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. 1,663 recalls have been distributed to South Dakota in the last 12 months.
Showing 44081–44100 of 47,632 recalls
Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...
The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...
The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Sync C100-Physio Radiotransparent Defibrillation Electrodes Monophasic...
The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vermed Recalled by Heart Sync, Inc Due to On 4/18/13 HEARTSYNC became aware...
The Issue: On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...
The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...
The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Discoloration: This recall is being carried out due to a yellow to brown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orville Redenbacher's Classic Kettle Korn Recalled by Conagra Inc Due to...
The Issue: The kettle korn flavored ready-to-eat popcorn product may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...
The Issue: Philips has received one report from the field that there was an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoroscan Mini C-arm InSight2 Recalled by Hologic, Inc. Due to The audible...
The Issue: The audible alarm to alert the operator when cumulative irradiation time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...
The Issue: The audible alarm to alert the operator when cumulative irradiation time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...
The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer:...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...
The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...
The Issue: A complaint was received in which a hospital physicist indicated the dosage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...
The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...
The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.