State
73,597 recalls have nationwide distribution and so reach South Dakota. 2,686 additional recalls listed South Dakota specifically in their distribution scope.
Of the 2,686 recalls naming South Dakota we have scored against our rubric, 399 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 749 (28%) are Severe.
Which agencies issued them
These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blue Apron is recalling meal kits delivered the week of July 27, 2020, because the onions included may be contaminated with Salmonella.
Caravan Global is recalling about 2,700 Sports Armed/Padded Arm Bagged Chairs sold at H-E-B stores in Texas due to a defect that can cause the seat to rip from the frame.
Life Technologies is recalling the TaqPath RT-PCR COVID-19 Kit due to software issues that may cause invalid, inconclusive, or false test results.
Motor Coach Industries is recalling 2019 D45 CRT LE coaches because seat belt retractors in the last row may not function, increasing injury risk in collisions.
Pedego is recalling about 11,600 electric bikes because an improperly manufactured electrical cable can cause unexpected acceleration, posing a fall hazard.
Braxton Creek RV is recalling 2020 Bushwhacker and Bushwhacker Plus travel trailers because tire stickers list 65 PSI instead of the correct 50 PSI maximum.
Terumo is recalling two Ultrasonic Air Sensors because a manufacturing defect may cause intermittent connections and false air bubble alarms during extracorporeal procedures.
Life Technologies is recalling the TaqPath RT-PCR COVID-19 Kit due to software issues that may cause invalid, inconclusive, or false test results.
Imactis is recalling Patient Fiducial components because they may separate from the body, potentially causing navigation inaccuracies or improper needle trajectory.
Longhorn Vaccines and Diagnostic is recalling PrimeStore Molecular Transport Medium tubes because the solution may produce cyanide gas when exposed to bleach.
Ford is recalling 620,246 2020 vehicles because a poor electrical connection may cause the rearview camera to display a blank or distorted image, increasing crash risk.
Integra LifeSciences is recalling 2 units of the Padgett Electric Dermatome Set because the handpiece cable melts after sterilization.
Randox Laboratories is recalling Lactate Dehydrogenase P-L reagent to address reagent carryover issues on RX instruments that may cause erroneous test results.
RLC Labs Inc. is recalling Nature-Throid tablets due to Current Good Manufacturing Practice (CGMP) deviations. The product was manufactured under conditions found to be subpotent.
Roche Diagnostics is recalling 11,870 Elecsys Anti-TPO Assay kits because internal studies found the radio frequency interference claim no longer met for specific cobas e analyzers.
RLC Labs Inc. is recalling Nature-Throid tablets due to manufacturing deviations. The products were manufactured under conditions found to be subpotent.
Tosoh Bioscience is recalling five lots of AIA-PACK HCG Calibrator Sets because decreased stability may cause measured HCG concentrations to be up to 20% lower than actual.
Boston Scientific is recalling 40 units of WallFlex Biliary RX stents that were mislabeled as fully covered devices. The error involves the 10mm x 60mm size.
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions associated with subpotent products.
Terumo is recalling 100 Ultrasonic Air Sensors because a manufacturing defect may cause false air bubble alarms during extracorporeal procedures.
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions found to be subpotent.
Tosoh Bioscience is recalling 39 boxes of AIA-PACK BHCG Calibration Sets due to decreased stability that may cause inaccurate HCG concentration measurements.
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions associated with subpotency. The recall covers all lots with expiry dates between October 2020 and July 2023.
RLC Labs Inc. is recalling WP Thyroid tablets because they were manufactured under conditions associated with subpotent products.
RLC Labs Inc. is recalling Nature-Throid tablets because they were manufactured under conditions found to be subpotent.