State

South Dakota product recalls

73,584 recalls have nationwide distribution and so reach South Dakota. 2,686 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total: 2,686
Critical: 401
Severe: 747
Most recent: 2026-10-14

Of the 2,686 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.

Which agencies issued them

These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

726–750 of 76270

HighFDA (Devices)·Z-3045-2026·2026-09-09
AVID Medical Recalls Neurological Sponges Due to Endotoxin Variability
AVID Medical, Inc. is recalling specific lots of Ritmed Neurological Sponges Non-Sterile due to potential unexpected variability in endotoxin levels.
Product
1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5) BMHM NEURO PACK, (kit) BMHT016-05; 6) LUMBAR PACK, (kit) BMHT112-03; 7) NEURO LAMINECTOMY PACK, (kit) DGNE75; 8) NEURO LAMINECTOMY PACK, (kit)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0815-2026·2026-09-09
Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3079-2026·2026-09-09
Medline Ortho Aspiration Kits Recalled for Potential Contamination
Medline is recalling Ortho Aspiration Kits containing BD ChloraPrep applicators due to packaging seal defects that may allow contamination.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ORTHO ASPIRATION KIT DYKM1636A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3051-2026·2026-09-09
Medline IVS Blood Culture Kits Recalled for Sterility Breach
Medline is recalling 17,750 IVS Blood Culture Kits nationwide due to potential packaging defects that may compromise sterility.
Product
Medline Convenience Kits: 1) IVS BLOOD CULTURE KIT, Model Number: DYNDH1920; 2) IVS BLOOD CULTURE KIT, Model Number: DYNDH1920A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3065-2026·2026-09-09
Baxter Novum IQ Syringe Pump Software Issue Recall
Baxter Healthcare is recalling 14,601 Novum IQ Syringe Pumps due to a software issue that may occur during multi-syringe infusions.
Product
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0813-2026·2026-09-09
Baxter Recalls CARDENE IV Nicardipine Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of CARDENE IV (Nicardipine Hydrochloride) injection due to CGMP deviations. The recall covers products distributed in the US, Puerto Rico, and Chile.
Product
CARDENE IV — CARDENE IV (NICARDIPINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26V581000·2026-09-09
Ford Recalls 2026 Explorers Due to Passenger Air Bag Deployment Defect
Ford is recalling 2026 Explorer vehicles because the passenger air bag may not deploy properly in a crash, increasing injury risk.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0811-2026·2026-09-09
Baxter Recalls Vasopressin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
VASOPRESSIN IN 0.9% SODIUM CHLORIDE — VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN IN 0.9% SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3083-2026·2026-09-09
Boston Scientific Recalls LUX-Dx Insertable Cardiac Monitor Server Software
Boston Scientific is recalling LUX-Dx Insertable Cardiac Monitor server software due to potential delays in Atrial Fibrillation Burden Alert notifications, which may delay clinical evaluation.
Product
LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS ANZ, Model Number 7248, All Versions (Current 7.7)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3064-2026·2026-09-09
Johnson & Johnson Recalls HEALON Viscoelastic Products Due to Surgical Instructions
Johnson & Johnson is recalling HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products because surgical instructions may not adequately warn against forcing the cannula, which could cause eye injury.
Product
HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF: 10301012 (EU); HEALON DUET PRO II, REF: 10301016 (EU)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3055-2026·2026-09-09
Medline Arterial Line Insertion Kits Recalled for Sterility Breach
Medline is recalling 1,840 Arterial Line Insertion Kits due to potential packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) ARTERIAL LINE INSERTION KIT, Model Number: ART1295
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0818-2026·2026-09-09
Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3091-2026·2026-09-09
Fresenius Recalls Granuflo Dry Acid Concentrate Due to Discoloration
Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to complaints of blue-green discoloration in the product.
Product
GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B; 0FD3251-3B; Dry Acid Concentrate for Bicarbonate Hemodialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3078-2026·2026-09-09
