Recalls affecting Nebraska

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

Recall #:

88797

Lot/product code:

UDI 03573026156947, Lot #: 1008781470

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026444204, Lot #s: 1008686690

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026161637, Lot #: 1008757880

Recalling firm:

bioMerieux, Inc.

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

Recall #:

88797

Lot/product code:

UDI 03573026620738, Lot #: 1008710950

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 #:

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 #:

89023

Lot/product code:

ProxiDiagnost N90

Recalling firm:

Philips Healthcare

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 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 03573026263010, Lot #: 1008861590

Recalling firm:

bioMerieux, Inc.

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 03573026156930, Lot #: 1008848600

Recalling firm:

bioMerieux, Inc.

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 #:

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 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 03573026064532, Lot #: 1008890110

Recalling firm:

bioMerieux, Inc.

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 #:

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 #:

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 # 166300 / UDI: 10841307101796

Recalling firm:

Implant Direct Sybron Manufacturing LLC

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 #:

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 #:

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 #:

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