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 9801–9820 of 47,632 recalls
Recalled Item: Clobetasol propionate Cream USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: Low assay result observed during long-term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SenSight Connector Plug Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is requesting return of a small number of units of the SenSight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of...
The Issue: Screw connection between the turbine head and the push button may loosen and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) Recalled by...
The Issue: Undeclared FD&C Yellow No. 5
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due...
The Issue: The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v Recalled by Urban...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v) Recalled by Urban Electric...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...
The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...
The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D...
The Issue: C-Arm unexpected movement may cause blunt trauma should the tube arm impinge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph mCT: a) Flow 64-4R Seismic Recalled by Siemens Medical...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Vision: a) 450 Recalled by Siemens Medical Solutions USA,...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by SUN...
The Issue: Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S2 Racepinephrine Inhalation Solution Recalled by Nephron Sc Inc Due to...
The Issue: Short Fill
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator (racephedrine...
The Issue: Short Fill
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allopurinol Tablets USP Recalled by Accord Healthcare, Inc. Due to Presence...
The Issue: Presence of Foreign Substance: Presence of a small piece of green plastic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Nephron Sc Inc Due to CGMP...
The Issue: CGMP Deviations: potential for trace amounts of product carryover.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Nephron Sc Inc Due to CGMP...
The Issue: CGMP Deviations: potential for trace amounts of product carryover.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fiber Powder Recalled by Ortho Molecular Products, Inc. Due to Raw material...
The Issue: Raw material tested positive for Cronobacter sakazakii.
Recommended Action: Do not consume. Return to store for a refund or discard.