The Recall Desk

State

South Dakota product recalls

73,363 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 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17776–17800 of 76047

  • HighCPSC·23723·2023-02-09

    Model Year 2023 Can-Am Side-by-Side Vehicles Recalled for Fire Hazard

    BRP is recalling about 3,310 Model Year 2023 Can-Am side-by-side vehicles because a defective fuel hose assembly could leak fuel and create a fire hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.

    Product
    Model Year 2023 Can-Am side-by-side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23117·2023-02-09

    Skip Hop Silver Lining Cloud Activity Gyms Recalled for Choking Hazard

    Skip Hop is recalling Silver Lining Cloud Activity Gyms because raindrops attached to the included cloud toy can detach and pose a choking hazard to children. No injuries have been reported.

    Product
    Silver Lining Cloud Activity Gyms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23725·2023-02-09

    LiftMaster myQ Garage Door Control Panels Recalled for Entrapment Hazard

    Chamberlain Group is recalling about 96,400 LiftMaster myQ garage door control panels because the secondary entrapment protection system can fail, allowing the garage door to close even when an obstruction is present. No injuries have been reported in the U.S.

    Product
    LiftMaster myQ Garage Door Control Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V063000·2023-02-09

    Freightliner Recalls Coronado Trucks Due to Loose Upper Bunk Bolts

    Daimler Trucks North America is recalling 2021-2023 Freightliner Coronado vehicles because upper bunk mounting bolts may loosen, posing an injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER CORONADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23118·2023-02-09

    IKEA ODGER Swivel Chairs Recalled Due to Leg Base Breakage and Fall Risk

    IKEA is recalling about 12,000 ODGER Swivel Chairs in anthracite because the leg base can break, creating a fall hazard. Four reports of leg base breaking have been received, including two reports of consumer injuries from falls.

    Product
    IKEA ODGER Swivel Chairs, Anthracite
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V061000·2023-02-09

    Motorhome Cooktops May Leak Gas and Create Fire Risk

    Forest River is recalling certain 2022-2023 Coachmen motorhomes with faulty cooktops. The burner tubes may fracture and leak gas, creating a fire hazard.

    Product
    COACHMEN — COACHMEN GALLERIA, BEYOND, NOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23726·2023-02-09

    E-Z-GO Personal Transportation Vehicles Recalled for Fire Hazard

    Textron Specialized Vehicles is recalling about 143,000 E-Z-GO personal transportation vehicles because the electronic board powering the USB port can overheat and ignite, creating a fire hazard. Consumers should stop using the vehicles immediately and contact Textron for a free repair.

    Product
    E-Z-GO Personal Transportation Vehicles (PTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V060000·2023-02-09

    RAM pickup and cab chassis trucks recalled for engine compartment fire risk

    Chrysler is recalling 2021–2023 RAM 2500, 3500, 4500, and 5500 Cummins diesel trucks due to an electrical short in the heater grid relay that can cause engine compartment fires. Owners should park outside and away from structures until repairs are completed.

    Product
    RAM — RAM 3500, 2500, 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V059000·2023-02-09

    RAM 1500 and 2500 Rearview Display May Fail When in Reverse

    Certain 2021-2023 RAM 1500 and 2023 RAM 2500 vehicles have a software defect that may prevent the rearview image from displaying when in reverse, reducing driver visibility.

    Product
    RAM — RAM 1500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23724·2023-02-09

    WeeSprout Baby Sleep Sacks Recalled Due to Choking Hazard

    WeeSprout baby sleep sacks are being recalled because the zipper can detach, posing a choking hazard to infants. The company has received 17 reports of zipper detachment but no injuries have been reported.

    Product
    Baby Sleep Sacks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0246-2023·2023-02-08

    First Aid Kit with Burn Cream Recalled for Bacterial Contamination

    GFA Production is recalling Adventure First Aid 1.0 kits containing Easy Care After Burn Cream due to confirmed bacterial contamination found in FDA testing. The affected product was distributed nationwide and in Canada.

    Product
    Adventure First Aid 1.0, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0213
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0250-2023·2023-02-08

    Easy Care First Aid Kit Recalled for Bacterial Contamination

    GFA Production is recalling Easy Care First Aid Kits distributed nationwide and in Canada due to bacterial contamination of included After Burn Cream packets. The FDA confirmed the presence of Bacillus lichenformis and Bacillus sonorensis.

    Product
    Easy Care First Aid Class A ANSI 25 Person, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2150
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0244-2023·2023-02-08

    Easy Care first aid burn cream recalled for microbial contamination

    Easy Care first aid burn cream distributed nationwide and in Canada is recalled due to FDA-detected contamination with Bacillus lichenformis and Bacillus sonorensis. The product should not be used.

