The Recall Desk

State

South Dakota product recalls

73,190 recalls have nationwide distribution and so reach South Dakota. 2,684 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total
2,684
Critical
401
Severe
567
Most recent
2026-09-23

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.

These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14101–14125 of 75874

  • ModerateFDA (Drugs)·D-0089-2024·2023-11-15

    Hydrocortisone and Acetic Acid Otic Solution recalled for failed specifications

    Taro Pharmaceuticals recalls 11,196 bottles of Hydrocortisone and Acetic Acid Otic Solution nationwide due to failed quality specifications including out-of-spec impurities and lower-than-established assay levels discovered during stability testing.

    Product
    HYDROCORTISONE AND ACETIC ACID — HYDROCORTISONE AND ACETIC ACID (HYDROCORTISONE AND ACETIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0263-2024·2023-11-15

    Fixodent Denture Cream Recalled Due to Improper Storage Conditions

    Family Dollar is recalling 329,044 units of Fixodent denture cream products due to improper storage outside labeled temperature requirements. No illnesses or injuries have been reported.

    Product
    FIXODENT ORG CREAM 2.4OZ, SKU 906018 FIXODENT ADH CREAM WITH SCOPE 2OZ, SKU 906402 FIXODENT ORG CREAM TRAVEL .75OZ, SKU 901239
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-0269-2024·2023-11-15

    Contact Lens Solution Recalled for Improper Storage Temperature

    Family Dollar's MEDIC's CHOICE contact lens solution was distributed between June and October 2023 due to storage outside labeled temperature requirements. Approximately 329,044 units were affected across 22 states.

    Product
    MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ, SKU 998935
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-0242-2024·2023-11-15

    Disposable Surgical Forceps Recalled for Incorrect Expiration Date Labeling

    Stryker Corporation is recalling 2,321 units of Disposable Spetzler-Malis Bipolar forceps due to an error in the product label's expiration date. The label indicates a 54-month shelf life when the actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 23CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-230-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0248-2024·2023-11-15

    Disposable Bipolar Forceps Shelf Life Labeling Error Stryker

    Stryker recalls disposable Spetzler-Malis bipolar forceps due to incorrect shelf life labeling. The label states 54 months but the actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-200-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0256-2024·2023-11-15

    Stryker surgical forceps recall due to incorrect expiration date labeling

    Stryker Corporation is recalling Spetzler-Malis Bipolar forceps due to incorrect shelf-life labeling. The devices are labeled with a 54-month shelf life but actually expire after 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 1.0MM, Catalog Number 6780-230-010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0097-2024·2023-11-15

    Zydus oxybutynin extended-release tablets recalled nationwide for failed stability testing

    Zydus Pharmaceuticals is recalling specific lots of oxybutynin chloride extended-release 10 mg tablets nationwide due to out-of-specification dissolution test results at the 6-month stability timepoint. The affected tablets may not release medication properly.

    Product
    OXYBUTYNIN — OXYBUTYNIN (OXYBUTYNIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0262-2024·2023-11-15

    Family Dollar marijuana test strips recalled over improper storage

    Family Dollar recalled 329,044 at-home marijuana test strips (SKU 900752) due to improper storage outside labeled temperature requirements. Products were distributed across 22 states between June and October 2023.

    Product
    AT HOME MARIJUANA TEST STRIP, SKU 900752
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-0270-2024·2023-11-15

    Oral B Mouth Sore Rinse Recall Due to Improper Storage Conditions

    Family Dollar is recalling approximately 329,044 units of Oral B Mouth Sore Rinse 237ML because the product was stored outside of labeled temperature requirements. No illnesses or injuries have been reported.

    Product
    ORAL B MOUTH SORE RINSE 237ML, SKU 999087
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-0268-2024·2023-11-15

    ARC Teeth Whitening Pen Recalled Due to Improper Storage

    Family Dollar recalls 329,044 units of ARC Teeth Whitening Pen sold between June and October 2023 across 22 states due to improper storage outside temperature requirements.

    Product
    ARC TEETH WHITENING PEN 0.06 FL OZ, SKU 997950
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Drugs)·D-0091-2024·2023-11-15

    Antifungal Powder Recalled Due to Low Active Ingredient Content

    Medline Industries is recalling REMEDY Antifungal powder nationwide because it contains insufficient miconazole nitrate (the active ingredient). The product was shipped before assay testing was complete.

    Product
    REMEDY ANTIFUNGAL — REMEDY ANTIFUNGAL (MICONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0253-2024·2023-11-15

    Surgical forceps recalled due to mislabeled shelf life

    Stryker Corporation is recalling Disposable Spetzler-Malis Bipolar forceps due to a labeling error showing an incorrect expiration date. The label states a 54-month shelf life when the actual shelf life is 36 months.

    Product
    Disposable Spetzler-Malis Bipolar forceps, 20CM SLM DISP BAYONET 1.0MM, Catalog Number 6780-200-010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0266-2024·2023-11-15

    First Response 2 CT Recalled for Improper Temperature Storage

    Family Dollar recalled 329,044 First Response 2 CT units sold between June and October 2023 due to storage outside labeled temperature requirements. The recall affects 22 states.

    Product
    FIRST RESPONSE 2 CT, SKU 902343
    Category
    Medical Device
    Distribution
    23 states
  • SevereNHTSA·23V768000·2023-11-14

    Lonestar Recalls 2021-2023 SV Electric S22 Tractors for Fire Risk

    Lonestar is recalling 2021-2023 SV Electric S22 terminal tractors because a software defect may prevent detection of high-voltage battery malfunctions, increasing fire risk.

    Product
    LONESTAR — LONESTAR SV ELECTRIC S22
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E088000·2023-11-14

    Driver Air Bag Clockspring Recall for Potential Deactivation

    BCS Automotive recalls steering column control modules that may fail and deactivate driver air bags, increasing crash injury risk.

    Product
    AIR BAGS:FRONTAL:DRIVER CLOCKSPRING/SPIRAL CASSETTE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V751000·2023-11-13

    Honda Recalls Acura and Honda Vehicles for Engine Bearing Defect

    Honda is recalling specific Acura and Honda models because a manufacturing error may cause engine bearing wear, leading to stalling or fire.

    Product
    ACURA — ACURA, HONDA TLX, MDX, PILOT, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V766000·2023-11-13

    Triple E RV Recalls 2023-2024 Wonder Motorhomes Due to Fire Risk

    Triple E Recreational Vehicles is recalling 2023-2024 Wonder motorhomes because damaged wire insulation on the 120-volt air conditioner line may cause electrical arcing and increase the risk of a fire.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V764000·2023-11-13

    Terberg Terminal Tractor Recall for Loose Steering Axle Nuts

    Terberg Benschop B.V. is recalling one 2022 YT193 terminal tractor because non-self-locking flange nuts on the steering front axle may come loose, potentially causing a loss of steering or braking.

    Product
    TERBERG BENSCHOP B.V. — TERBERG BENSCHOP B.V. TERMINAL TRACTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V763000·2023-11-11

    Nova Bus LFS Transit Buses Recalled for HVAC Unit Bracket Failure

    Nova Bus (US) Inc. is recalling 2020–2023 LFS transit buses because mounting brackets for the HVAC unit could fail, causing the unit to detach and create a road hazard. Free repairs are available through Nova Bus customer service.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V762000·2023-11-11

    2022 Nova Bus LFS Transit Buses Recalled for Turn Signal Failure

    Nova Bus is recalling certain 2021-2023 LFS transit buses due to defective turn signal wiring that may fail intermittently, increasing crash risk. Free repairs are available.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V761000·2023-11-10

    Prevost Motor Coaches Recalled for Fire Risk in Grid Heater System

    Prevost Car (US) Inc. is recalling 204 certain 2023-2024 H3-45 and X3-45 VIP motor coaches due to loose grid heater cable connections that can cause the relay to overheat, increasing fire risk.

    Product
    PREVOST — PREVOST X3-45, H3-45 VIP, X3-45 VIP, H3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide