The Recall Desk

State

South Dakota product recalls

72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8201–8225 of 75667

  • HighFDA (Drugs)·D-0190-2025·2025-01-15

    Duloxetine Drug Recall Due to Manufacturing Impurity Levels

    Rising Pharma recalls Duloxetine DR Capsules 60 mg nationwide due to N-nitroso-duloxetine impurity levels exceeding FDA limits. Affected batches were distributed nationwide; check lot numbers on bottle labels for affected product.

    Product
    Duloxetine DR Capsules USP 60 mg, a) 30 count (NDC 57237-019-30) and b) 1000 count (NDC 57237-019-99) bottles; Distributed by: Rising Pharm Holdings, Inc., East Brunswick, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0808-2025·2025-01-15

    Aerin Medical VivAer Stylus Recall: Programming Error Causes Device Misidentification

    Aerin Medical is recalling 479 units of VivAer Stylus (Lot #10235) due to incorrect programming in units from a single lot. When connected to the Aerin Console, affected devices will be incorrectly identified as RhinAer Stylus.

    Product
    Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0187-2025·2025-01-15

    Colchicine Capsules Recalled Due to Failed Dissolution Specifications

    Granules Pharmaceuticals is recalling Colchicine 0.6 mg capsules nationwide due to failed dissolution specifications detected during stability testing. Patients should contact their healthcare provider for guidance.

    Product
    COLCHICINE — COLCHICINE (COLCHICINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0184-2025·2025-01-15

    Clobazam Tablets Recalled for Foreign Tablet Contamination

    Amerisource Health Services LLC is recalling Clobazam 10 mg tablets due to the presence of foreign tablets or capsules in some packages. The recall affects 5,178 cartons with Lot #1019594 distributed nationwide.

    Product
    CLOBAZAM — CLOBAZAM (CLOBAZAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0186-2025·2025-01-15

    Progesterone Injection Recalled Nationwide for Glass Particulate Matter

    Eugia US LLC is recalling Progesterone Injection due to a market complaint of glass particles found in vials. The affected batch poses a potential risk to patients who receive injections from contaminated vials.

    Product
    PROGESTERONE — PROGESTERONE (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0809-2025·2025-01-15

    Xhibit Telemetry Receiver may shut down, causing temporary loss of patient monitoring

    Spacelabs Healthcare's Xhibit Telemetry Receiver (Model 96280) may experience a Windows proxy issue causing the system to restart and go offline for 1-1.5 minutes, creating a temporary gap in patient monitoring.

    Product
    Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
    Category
    Medical Device
    Distribution
    44 states
  • HighNHTSA·25V009000·2025-01-15

    Marion Body Works Recalls 2024 Spartan Fire Metro Star Vehicles

    Marion Body Works is recalling 2024 Spartan Fire Metro Star vehicles because a missing mechanical stop may allow the cab tilt cylinder to overextend, increasing the risk of injury.

    Product
    MARION BODY WORKS — MARION BODY WORKS SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0815-2025·2025-01-15

    Tec 820 ISO Anesthesia Vaporizers can deliver less anesthetic than dial setting

    GE Medical Systems is recalling 644 Tec 820 ISO Anesthesia Vaporizers due to a manufacturing issue that causes them to deliver less anesthetic than the dial setting indicates. Distributed nationwide and globally.

    Product
    Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0183-2025·2025-01-15

    Methadone Hydrochloride Tablets recalled for illegible product identification

    West-Ward Columbus is recalling Methadone Hydrochloride Tablets, 5mg, in unit-dose packaging due to illegible product identification on individual tablets. Lot AC2556A was distributed nationwide.

    Product
    METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E002000·2025-01-14

    GKN Recalls Replacement Driveshafts for BMW Mini and Land Rover Vehicles

    GKN Automotive is recalling replacement driveshafts for specific BMW Mini and Land Rover models because they can crack or break, increasing the risk of a crash.

    Product
    POWER TRAIN:DRIVELINE:DRIVESHAFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E001000·2025-01-13

    Nivion NSP01 Charger Adapter Recall for Electrical Arcing Risk

    N&B Mobility Solutions is recalling Nivion NSP01 charger adapters due to electrical arcing and shock risks. Owners should contact Nivion for a free replacement.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V007000·2025-01-13

    Winnebago spare tire carrier mounting bolts may loosen and detach

    Winnebago is recalling certain 2025 Minnie Winnie and Spirit motorhomes because the spare tire carrier mounting bolts may loosen, allowing the carrier to detach.

    Product
    WINNEBAGO — WINNEBAGO SPIRIT, MINNIE WINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V006000·2025-01-13

    Kia Sorento software error may disable low beams and taillights

    Kia is recalling certain 2024-2025 Sorento vehicles because a Body Domain Control Unit software error may cause a loss of low beam headlights and taillights.

    Product
    KIA — KIA SORENTO, SORENTO PHEV, SORENTO HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2025·2025-01-11

    Bestway Recalls Frozen Chicken Taquitos Due to Metal Contamination

    Bestway Sandwiches Inc. is recalling frozen chicken and cheese taquitos due to possible metal contamination. One consumer reported a dental injury.