    Product
    Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and lidocaine hydrochloride 0.5%), 0.9 g (0.03 oz) packets packaged in boxes of 10, Treatment for Burns, Made in China for Adventure Ready Brands, 944 Industrial Park Rd., Littleton, NH 03561, NDC 90107-0210, Product #…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0965-2023·2023-02-08

    CADD Infusion Administration Set Recalled for Delivery Failure and False Alarms

    Smiths Medical is recalling CADD Administration Sets due to tubing occlusion that can prevent medication delivery and false pump alarms. This FDA Class I recall affects 214,668 units worldwide.

    Product
    CADD Administration Set, List Numbers: a) REF 21-7600-24, b) REF 21-7609-24, c) REF 21-7624-24, d) REF 21-7649-24, e) REF 21-7600-24JP, f) REF 21-7609-24JP, g) REF 21-7624-24JP, h) REF 21-7649-24JP Computerized Ambulatory Delivery Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0964-2023·2023-02-08

    CADD Infusion Administration Sets Recalled for Delivery Failure and Alarms

    FDA recalls 726,878 CADD Infusion Administration Sets due to potential tubing occlusion causing delivery failure and false alarm warnings.

    Product
    CADD Administration Set, List Numbers: a) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24, d) REF 21-7308-24JP, e) REF 21-7309-24JP. Computerized Ambulatory Delivery Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0963-2023·2023-02-08

    CADD Infusion Administration Sets Recalled for Tubing Occlusion and False Alarms

    Smiths Medical is recalling CADD Administration Sets for two issues: tubing may become blocked, preventing medication delivery, and devices may show false alerts about disposable attachment status.

    Product
    CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4) REF 21-7321-24, 5) REF 21-7322-24, 6) REF 21-7323-24, 7) REF 21-7324-24, 8) REF 21-7333-24, 9) REF 21-7336-24, 10) REF 21-7339-24, 11) REF 21-7343-24, 12) REF 21-7349-24…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0248-2023·2023-02-08

    FDA Recalls Easy Care First Aid Kits for Bacterial Contamination

    GFA Production's Easy Care First Aid 25 Person kits are being recalled nationwide due to contamination with Bacillus bacteria. The affected first aid cream packets could pose a risk if applied to open wounds.

    Product
    Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2129
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0253-2023·2023-02-08

    Easy Care First Aid Kit Recalled for Microbial Contamination

    The FDA is recalling Easy Care First Aid kits containing After Burn Cream due to microbial contamination. The affected product was distributed nationwide and in Canada with lot number W06H15 (expiration August 15, 2024).

    Product
    Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2131
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0252-2023·2023-02-08

    CVS First Aid Home Burn Cream Packets Recalled for Bacterial Contamination

    CVS First Aid Home, First Aid Kit burn cream packets have been recalled due to bacterial contamination. The product contains Bacillus lichenformis and Bacillus sonorensis bacteria, creating a risk when applied to wounds or burns.

    Product
    CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 2980-0700
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0249-2023·2023-02-08

    Easy Care First Aid Kits Recalled for Bacterial Contamination

    GFA Production is recalling Easy Care First Aid 10 Person First Aid Kits because the included After Burn Cream packets are contaminated with Bacillus bacteria. Contamination was identified through FDA laboratory testing.

    Product
    Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2128
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0245-2023·2023-02-08

    First Aid Kit Product Recalled Due to Bacterial Contamination

    A first aid kit containing topical burn cream has been recalled due to bacterial contamination with Bacillus species. The product (Lot W06I20) was distributed nationwide and in Canada.

    Product
    Adventure Marine 150, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 1015-0150
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0966-2023·2023-02-08

    CADD Administration Sets recall for delivery failure and false alarms

    Smiths Medical is recalling CADD Administration Sets due to potential tubing occlusion causing medication underdelivery and false alarm errors. The FDA classified this as a Class I recall affecting nearly 48 million units worldwide.

    Product
    CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24, 3) REF 21-7302-24, 4) REF 21-7308-24, 5) REF 21-7309-24, 6) REF 21-7310-24, 7) REF 21-7322-24, 8) REF 21-7323-24, 9) REF 21-7324-24, 10) REF 21-7333-24, 11) REF 21-7343-24, 12) REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0962-2023·2023-02-08

    CADD Administration Set recall: medication underdelivery and false alarms

    Smiths Medical is recalling 1.6 million CADD Infusion System Administration Sets due to tubing occlusion causing medication underdelivery and false alarm conditions affecting patients worldwide.

    Product
    CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0929-2023·2023-02-08

    SARS-CoV-2 Antigen Rapid Test Kits Recalled for Lack of FDA Authorization

    Universal Meditech Inc. is recalling approximately 56,300 SARS-CoV-2 Antigen Rapid Test Kits distributed without FDA approval, clearance, or Emergency Use Authorization. Products were distributed nationwide in California and Texas.

    Product
    Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green and white box under the brand DiagnosUS, and, White box without brand name labeled as "SARS -COV-2 ANTIGEN DEVELOPMENT MADE IN USA ORAL SWAB…
    Category
    Medical Device
    Distribution
    Distributed nationwide