State

South Dakota product recalls

73,596 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: 399
Severe: 749
Most recent: 2026-10-14

Of the 2,686 recalls naming South Dakota we have scored against our rubric, 399 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 749 (28%) are Severe.

Which agencies issued them

These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28251–28275 of 76282

ModerateFDA (Devices)·Z-3027-2020·2020-10-07
Greiner Bio-One Recalls VACUETTE Blood Collection Tubes Due to Separation Issues
Greiner Bio-One is recalling VACUETTE blood collection tubes because they experienced an issue with separation and clotting.
Product
VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect, transport, and process blood for testing serum, plasma or whole blood in the clinical laboratory.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3033-2020·2020-10-07
Ameditech Recalls Consult Diagnostics Drugs Abuse Test Cups
Ameditech Inc is recalling 31,600 units of Consult Diagnostics Drugs Abuse Test Cups because immunoassay enzymes failed performance tests, leading to inconsistent detection of compounds.
Product
Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Description): 164-DXA14 /"Consult Diagnostics DRUGS OF ABUSE TEST CUP 14-DRUG PANEL WITH ADULTERANTS AMP500/BAR/BUPG/BZO/COC150/MDMA/MET500/MOP/MTD/OXY/PCP/PPX/TCA/THC (Bl, Cr, Ni, pH, SG)",
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0003-2021·2020-10-07
Teva Recalls Buprenorphine Transdermal Patches for Stability Failures
Teva Pharmaceuticals USA is recalling Buprenorphine Transdermal Systems because they failed stability specifications for release rate.
Product
BUPRENORPHINE — BUPRENORPHINE (BUPRENORPHINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3035-2020·2020-10-07
Ameditech Recalls One Step + DOA Cup Due to Performance Failures
Ameditech is recalling 31,800 units of the Henry Schein One Step + DOA Cup because the immunoassay enzymes failed performance tests, resulting in inconsistent detection of compounds.
Product
Henry Schein One Step + DOA Cup (AMT Item Number/ AMT Description): 570-1066 / "Henry Schein OneStep+ DOA Cup 14 Panel AMP500/BAR/BUPG/BZO/COC150/MDMA/MET500/MOP/MTD/OXY/PCP/PPX/TCA/THC (Bl, Cr, Ni, pH, SG)",
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1628-2020·2020-10-07
Akorn Recalls Eye Itch Relief Eye Drops Due to Manufacturing Deviations
Akorn, Inc. is voluntarily recalling 25,843 bottles of Eye Itch Relief eye drops due to CGMP deviations. The product was distributed nationwide in 14 states.
Product
Eye Itch Relief, Ketotifen Fumarate Ophthalmic Solution 0.035%, Sterile, 5 mL, Distributed by CVS Pharmacy, Inc. Woonsocket, RI 02895, NDC 59779-920-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3029-2020·2020-10-07
Ameditech Recalls Alere iScreen Single Drug Detection Dip Cards
Ameditech is recalling Alere iScreen Single Drug Detection dip cards because they may fail to consistently detect certain compounds at labeled levels.
Product
Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description): X11-IS1 BUP-DX/ "Alere iScreen" Dx Single Dip Card Single Drug Detection: Buprenorphine (BUP)", X11-IS1 BAR-DX /"Alere iScreen" Dx Single Dip Card Single Drug Detection: Barbiturate (BAR)", X11-IS1…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3051-2020·2020-10-07
Ameditech Drug Screening Components Recalled for Performance Failures
Ameditech Inc is recalling specific drug screening components because they failed to consistently detect compounds at labeled levels.
Product
Drug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number 100163/ EDI OPI (300) Uncut Sheet-Card /187876, 100195/ EDI PPX Uncut Sheet-Card/ 187877, 160130/ EDI COC Uncut Sheet-Cup/ 188168, 160180/ EDI PCP Uncut Sheet-Cup/ 189027, 160140/ EDI THC Uncut…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3016-2020·2020-10-07
Cardinal Health Pre-Op Decolonization Kit Recall for Missing Nasal Swabs
Cardinal Health is recalling pre-operative decolonization kits that contain only one nasal swab instead of the four required for proper treatment.
Product
KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3048-2020·2020-10-07
Ameditech Recalls First Check 2 Panel Drug Cups Due to Performance Failures
Ameditech is recalling 41,340 units of First Check 2 Panel Drug Cups because the products failed to consistently detect compounds at labeled levels.
Product
First Check 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0001-2021·2020-10-07
