The Recall Desk

State

South Dakota product recalls

73,388 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
747
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 747 (28%) are Severe.

These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22226–22250 of 76072

  • HighCPSC·22090·2022-03-02

    ALDI Bee Happy Advent Calendars Recalled for Excessive Lead Paint

    ALDI is recalling Bee Happy 12 Days of Craft Advent Calendars due to lead paint on a brown bell in Day 10 that exceeds the federal lead paint ban. The product poses a risk of lead poisoning if the paint is ingested, particularly for young children.

    Product
    Bee Happy 12 Days of Craft Advent Calendars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0666-2022·2022-03-02

    Bard SureStep Intermittent Catheter Tray recalled for potential leak defect

    C.R. Bard is recalling 2,120 units of the BARD SURESTEP INTERMITTENT CATHETER TRAY (14Fr) due to a potential leak at the catheter-to-drain-bag connection.

    Product
    BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0657-2022·2022-03-02

    Medtronic Endurant Stent Graft Systems: Taper Tip Detachment Risk

    Certain Medtronic Endurant stent graft systems may have taper tips that detach from the delivery system during implant procedures, potentially requiring secondary surgical intervention.

    Product
    Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF ENBF2313C120EE; ENBF2313C120EE; ENBF2313C145EE; ENBF2313C170EE; ENBF2316C120EE; ENBF2316C145EE; ENBF2316C170EE; ENBF2513C120EE; ENBF2513C145EE; ENBF2513C170EE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0675-2022·2022-03-02

    Biomet Shoulder Implant Stem Coating Adhesion Defect Recall

    Biomet is recalling shoulder implant stems due to improper rework of porous plasma coating, which may lack sufficient adhesion strength. Affected units may fail if the coating detaches.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0626-2022·2022-03-02

    Equate Nasal Spray Recalled for Contaminated Excipient Manufacturing Defect

    Perrigo Company PLC is recalling Equate Nasal No Drip Nasal Spray because the product was manufactured with a contaminated excipient that was previously recalled from the supplier.

    Product
    EQUATE NASAL — EQUATE NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0629-2022·2022-03-02

    Perrigo Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling NASAL Maximum Strength Nasal Spray (oxymetazoline HCl 0.05%) due to manufacturing with a contaminated excipient that was itself recalled from the supplier. The recall affects one batch distributed nationwide.

    Product
    NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0599-2022·2022-03-02

    Equate Children's Pain and Fever recalled due to contaminated excipient

    Perrigo Company is recalling Equate Children's Pain and Fever (Acetaminophen) oral suspension nationwide due to manufacturing deviations involving contaminated excipient from a supplier.

    Product
    EQUATE CHILDRENS PAIN AND FEVER — EQUATE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0603-2022·2022-03-02

    Basic Care No Drip Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company is recalling 37,104 bottles of Basic Care No Drip Nasal Spray (oxymetazoline hydrochloride 0.05%) nationwide due to contaminated excipient used during manufacturing. The affected batches were distributed to U.S. consumers.

    Product
    BASIC CARE NO DRIP NASAL — BASIC CARE NO DRIP NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0604-2022·2022-03-02

    Perrigo Severe Congestion Nasal Spray recalled for contaminated excipient

    Perrigo Company is recalling Severe Congestion Nasal Spray, No Drip Plus Menthol because the product was manufactured with a contaminated excipient that was recalled from the supplier.

    Product
    Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Packaged by Perrigo Company for: Big Lots Stores, Inc., P.O. Box 28523, Columbus, OH 43228-0523. NDC: 50594-719-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0570-2022·2022-03-02

    Prevantics Maxi Swabstick Recall Due to Manufacturing Validation Issues

    Professional Disposables International is recalling Prevantics Maxi Swabstick (chlorhexidine gluconate and isopropyl alcohol) due to unvalidated test methods used during manufacturing. The company has not reported any illnesses or injuries.

    Product
    PREVANTICS MAXI SWABSTICK — PREVANTICS MAXI SWABSTICK (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0600-2022·2022-03-02

    Children's Acetaminophen Oral Suspension Recalled for Contaminated Excipient

    Perrigo Company is recalling 561 bottles of Children's Pain & Fever Acetaminophen 160 mg per 5 mL oral suspension due to contamination from a recalled excipient ingredient used during manufacturing.

    Product
    Children's Pain & Fever Acetaminophen, 160 mg per 5 mL Oral Suspension combo pack. DS SR APAP 160MG CHLD BBGM/DF CHRY/GRP. UPC: 3 70030 11637 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0620-2022·2022-03-02

    Oxymetazoline HCl Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling NASAL Maximum Strength No Drip Nasal Spray (oxymetazoline HCl 0.05%) because the product was manufactured with a contaminated excipient from a recalled supplier.

