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. 2,512 recalls have been distributed to South Dakota in the last 12 months.
Showing 10041–10060 of 27,558 recalls
Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...
The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...
The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee Recalled by...
The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIROS D-Vial Prep Set Recalled by Sirtex Medical Limited Due to There is a...
The Issue: There is a potential presence of particulate matter in the D-Vial.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...
The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...
The Issue: The product may be contaminated with Burkholderia cepacia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...
The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...
The Issue: Teleflex is voluntarily recalling the products above due to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...
The Issue: Discoloration and turbidity were present in the specified lots of STMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...
The Issue: Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...
The Issue: The mirror may become detached and fall from the unit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.