The Recall Desk

State

South Dakota product recalls

72,913 recalls have nationwide distribution and so reach South Dakota. 2,681 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total
2,681
Critical
401
Severe
565
Most recent
2026-09-02

Of the 2,681 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 565 (21%) are Severe.

These figures cover only the 2,681 recalls whose distribution notice names South Dakota specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1701–1725 of 75594

  • SevereFDA (Drugs)·D-0545-2026·2026-05-27

    Erythromycin 500 mg Tablets Recalled for Impurity Above Limits

    Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.

    Product
    ERYTHROMYCIN — ERYTHROMYCIN (ERYTHROMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0544-2026·2026-05-27

    Erythromycin Tablets Recalled for Impurity Above Acceptable Limits

    Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.

    Product
    ERYTHROMYCIN — ERYTHROMYCIN (ERYTHROMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0817-2026·2026-05-27

    Blackstone parmesan ranch seasoning made with recalled milk powder

    Blackstone Parmesan Ranch Seasoning in 7.3 oz containers is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.

    Product
    Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz (207g). UPC 7 17604-04106 2. Manufactured for North Atlantic Imports, LLC, Logan, UT 84321.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0836-2026·2026-05-27

    Fisher Tex Mex Trail Mix recalled over potential Salmonella presence

    Fisher Tex Mex Trail Mix in 30 oz plastic jars is being recalled over the potential presence of Salmonella. 606 cases are affected.

    Product
    Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941, 6 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V343000·2026-05-27

    Ford Explorer, Ranger and Bronco engines may fail during driving

    Ford is recalling certain 2025-2026 Explorer, Ranger and Bronco vehicles because the engine may fail, resulting in a loss of drive power. 1,536 vehicles are affected.

    Product
    FORD — FORD BRONCO, RANGER, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0818-2026·2026-05-27

    PS Seasoning Save A Lot bind made with recalled milk powder

    PS Seasoning PSW21585 Save A Lot Bind 50# is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 992.5 lbs are affected.

    Product
    PSW21585 Save A Lot Bind 50#, Part #: 20009709. PS Seasoning & Spices 216 W Pleasant St Iron Ridge, WI 53035.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2202-2026·2026-05-27

    Swan-Ganz Catheters Models 131F7 Through AIQSGF8 Recalled Nationwide

    Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.

    Product
    Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0832-2026·2026-05-27

    Southern Style Nuts hunter mix jars recalled over potential Salmonella

    Southern Style Nuts Hunter Mix in 30 oz plastic jars is being recalled over the potential presence of Salmonella. 30,515 cases are affected.

    Product
    Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302, 4 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0814-2026·2026-05-27

    Ellsworth sour cream and onion seasoning made with recalled milk powder

    Ellsworth Sour Cream + Onion Seasoning from PS Seasoning is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.

    Product
    Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V344000·2026-05-27

    Ford Expedition and Lincoln Navigator seat belts may lock inadvertently

    Ford is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles because the front seat belt pretensioner may inadvertently lock the belt so it cannot retract or extend.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0831-2026·2026-05-27

    Southern Style Nuts gourmet hunter mix recalled over potential Salmonella

    Southern Style Nuts Gourmet Hunter Mix in 23 oz and 36 oz plastic jars is being recalled over the potential presence of Salmonella. 33,176 cases and 22 displays are affected.

    Product
    Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC 085839071483. 23 oz 6 jars per case case and 96 jars per display. 36 oz 6 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·26V341000·2026-05-27

    Toyota and Lexus instrument clusters may fail to display warnings

    Toyota is recalling certain Lexus UX Hybrid, Lexus GX, Toyota Mirai and Land Cruiser Hybrid vehicles because the instrument panel cluster may fail to display certain warnings or indicators.

    Product
    LEXUS — LEXUS, TOYOTA GX, UX HYBRID, LAND CRUISER HYBRID, MIRAI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V340000·2026-05-27

    Ford Maverick and Bronco Sport Front Control Arm Ball Joint Detachment Recall

    Ford is recalling certain 2021–2026 Bronco Sport and 2022–2026 Maverick vehicles due to potentially loose or improperly installed front lower control arm ball joints that could disconnect from the wheel knuckle, risking loss of vehicle control and crashes.

    Product
    FORD — FORD MAVERICK, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2209-2026·2026-05-27

    Tangent Single Use Digital Catheter Recalled for Distal Shaft Fractures

    Tangent Endoscopy is recalling its Tangent Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) due to fractures observed at the distal shaft tip without complete detachment, posing a risk during endoscopic procedures.

    Product
    Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0800-2026·2026-05-27

    VitaminAlly women's multivitamin drops with iron recalled over manufacturing deviations

    VitaminAlly Liposomal Women's Liquid Multivitamin Drops with Iron are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2214-2026·2026-05-27

    Medtronic GUNDRY Retrograde Cannula Model 94113T sterile barrier recall

    Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.

    Product
    Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2215-2026·2026-05-27

    Medtronic GUNDRY Retrograde Cannula vascular catheter sterile barrier breach

    Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94115T) cardiopulmonary bypass vascular catheters due to potential sterile barrier breach. The affected product has been distributed worldwide.

    Product
    Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0797-2026·2026-05-27

    VitaminAlly womens 50+ multivitamin drops recalled over manufacturing deviations

    VitaminAlly Liposomal Womens 50+ Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0806-2026·2026-05-27

    VitaminAlly liposomal D3 and B12 spray recalled over manufacturing deviations

    VitaminAlly Liposomal D3+B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0803-2026·2026-05-27

    VitaminAlly iron-free women's multivitamin drops recalled over manufacturing deviations

    VitaminAlly Liposomal Women's Liquid Multivitamin Drops, iron free, are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2219-2026·2026-05-27

    Medtronic DLP Retrograde Cannula Cardiopulmonary Bypass Catheter Recall

    Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94913), a cardiopulmonary bypass vascular catheter, due to a potential sterile barrier breach.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2225-2026·2026-05-27

    Philips Azurion X-Ray Systems Table Movement Control Defect Recall

    Philips Azurion X-ray imaging systems may experience impaired table movement due to mechanical wear in the Float Tabletop control. The control module defect could affect longitudinal and transverse table positioning during medical procedures.

    Product
    Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 722229. 2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230. 3.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0796-2026·2026-05-27

    VitaminAlly FulviLife Complex recalled over manufacturing practice deviations

    VitaminAlly FulviLife Complex oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    FulviLife Complex. Dosage:2 tablespoons (30mL). Liquid. Packaging: Plastic Bottle. Net Volume:16 fl oz (480 ml). Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2026·2026-05-27

    Medtronic DLP Retrograde Cannula 15FR Model 94665 Sterile Barrier

    Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0808-2026·2026-05-27

    VitaminAlly liposomal sleep spray recalled over manufacturing practice deviations

    VitaminAlly Liposomal Sleep Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225
    Category
    Food
    Distribution
    Distributed nationwide