    Product
    NASAL — NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0572-2022·2022-03-02

    Prevantics Swabstick Chlorhexidine Recall Due to Test Validation Uncertainty

    Professional Disposables International is recalling Prevantics Swabstick (chlorhexidine gluconate and isopropyl alcohol) products nationwide due to uncertain validation of the test methods used during manufacturing.

    Product
    PREVANTICS SWABSTICK — PREVANTICS SWABSTICK (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0575-2022·2022-03-02

    Dr. Reddy's Azacitidine Injectable Drug Recalled for Failed Stability

    Dr. Reddy's Laboratories is recalling Azacitidine 100mg injectable vials nationwide due to failed stability specifications. Multiple lot numbers distributed across the United States are affected.

    Product
    AZACITIDINE — AZACITIDINE (AZACITIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0590-2022·2022-03-02

    DG Health Children's Acetaminophen Recalled for Contaminated Excipient

    Perrigo Company is recalling DG Health Children's Pain and Fever (acetaminophen) oral suspension because the product was manufactured with a contaminated excipient that was itself recalled by its supplier.

    Product
    DG HEALTH CHILDRENS PAIN AND FEVER — DG HEALTH CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0595-2022·2022-03-02

    Infants Pain and Fever Acetaminophen recalled for contaminated excipient

    Perrigo Company is recalling Infants Pain and Fever Acetaminophen Infant Dye Free Grape Oral Suspension due to contaminated excipient used in manufacturing. The recall affects 1,296 bottles distributed nationwide.

    Product
    INFANTS PAIN AND FEVER — INFANTS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0587-2022·2022-03-02

    Good Sense Acetaminophen Child Suspension Recalled Due to Contaminated Excipient

    Perrigo is recalling Good Sense Pain and Fever acetaminophen child oral suspension (160mg/5ml, 4 FL OZ bottles) nationwide because the product was manufactured with a contaminated excipient that was recalled by the supplier.

    Product
    GOOD SENSE PAIN AND FEVER — GOOD SENSE PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0571-2022·2022-03-02

    Prevantics Swab Drug Recall for Test Method Validation Deficiency

    Professional Disposables International, Inc. is recalling Prevantics Swab (chlorhexidine gluconate and isopropyl alcohol) due to cGMP deviations involving inadequate validation of manufacturing test methods. The product was distributed nationwide in the USA and Puerto Rico.

    Product
    PREVANTICS SWAB — PREVANTICS SWAB (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0577-2022·2022-03-02

    Bortezomib 3.5 mg Vials Recalled Due to Failed Stability Specifications

    Dr. Reddy's Laboratories is recalling Bortezomib 3.5 mg single-dose vials nationwide due to failed stability specifications. Approximately 2,980 vials of lot H210233 (expiration 3/1/2023) are affected.

    Product
    Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-865-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0619-2022·2022-03-02

    Perrigo Nasal Oxymetazoline Spray Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling approximately 10,800 bottles of NASAL Maximum Strength No Drip Nasal Spray (Oxymetazoline HCl 0.05%) nationwide due to manufacturing with a contaminated excipient supplied by their ingredient vendor.

    Product
    NASAL — NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0611-2022·2022-03-02

    Target Severe Congestion Nasal Spray recalled for contaminated excipient

    Perrigo Company is recalling Target Severe Congestion Nasal Spray (Oxymetazoline HCl 0.05%) because it was manufactured with a contaminated excipient that had been recalled from the supplier.

    Product
    Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Dist. by Target Corp., Mpls., MN 55403. NDC 11673-935-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0606-2022·2022-03-02

    DG Health Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling DG Health Nasal Spray (Oxymetazoline HCl 0.05%) distributed nationwide because the product was manufactured with a contaminated excipient that was itself recalled from the supplier.

    Product
    DG HEALTH NASAL — DG HEALTH NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0589-2022·2022-03-02

    Equate Children's Pain and Fever Acetaminophen Recalled for Contaminated Excipient

    Perrigo Company is recalling Equate Children's Pain and Fever acetaminophen suspension due to contamination from a recalled excipient used during manufacturing. The affected batch was distributed nationwide.

    Product
    EQUATE CHILDRENS PAIN AND FEVER — EQUATE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0605-2022·2022-03-02

    CareOne Severe Congestion Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company is recalling CareOne Severe Congestion Nasal Spray due to contaminated excipient used during manufacturing. The nasal spray was made with an excipient that had been recalled from the supplier.

    Product
    CAREONE SEVERE CONGESTION NASAL — CAREONE SEVERE CONGESTION NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0596-2022·2022-03-02

    Infants Pain and Fever acetaminophen recalled for contaminated excipient

    Perrigo Company is recalling Infants Pain and Fever acetaminophen oral suspension (160mg/5ml) distributed nationwide due to contamination from a recalled excipient supplier. The product was manufactured with a contaminated ingredient that does not meet manufacturing standards.

    Product
    INFANTS PAIN AND FEVER — INFANTS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide