Recalls affecting Massachusetts

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

Recall #:

88746

Lot/product code:

Serial Numbers:  US: BS16904 BS16905 BS16906 BS16909 BS16910 BS16911 BS16912 BS16913 BS16914 BS16915 BS16916 BS16917 BS16918 BS16921 BS16923 BS16925 BS17930 BS17934 BS17935 BS17936 BS17937 BS18900 BS18901 BS18924 BS18931 BS18938 BS18939 BS18940 BS18942 BS18943 BS18945 BS18946 BS18947 BS18948 BS18949 BS18950 BS18951 BS18952 BS18953 BS18954 BS18955 BS18956 BS18957 BS18958 BS18959 BS18960 BS18961 BS18962 BS18963 BS18964 BS18965 BS18966 BS18967 BS18968 BS18969 BS18970 BS18971 BS18972 BS18973 BS18974 BS18975 BS18976 BS18977 BS18979 BS18980 BS18981 BS18982 BS18983 BS18984 BS18985 BS18986 BS18987 BS18988 BS18989 BS18990 BS18991 BS18992 BS18993 BS18994 BS18995 BS18996 BS18997 BS18998 BS18999 BS19037 BS19038 BS19039 BS19040 BS19041 BS19043 BS19047 BS19049 BS19050 BS19052 BS19053 BS19054 BS19057 BS19058 BS19059 BS19060 BS19061 BS19065 BS20066 BS20067 BS20072 BS20073 BS20079 BS20080 BS20086 BS20092 BS20100 BS20103 BS20107 BS21112 BS21115 BS21121 BS21129 BS21137 BS21138  OUS:  BS15902 BS15903 BS16007 BS16919 BS16928 BS16929 BS17008 BS17010 BS17013 BS17021 BS17022 BS17023 BS18024 BS18026 BS18027 BS18028 BS18030 BS18031 BS19032 BS19033 BS19034 BS19035 BS19036 BS19042 BS19051 BS19056 BS19062 BS19064 BS20068 BS20069 BS20070 BS20071 BS20074 BS20075 BS20076 BS20077 BS20078 BS20082 BS20084 BS20085 BS20090 BS20095 BS20098 BS20099 BS20102 BS20105 BS20106 BS21108 BS21109 BS21114 BS21124 BS21128 BS21132 BS21133 BS21134

Recalling firm:

MEDTECH SAS

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

Recall #:

89800

Lot/product code:

Product name (build number) UDI-DI RayStation 4.0 (4.0.0.14) to RayStation 5 Service Pack 2 (5.0.2.35) N/A RayStation 5 Service Pack 3 (5.0.3.17) 07350002010020 RayStation 6/RayPlan 2 (6.0.0.24) 07350002010013 RayStation 6/RayPlan 2 Service Pack 1 (6.1.1.2) 07350002010082 RayStation 6/RayPlan 2 Service Pack 2 (6.2.0.7) 07350002010075 RayStation 6/RayPlan 2 Service Pack 3 (6.3.0.6) 07350002010242 RayStation/RayPlan 7 (7.0.0.19) 07350002010068 RayStation/RayPlan 8A (8.0.0.61) 07350002010112 RayStation/RayPlan 8A Service Pack 1 (8.0.1.10) 07350002010136 RayStation/RayPlan 8B (8.1.0.47) 07350002010129 RayStation/RayPlan 8B Service Pack 1 (8.1.1.8) 07350002010204 RayStation/RayPlan 8B Service Pack 2 (8.1.2.5) 07350002010235 RayStation/RayPlan 9A (9.0.0.113) 07350002010174 RayStation/RayPlan 9B (9.1.0.933) 07350002010266 RayStation/RayPlan 9B Service Pack 1 (9.2.0.483) 07350002010297 RayStation/RayPlan 10A (10.0.0.1154) 07350002010303 RayStation/RayPlan 10A Service Pack 1 (10.0.1.52) 07350002010365 RayStation/RayPlan 10B (10.1.0.613) 07350002010310 RayStation 11A (11.0.0.951) 07350002010389 RayStation 11A Service Pack 1 (11.0.1.29) 07350002010433

Recalling firm:

RAYSEARCH LABORATORIES AB

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

Recall #:

89023

Lot/product code:

CombiDiagnost R90

Recalling firm:

Philips Healthcare

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

Recall #:

88797

Lot/product code:

UDI 03573026064525, Lot #: 1008769120

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026263010, Lot #: 1008861590

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026229146, Lot #s: 1008730880

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026620745, Lot #: 1008671430, 1008763910

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026156930, Lot #: 1008848600

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026064532, Lot #: 1008890110

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026064952, Lot #s: 1008685490, 1008766980, 1008775630, 1008873180, 1008911240

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026458270, Lot #: 1008714880, 1008824220

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026138585, Lot #: 1008694980, 1008700260, 1008828980

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026447151, Lot #: 1008636750, 1008768920, 1008857410

Recalling firm:

bioMerieux, Inc.

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

Recall #:

89023

Lot/product code:

ProxiDiagnost N90

Recalling firm:

Philips Healthcare

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

Recall #:

88761

Lot/product code:

Clinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081

Recalling firm:

Medtronic Neuromodulation

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

Recall #:

88859

Lot/product code:

lot # 166300 / UDI: 10841307101796

Recalling firm:

Implant Direct Sybron Manufacturing LLC

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

Recall #:

88825

Lot/product code:

Lot #/Expiration Date: 12175N/11.30.2021, 12722N/01.31.2022, X12122N/01.31.2022, X12724N/08.31.2022

Recalling firm:

DiaSorin Molecular LLC

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

Recall #:

88859

Lot/product code:

lot # 166297 / UDI: 10841307101789

Recalling firm:

Implant Direct Sybron Manufacturing LLC

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

Recall #:

88820

Lot/product code:

Artis zeego systems with Artis patient table and AppSW VD20C/VD20N

Recalling firm:

Siemens Medical Solutions USA, Inc

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

Recall #:

88718

Lot/product code:

Manufactured between January 19, 2017 and June 14, 2021 with the serial number range from M2005054 to 1231112011

Recalling firm:

TiSport, Llc

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

Recall #:

89020

Lot/product code:

Azurion 2.1(L1) and 2.1(L2)

Recalling firm:

Philips Healthcare

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

Recall #:

88846

Lot/product code:

All lots of the following sizes: a. XS, REF 47459, UDI (01)20680651474593 b. S, REF 47460, UDI (01)20680651474609 c. M, REF 47461, UDI (01)20680651474616 d. L, REF 47462, UDI (01)20680651474623 e. XL, REF 47463, UDI (01)20680651474630

Recalling firm:

O&M HALYARD INC

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

Recall #:

88792

Lot/product code:

All units

Recalling firm:

Siemens Healthcare Diagnostics, Inc

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

Recall #:

88792

Lot/product code:

All units.

Recalling firm:

Siemens Healthcare Diagnostics, Inc

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

Recall #:

D-0364-2022

Lot/product code:

Lot 2091A, exp 7/2023

Recalling firm:

Revive Personal Products Company