Recalls affecting South Carolina

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 #:

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 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 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 03573026064525, Lot #: 1008769120

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 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 #:

89023

Lot/product code:

DigitalDiagnost C90

Recalling firm:

Philips Healthcare

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 #:

89109

Lot/product code:

All da Vinci SP Surgical systems with software version OS4 v4.0.0 (P4_B327)

Recalling firm:

Intuitive Surgical, Inc.

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 #:

89023

Lot/product code:

CombiDiagnost R90

Recalling firm:

Philips Healthcare

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 #:

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 #:

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

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

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

D-0256-2022

Lot/product code:

a) Lots: 152838, 152156, 152151, 151708, 151693, 151375, 151131, 151114, Exp: 7/31/2022, b) Lots: 152245, 151822, 151708, 151160, 151131, Exp: 7/31/2022, c) Lot #: 152614, Exp: 7/31/2022.

Recalling firm:

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

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

Recall #:

88792

Lot/product code:

All units

Recalling firm:

Siemens Healthcare Diagnostics, Inc