Medline Recalls Cataract Preop Kits with Potentially Contaminated Applicators
Medline is recalling specific lots of Cataract Preop Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could allow contamination.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT PREOP KIT DYKS1583A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3074-2026·2026-09-09
Medline Convenience Kits Recalled Due to Potential Applicator Seal Defects
Medline is recalling specific lots of convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could allow contamination.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators DELUXE PRE OP KIT DYKS2018 GENERAL PREOP KIT DYKS1584A PRE OP KIT DYKS1216I PRE-OP KIT DYKM1398B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3081-2026·2026-09-09
Boston Scientific Recalls LUX-Dx Insertable Cardiac Monitor Server Software
Boston Scientific is recalling LUX-Dx Insertable Cardiac Monitor server software due to potential delays in Atrial Fibrillation Burden Alerts, which may delay clinical evaluation.
Product
LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3044-2026·2026-09-09
AVID Medical Recalls Halyard Kits Due to Endotoxin Variability
AVID Medical, Inc. is recalling 11,763 Halyard medical convenience kits due to potential unexpected variability in endotoxin levels.
Product
Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit) ACEN89-02; 3) BACK PACK, Model/Item Number (kit) ALBK51-01; 4) DR DERIAN SPINE PACK SNEDHCPDH, Model/Item Number (kit) DGSP71; 5) BASIC PACK DR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3054-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 434,595 convenience kits nationwide due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) IV START KIT, Catalog Number: DYNDV2520; 2) PERIPHERAL LAB BLOOD CULTURE KIT, Catalog Number: DYNDH1983A; 3) PEDI EMERGENCY TRAY-PURPLE, Catalog Number: ACC010157C; 4) PEDS EMERGENCY TRAY- GREEN, Catalog Number: ACC010158C; 5) PEDI EMERGENCY…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3067-2026·2026-09-09
Medline Convenience Kits Recalled Due to Potential Applicator Seal Defects
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT DYKS1476A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3050-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline Industries is recalling 58,037 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) DYKM1414, Catalog Number: DYKM1414; 2) DYKM1414, Catalog Number: DYKM1414; 3) DYNDH1462A, Catalog Number: DYNDH1462A; 4) DYNJ38145F, Catalog Number: DYNJ38145F; 5) DYNJ63199A, Catalog Number: DYNJ63199A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3077-2026·2026-09-09
Medline Convenience Kits Recalled Due to Potential Packaging Seal Defects
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that may allow contamination.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators C-SECTION PREP DYNJ32702B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3070-2026·2026-09-09
Medline Convenience Kits Recalled for Potential ChloraPrep Applicator Contamination
Medline is recalling convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could lead to infection.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE PINK PERIPHERAL DYNDV1875 BOTTOM DRAWER ACC010972 DRAWER #4 ACC010479A DRAWER 2 ACC010690 ACC010875 DRAWER 3 SYR/DRS/MON/NG 1 OF 3 ACC011073…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0806-2026·2026-09-09
Baxter Recalls MYXREDLIN Insulin Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling MYXREDLIN insulin due to CGMP deviations. The recall covers specific lots distributed in the US, Puerto Rico, and Chile.
Product
MYXREDLIN — MYXREDLIN (INSULIN HUMAN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3056-2026·2026-09-09
Medline IV Start Kits Recalled for Potential Sterility Breach
Medline is recalling 22,736 IV start kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) IV START KIT LAB DRAW-SH, Model Number: CDS860014P; 2) IV START KIT, Model Number: DYKM1000B; 3) KIT, I V START NSK, Model Number: DYKM2187; 4) KIT, I V START NSK, Model Number: DYKM2187A; 5) IV BLOOD CULTURE KIT, Model Number: DYNDH1909A…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V579000·2026-09-09
Ford Recalls 2026-2027 Transit Vehicles for Rear Seat Belt Reminder Defect
Ford is recalling 2026-2027 Transit vehicles because the rear seat belt reminder system may malfunction, failing to alert occupants if a seat belt is unfastened.
Product
FORD — FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide