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. 2,467 recalls have been distributed to South Dakota in the last 12 months.
Showing 14461–14480 of 27,558 recalls
Recalled Item: EDS Light Suspension Recalled by Stryker Communications Due to There is a...
The Issue: There is a potential the joint in the suspension of the device is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux,...
The Issue: The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for...
The Issue: Insufficient seal on the sterile barrier of the device, compromising the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion Pack Recalled by LivaNova USA Due to 4-way stopcocks and stopcock...
The Issue: 4-way stopcocks and stopcock manifold assembled in certain perfusion tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled...
The Issue: Unintentional U-Arm movement
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips...
The Issue: kV/mA lockin not functioning as specified which may result in the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Volcano FFR software used in the following systems connected...
The Issue: Interoperability issue that affects certain systems that use the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Binding Site Human IgM Kit (for SPAPLUS) Recalled by The Binding Site Group,...
The Issue: Firm is offering advice to customers experiencing challenges when validating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 300 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 100 table Recalled by Deerfield Imaging, Inc. Due to Table may...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT 200 Recalled by Deerfield Imaging, Inc. Due to Table may drift in...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 3000 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated...
The Issue: Cosmetic imperfections on the surface of some lenses.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR Capillary High Flux Dialyzer Single Use Only Recalled by...
The Issue: Potential for external blood leaks from the dialyzer header
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 700 Thyroid Uptake System Recalled by Capintec Inc Due to There is a...
The Issue: There is a potential for the spring arm failure as a result of a broken...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...
The Issue: The firm has detected a potential risk using the command. After releasing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product...
The Issue: There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Coupler Forceps Recalled by Baxter Healthcare Corporation Due to...
The Issue: Potential presence of rust on Coupler Forceps (GEM4183C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.