    Product
    Bestway Sandwiches Inc. — Bestway Sandwiches Inc. Recalls Frozen Chicken And Cheese Taquito Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0371-2025·2025-01-08

    Kowalski's Garden Salad Recalled for Potential Salmonella Contamination

    Kowalski's Garden Salad (14 oz) is recalled due to potential Salmonella contamination in cucumbers. The recall affects 206 units distributed across 11 states with use/sell by dates November 6-15, 2024.

    Product
    Kowalski's Garden Salad Net Wt. 14oz. Keep Refrigerated. UPC 7 95631-89335 9. Containing Lettuce, Cucumber, Tomatoes, Broccoli, Cheddar Cheese, Onion, Hard Cooked Eggs, Carrots, Roasted Sunflower Kernels.
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0319-2025·2025-01-08

    Napoleonas Torte recalled for undeclared allergens and food additives

    Lithuanian Bakery is recalling Napoleonas Torte due to undeclared allergens (milk, soy, wheat) and undeclared additives (sulfites, yellow 5 and 6). The product was distributed at retail stores in Iowa, Illinois, Kansas, Missouri, Minnesota, Nebraska, and South Dakota.

    Product
    Napoleonas Torte packaged under the following sizes: 1. Small, Net Wt 1.25 lbs. (sub ingredients contain wheat, yellow #5 and #6, and sulfites not declared on final product label) 2. Medium, Net Wt 2.75 lbs. (sub ingredients contain yellow #5 and #6 not declared on final prod
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0369-2025·2025-01-08

    Bacon Avocado Wrap Recalled Due to Potential Salmonella in Cucumbers

    RUSS DAVIS WHOLESALE is recalling Bacon Avocado Wraps sold under Crazy Fresh and quick & easy brands due to potential Salmonella contamination in cucumbers. 491 units were distributed across 11 states.

    Product
    Bacon Avocado Wrap, Net Wt 9.9oz. Keep Refrigerated. UPC 7 95631-81038 7. Containing Flour Tortilla,Carrots, Lettuce, Cheddar Cheese, Cucumber, Guacamole, Bacon Bits, Ranch Dressing, Spinach, Cream Cheese. Sold under the following brands: 1. Crazy Fresh 2. quick & eas
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0170-2025·2025-01-08

    FORCE FOREVER supplement tablets recalled for undisclosed drugs

    GNMart LLC is recalling FORCE FOREVER 400mg tablets nationwide after the FDA found the product contains undisclosed Diclofenac and Dexamethasone. The Class I recall affects all lots of this dietary supplement product.

    Product
    FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0370-2025·2025-01-08

    Salmonella in Cucumbers in Crazy Fresh Turkey Havarti Wraps

    Russ Davis Wholesale is recalling Crazy Fresh Turkey Havarti Wraps due to potential Salmonella contamination in cucumbers. The product was distributed in multiple US states with sell-by dates between November 9-16, 2024.

    Product
    Crazy Fresh Turkey Havarti Wrap, Net Wt 6.8oz. Keep Refrigerated. UPC 7 95631-81149 0. Containing Flour Tortilla, Cooked Turkey Breast, Roasted Tomatoes, Havarti cheese, Mayonnaise, Lettuce, Onion, Cucumber.
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0367-2025·2025-01-08

    FDA Recalls Cucumbers from Russ Davis Wholesale Due to Salmonella Risk

    Russ Davis Wholesale is recalling cucumbers distributed across 11 U.S. states due to potential Salmonella contamination. A total of 1,595 units are affected.

    Product
    Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico. 2. Peak Cucumber Item 08009, 5 LB. Product of Mexico. 3. Cucumber Super Select Item 22200, 24 count. Product of Mexico. 4. Cucumber Item 22201, 5 lb. Produ
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0368-2025·2025-01-08

    Garden Salad with Dressing Recalled Due to Potential Salmonella Contamination

    Russ Davis Wholesale is recalling garden salads sold under Crazy Fresh and quick & easy brands due to potential Salmonella contamination in cucumbers. Affected products have sell-by dates of November 6-16, 2024.

    Product
    Garden Salad w/Ranch Dressing, Net Wt 9oz. Keep Refrigerated. UPC 7 95831-81023 3. Containing Lettuce, tomatoes, cucumbers, cheddar cheese, carrots and hard cooked egg. Sold under the following brands: 1. Crazy Fresh 2. quick & easy, Ready to Enjoy
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0782-2025·2025-01-08

    Medical Device Kits Recalled for Non-Sterile Surgical Components

    Medline Industries is recalling See DocMan custom convenience kits that contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 48,655 units were distributed worldwide.

    Product
    See DocMan
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0793-2025·2025-01-08

    Medline custom surgical procedure kits recalled for non-sterile components

    Medline is recalling 182 custom surgical procedure kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. The kits were distributed in the US, UAE, and Canada.

    Product
    Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF, REF DYNJ0867145G; 2) CERVICAL SPINE PACK HUM-LF, REF DYNJ35184F; 3) ANTERIOR CERVICAL-CORPECTOMY, REF DYNJ904827.
    Category
    Medical Device
    Distribution
    Distributed nationwide