16D0040 16D0041 16D0042 16D0043 16D0044 16D0045 16D0046 16D0047 16D0048 16D0049 16D0050 16D0051 16E0001 16E0002 16E0003 16E0004 16E0005 16E0006 16E0007 16E0008 16E0009 16E0010 16E0011 16E0012 16E0013 16E0014 16E0015 16E0016 16E0017 16E0018 16E0019 16E0020 16E0021 16E0022 16E0023 16E0024 16E0025 16E0026 16E0027 16E0028 16E0029 16E0030 16E0031 16E0032 16E0033 16E0034 16E0035 16E0036 16E0037 16E0038 16E0039 16E0040 16E0041 16E0042 16E0043 16E0044 16E0045 16E0046 16E0047 16E0048 16E0049 16E0050 16F0001 16F0002 16F0003 16F0004 16F0005 16F0006 16F0007 16F0008 16F0009 16F0010 16F0011 16F0012 16F0013 16F0014 16F0015 16F0016 16F0017 16F0018 16F0019 16F0020 16F0021 16F0022 16F0023 16F0024 16F0025 16F0026 16F0027 16F0028 16F0029 16F0030 16H0001 16H0002 16H0003 16H0004 16H0005 16H0006 16H0007 16H0008 16H0009 16H0010 16H0011 16H0012 16H0013 16H0014 16H0015 16H0016 16H0017 16H0018 16H0019 16H0020 16H0021 16H0022 16H0023 16H0024 16H0025 16H0026 16H0027 16H0028 16H0029 16H0030 16I0001 16I0002 16I0003 16I0004 16I0005 16I0006 16I0007 16I0008 16I0009 16I0010 16I0011 16I0012 16I0013 16I0014 16I0015 16I0016 16I0017 16I0018 16I0019 16I0020 16I0021 16I0022 16I0023 16I0024 16I0025 16I0026 16I0027 16I0028 16I0029 16I0030 16I0031 16I0032 16I0033 16I0034 16I0035 16I0036 16I0037 16I0038 16I0039 16I0040 16J0001 16J0002 16J0003 16J0004 16J0005 16J0006 16J0007 16J0008 16J0009 16J0010 16J0011 16J0012 16J0013 16J0014 16J0015 16J0016 16J0017 16J0018 16J0019 16J0020 16J0021 16J0022 16J0023 16J0024 16J0025 16J0026 16J0027 16J0028 16J0029 16J0030 16K0001 16K0002 16K0003 16K0004 16K0005 16K0006 16K0007 16K0008 16K0009 16K0010 16K0011 16K0012 16K0013 16K0014 16K0015 16K0016 16K0017 16K0018 16K0019 16K0020 16K0021 16K0022 16K0023 16K0024 16K0025 16K0026 16K0027 16K0028 16K0029 16K0030 17D0001 17D0002 17D0003 17D0004 17D0005 17D0006 17D0007 17D0008 17D0009 17D0010 17D0011 17D0012 17D0013 17D0014 17D0015 17D0016 17D0017 17D0018 17D0019 17D0020 17D0021 17D0022 17D0023 17D0024 17D0025 17D0026 17D0027 17D0028 17D0029 17D0030 17D0031 17D0032 17D0033 17D0034 17D0035 17D0036 17D0037 17D0038 17D0039 17D0040 17D0041 17D0042 17F0001 17F0002 17F0003 17F0004 17F0005 17F0006 17F0007 17F0008 17F0009 17F0010 17F0011 17F0012 17F0013 17F0014 17F0015 17F0016 17F0017 17F0018 17F0019 17F0020 17F0021 17F0022 17F0023 17F0024 17F0025 17F0026 17F0027 17F0028 17F0029 17F0030 17F0031 17F0032 17F0033 17F0034 17F0035 17F0036 17F0037 17F0038 17F0039 17F0040 17F0041 17F0042 17F0043 17F0044 17F0045 17F0046 17F0047 17F0048 17F0049 17F0050 17F0051 17F0052 17F0053 17F0054 17F0055 17F0056 17F0057 17F0058 17F0059 17F0060 17F0061 17F0062 17F0063 17F0064 17F0065 17F0066 17F0067 18A0001 18A0002 18A0003 18A0004 18A0005 18A0006 18A0007 18A0008 18A0009 18A0010 18A0011 18A0012 18A0013 18A0014 18A0015 18A0016 18A0017 18A0018 18A0019 18A0020 18A0021 18A0022 18A0023 18A0024 18A0025 18A0026 18A0027 18A0028 18A0029 18A0030 18D0001 18D0002 18D0003 18D0004 18D0005 18D0006 18D0007 18D0008 18D0009 18D0010 18D0011 18D0012 18D0013 18D0014 18D0015 18D0016 18D0017 18D0018 18D0019 18D0020 18D0021 18D0022 18D0023 18D0024

Recalling firm:

Bien-Air Surgery Sa

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

Recall #:

86419

Lot/product code:

Model 1600686 / Catalog number 1600686-001 Serial Numbers: 18D0006 18D0007 18D0008 18D0009 18D0010 18D0013 18D0014 18D0015 18D0016 18D0017 18D0018 18D0019 18D0020 18D0021 18D0022 18D0023 18D0024 18D0025 18D0026 18D0027 18D0028 18D0029 18D0030 16A0005 16A0009 16A0010 16A0011 16A0014 17D0011 17G0006

Recalling firm:

Bien-Air Surgery Sa

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

Recall #:

D-0041-2021

Lot/product code:

Lot #s: 36748, 36818, 36697, Exp. 10/15/21 and 11/8/21

Recalling firm:

Genesis Partnership Company SA

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

Recall #:

D-0038-2021

Lot/product code:

Lot #: 37009, Exp. 02/10/2021

Recalling firm:

Genesis Partnership Company SA

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

Recall #:

D-0037-2021

Lot/product code:

Lot #: 072120, Exp. 01/21/2022

Recalling firm:

Genesis Partnership Company SA

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

Recall #:

86419

Lot/product code:

Model 1600407 / Catalog number 1600407-001 Serial Numbers: 16C0017 16F0013 16I0009 16K0017 17F0039 17I0015 17L0013

Recalling firm:

Bien-Air Surgery Sa

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

Recall #:

86532

Lot/product code:

Software Versions 5.1, 5.2, 5.3, 5.4, 5.5, and 5.7.

Recalling firm:

Fujifilm Medical Systems U.S.A., Inc.