Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,373 recalls have been distributed to South Dakota in the last 12 months.
Showing 23401–23420 of 27,558 recalls
Recalled Item: IRK QRG for the da Vinci Standard Surgical System Recalled by Intuitive...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vessel Sealer QRG for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Rubber Latex QRG for the da Vinci Standard Surgical System Recalled...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 8000 analyzer series Operators Manual Roche cobas Filter label:...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System...
The Issue: A portion of the BBL Crystal Enteric/Nonfermentor (E/NF) Identification kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche MODULAR ANALYTICS EVO Serum Work Area (SWA) Recalled by Roche...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is Recalled by Brainlab AG...
The Issue: Brainlab Navigation Software Spine & Trauma 3D 2.0/2.1 offers automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insert for IRK for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas 6000 analyzer series Operators Manual Roche cobas Recalled by Roche...
The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vessel Sealer Addendum for the da Vinci Standard Surgical System Recalled by...
The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VAGINAL PROCEDURE PACK CUSTOM ED CONTENTS: (1) DRAPE LITHOTOMY 110" Recalled...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory...
The Issue: The interface fails to send abnormal flags for Lab test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO PACK EXTREMITY CUSTOMED CONTENTS: (1) TABLE COVER REINFORCED 50"...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAP Abdom w/pouch Customed code 900-2619 Recalled by Customed, Inc Due to...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E..N.T. PACK - (5) SPONGE TONSIL 7/8 XRD (1) TABLE Recalled by Customed, Inc...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Customed, Inc Due to Customed has determined...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPY COLORECTAL SURGICAL PACK code 900-2259A Recalled by Customed,...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPY PACK- - (1) DRAPE LAP ABDOMINAL WITH POUCH (1) Recalled by...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY PACK I (1) CUSTOMED CONTENTS: (1) TOWELS ABSORBENT 15" Recalled...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC LAP PACK - ( I) SHEET MINOR LAP 102" Recalled by Customed, Inc Due...
The Issue: Customed has determined that there is the possibility that packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.