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. 2,484 recalls have been distributed to South Dakota in the last 12 months.
Showing 12441–12460 of 47,632 recalls
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mickey Mouse Hand Sanitizer Recalled by Best Brands Consumer Products, Inc....
The Issue: Chemical Contamination; FDA analysis found product to contain methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Mandalorian Hand Sanitizer Recalled by Best Brands Consumer Products,...
The Issue: Chemical Contamination; FDA analysis found product to contain benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink Pussycat SENSUAL ENHANCEMENT capsule Recalled by Pink Toyz Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use...
The Issue: Presence of Particulate Matter: Product was found to contain silica and iron...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Preferred Pharmaceuticals Recalled by Preferred Pharmaceuticals, Inc. Due to...
The Issue: Out of specification results observed in dissolution during long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MedMinder Medication Dispenser- Intended to serve as a medication reminder...
The Issue: Discontinuation of the Emergency Alert watch or pendant will no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...
The Issue: The nickel-sensitivity statement on the outer carton may be partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code:...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Uretero-reno videoscope Recalled by Olympus Corporation of the...
The Issue: The bending section of the URF-V2 may crack, resulting in an abnormal shape...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and...
The Issue: Products do not meet length and diameter specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Medtronic formerly...
The Issue: The audible alarm may not sound and/or the omni-directional LED visual alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution 1.5% w/w Recalled by Preferred...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit Recalled by Wilton...
The Issue: Milk is missing from the product's allergen Contains statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...
The Issue: QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.