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. 2,538 recalls have been distributed to South Dakota in the last 12 months.
Showing 4221–4240 of 27,558 recalls
Recalled Item: Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative...
The Issue: Foam gasket on the Evidence MultiSTAT chip heater assembly may not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime A3 C17/5 -A zirconium oxide Recalled by...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime C2 C17/5- A zirconium oxide Recalled by...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime BL1 C17/3- A zirconium oxide Recalled by...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime A2 C17/5 -A zirconium oxide Recalled by...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime B1 C17/5 -A zirconium oxide Recalled by...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPS e.max ZirCAD CER/in. Prime A1 C17/5 - A zirconium Recalled by IVOCLAR...
The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliSpace Cardiovascular software Recalled by Philips Medical...
The Issue: Study data is not able to be archived, copied, or exported with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8000-021-002 Recalled by Stryker Leibinger GmbH & Co. KG Due to Unreleased...
The Issue: Unreleased software was installed on customer systems resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Test Strips for Blood Recalled by Macherey Nagel Gmbh & Co. Kg Due...
The Issue: The reason for the recall is one of the test pads, for the parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaClear Lens Sheath. The InstaClear lens cleaner system and versatile...
The Issue: Potential for distal end of the sheath to break off during a procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Distal Access Catheter is a single-lumen Recalled by Stryker...
The Issue: Stryker Neurovascular is recalling their DAC- Distal Access Catheter -038...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Dako CoverStainer Recalled by Agilent Technologies Due to There...
The Issue: There is the potential for the front plexiglass door of the automated slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage Recalled by Andover...
The Issue: A packaging seal gap could impact the sterility of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Humidifier Recalled by Fisher & Paykel Healthcare, Ltd. Due to...
The Issue: Humidifier devices, used to deliver high flow respiratory therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124...
The Issue: Device may experience an interruption or loss of therapy in case of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASER Application Instrument Recalled by Karl Storz Endoscopy Due to Laser...
The Issue: Laser surgical instruments have no specific evidence of a validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version:...
The Issue: Due to unsupported 10 year expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oncology Essentials Package of the Spectral CT imaging system. Recalled...
The Issue: Potential for third party oncology marking laser to be off the gantry cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.