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. 2,295 recalls have been distributed to South Dakota in the last 12 months.
Showing 41061–41080 of 47,632 recalls
Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...
The Issue: There is the potential for the door roller assembly on the Plum LifeCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...
The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....
The Issue: Carestream received problem reports relating to apparent early failure of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...
The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...
The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marshmallow in the following flavors: chocolate Recalled by Araya, Inc Due...
The Issue: Product may contain undeclared allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Gift Boxes: SC 6 Oreos Recalled by Araya, Inc Due to Undeclared...
The Issue: Product may contain undeclared allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dry fruits covered in chocolate in the following flavors: orange peel...
The Issue: Product may contain undeclared allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate S'mores Araya Artisan Chocolate: 1545 W Grand Parkway S Recalled...
The Issue: Product may contain undeclared allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gourmet Bar in the following flavors: bacon Recalled by Araya, Inc Due to...
The Issue: Product may contain undeclared allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...
The Issue: The firm was notified by a customer of a cracked spring in the handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Subpotent; 18 month time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...
The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...
The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...
The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless...
The Issue: GE Healthcare has recently become aware of a software issue associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimper Model 9100CR26 The Crimper is indicated for use in Recalled by...
The Issue: Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Microbiology - Calculator/data processing module Recalled by...
The Issue: Potential for patient results being removed from LAB/EMR.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.