State
73,218 recalls have nationwide distribution and so reach South Dakota. 2,684 additional recalls listed South Dakota specifically in their distribution scope.
Of the 2,684 recalls naming South Dakota we have scored against our rubric, 401 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 567 (21%) are Severe.
Which agencies issued them
These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Coloplast is recalling 15 units of the Titan Touch Infr Zero Ang inflatable penile prosthesis (Lot Numbers 8849582, 8849603, 8904185) worldwide due to decreased wall thickness that may cause premature pump failure.
Coloplast Manufacturing is recalling the Titan 0-Deg Scrotal 18 Cm inflatable penile prosthesis (25 units) due to decreased wall thickness that may cause premature pump failure. Patients with affected lot numbers should contact their healthcare provider.
Sun Pharmaceutical is recalling Norepinephrine Bitartrate Injection due to a chemical impurity exceeding specification limits detected during routine monitoring. The recall affects 16,450 vials distributed nationwide.
Agilent Technologies is recalling 560 sample collection kits that were distributed with instructions for use the FDA had not approved.
TIPPCON LLC is recalling Perrona Hot Sauce Original with Chiltepin Peppers due to mold growth on the outside of the bottle. The affected product was distributed nationwide.
Pine Pharmaceuticals is recalling 932 syringes of Bevacizumab 2.5 mg/0.1 mL due to incorrect lot number labeling on the primary packaging. The affected lot (#66377, expiration 06/28/2023) was distributed nationwide.
Angiodynamics recalls NanoKnife 5-Probe Procedure Packs due to a programming error affecting RFID function. The probes may not be recognized by the NanoKnife generator, potentially delaying surgical procedures.
Coloplast Manufacturing recalls 20 units of Titan 0-Deg Scrotal inflatable penile prosthesis (Lot Numbers 8849601, 8849600, 8849621) with worldwide distribution. The specific reason for the recall is not specified in FDA records.
Pfizer recalls 1,926 bottles of MEKTOVI (binimetinib) due to incorrect expiration dates on labels. Bottles labeled March 2026 actually expire February 2025.
Hetero USA Inc. is recalling 2,352 bottles of Pantoprazole Sodium 40mg tablets due to manufacturing deviations that caused discoloration. The affected lot (PAN22542, exp. 9/2024) was distributed nationwide.
TIPPCON LLC is recalling Perrona Hot Sauce Black with Chiltepin Peppers due to mold growth detected on the outside of the bottle. No illnesses have been reported.
Focus Health Group is recalling 246 kits of Epinephrine Professional nationwide due to an incorrect NDC number printed on the outer carton. The labeling error does not affect the drug's safety or effectiveness.
TIPPCON LLC is recalling Perrona Hot Sauce Green with Chiltepin Peppers due to mold growth on the outside of the bottle. Approximately 8,230 cases were distributed nationwide.
Blue Bird is recalling 419 electric school buses because the anti-rollback feature may cause the vehicle to reverse faster than expected, increasing crash risk.
Nova Bus is recalling 2012-2014 LFS transit buses because emergency exit windows may be improperly installed or insufficient, potentially delaying evacuation.
Airstream is recalling 2023 Rangeline motorhomes because a fuel hose may not be properly secured, creating a gas leak and fire risk.
Mazda is recalling certain 2022-2023 CX-30 and 2023 CX-50 vehicles because the anti-lock brake system hydraulic control unit may be damaged, reducing braking ability and increasing crash risk.
Prevost is recalling 2021-2023 X3-45 Commuter buses because loose seat cushion bolts may allow cushions to detach, increasing injury risk in crashes.
Prevost is recalling 2021-2023 X3-45 Commuter buses because improperly welded seat frames may fail to restrain passengers during a crash.
3M is recalling specific lots of Flexible Prismatic Conspicuity Tape that may not be adequately reflective at certain angles, potentially reducing vehicle visibility.
Nissan is recalling 2023 Frontier and Titan vehicles because a tear in the tire's inner bead can cause rapid pressure loss, increasing crash risk.
Winnebago is recalling 2021–2023 Micro Minnie travel trailers because the spare tire carrier may fail and detach, posing a road hazard and increasing crash risk. Dealers will replace the carrier free of charge.
Luxor Workspaces is recalling approximately 84,700 audiovisual carts that can tip over when loaded with heavy objects like cathode-ray tube televisions. Three children have died and one was seriously injured in tip-over incidents between 2006 and 2016.
Certain 2021-2023 Jeep Wrangler, Gladiator, and Ram 1500 models equipped with 3.0L diesel engines may experience fuel pump failure, which can cause engine stall and increase crash risk. The recall affects approximately 45,832 vehicles.
Field Van is recalling certain 2019-2022 Sprinter vehicles with Warn Winch wireless remotes. Water intrusion into the remote can cause corrosion and unintended winch operation, increasing injury risk.