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. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 8981–9000 of 27,558 recalls
Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...
The Issue: Potential for a wire protrusion through the left heart vent catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...
The Issue: Potential for a wire protrusion through the left heart vent catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Action De Gala Recalled by Aesthetics Systems Usa Inc Due to Ultrasound gels...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use...
The Issue: The SARS-CoV-2 Process Control (Pellet) contains RNA transcripts that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate Recalled...
The Issue: Complaint of tubes clotting due to variation of anticoagulant and/or tubes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS-CoV-2 Process Control (Swab) - Product Usage: intended for use Recalled...
The Issue: The product indicated is contaminated with a plasmid DNA that contains the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641 Recalled by...
The Issue: The rear heater plate and cover assembly that contains the electrical wiring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...
The Issue: Battery system data issue with the ultrasound system can intermittently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...
The Issue: Battery system data issue with the ultrasound system can intermittently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scrip Ultrasound Gel Clear Recalled by Scrip Inc Due to Ultrasound gels and...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scrip Creme All Purpose Lotion Intended for use in acoustic Recalled by...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVENA PICC Sleeve Recalled by Queen Comfort Products lLC Due to Marketed...
The Issue: Marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed tomography x-ray systems with software syngo.CT VA20A_SP4a Recalled...
The Issue: Software versions may result in sporadic problems causing scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoLink Bone Graft Harvester Recalled by In2bones USA, LLC Due to Complaints...
The Issue: Complaints were received of CoLink Bone Graft Harvesters breaking at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.