Strides Recalls Potassium Chloride Tablets for Failed Dissolution Specifications
Strides Inc. is recalling 11,280 bottles of Potassium Chloride Extended-Release Tablets because they failed to meet dissolution specifications.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1627-2020·2020-10-07
pH-D Boric Acid Vaginal Suppositories Recalled for Lack of FDA Approval
pH-D Feminine Health is recalling Boric Acid Vaginal Suppositories because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
pH-D Feminine Health Boric Acid Vaginal Suppositories, 24 vaginal suppositories per box, 600 mg each, pH-D Feminine Health, LLC Madison, TN 37115, UPC Code: 3 49597 00044 5.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3031-2020·2020-10-07
Ameditech Recalls Alere iCup Drug Detection Cups Due to Performance Failures
Ameditech Inc is recalling Alere iCup Drug Detection cups because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.
Product
Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/ "Alere" iCup¿ Dx 10 Drug Detection + Adulteration AMP/BAR/BZO/COC/MET/MDMA/MTD/MOP/OXY/THC Bl, Cr, Ni, pH, SG", I-DXA-13B/"Alere" iCup¿ DX Drug Screen Cup 13 Drug Detection + Adulteration…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3034-2020·2020-10-07
Ameditech Fastect II Drug Screen Dipstick Tests Recalled for Performance Failures
Ameditech is recalling Fastect II Drug Screen Dipstick Tests because they failed to consistently detect compounds at labeled levels.
Product
Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Item Number/ AMT Description): MF25/ "Fastect¿ II Drug Screen Dipstick Test Single Drug Detection: BUP10", QF09/"Fastect¿ II Drug Screen Dipstick Test, 4 Drug Detection: THC50+COC300+OPI300+BZO300", MF20…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3044-2020·2020-10-07
Ameditech Recalls TDDA Drugs of Abuse Cups Due to Performance Failures
Ameditech Inc is recalling TDDA Drugs of Abuse Cups because the immunoassay enzymes failed to consistently detect all compounds at labeled levels.
Product
TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA Drugs of Abuse Cup AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G."
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3028-2020·2020-10-07
Beckman Coulter Recalls UIBC Reagent Lot 2690 Due to Erroneous Results
Beckman Coulter is recalling 219 units of UIBC reagent lot 2690 because it produces erroneously high patient results at the low end of the linear range.
Product
UIBC; Catalog Number: OSR61205; UDI (01) 15099590011925; IVD; Rx Only; WARNING H316 H317 H351 H373 H411 - Product Usage: System reagent for the quantitative determination of Unsaturated Iron Binding Capacity (UIBC) in human serum and plasma on Beckman Coulter AU analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3040-2020·2020-10-07
Ameditech iCup Dx14 Drug Screen Cup Recalled for Performance Failures
Ameditech is recalling iCup Dx14 Drug Screen Cups because immunoassay enzymes failed performance tests, causing inconsistent detection of compounds.
Product
iCup Dx14 Drug Screen Cup(AMT Item Number/ AMT Description): X11-I-DXA-2147-011/ "iCup" Dx 14 Drug Screen Cup 14 Drug Detection: (THC50/COC150)+(MOP300/MET500)+(AMP500/BZO300)+ (BAR300/MTD300)+(BUPG10/TCA1000)+(MDMA500/OXY100)+(PCP25/PPX300) 5 Adulteration Tests: Cr, Ni…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3047-2020·2020-10-07
Ameditech Recalls First Check 14 Panel Drug Cups Due to Performance Failures
Ameditech is recalling 47,005 units of First Check 14 Panel Drug Cups because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.
Product
First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1625-2020·2020-10-07
Arbor Pharmaceuticals Recalls Subpotent Nymalize Oral Solution
Arbor Pharmaceuticals is voluntarily recalling Nymalize (nimodipine) oral solution because the drug is subpotent. The FDA classifies this as a Class III recall.
Product
Nymalize (nimodipine) oral solution, 60 mg/20 mL, 12 Unit-Dose Cups and 12 Oral Syringes, 2 inner cartons per outer shipping carton, Rx Only, Distributed by arbor Atlanta, GA, NDC 24338-200-12
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V614000·2020-10-06
Ferrari Recalls 812 Superfast Vehicles for Rear Window Adhesion Defect
Ferrari is recalling 2018-2020 812 Superfast vehicles because the rear window may have been bonded incorrectly, potentially leading to detachment and increased crash risk.
Product
FERRARI — FERRARI 812 SUPERFAST
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V615000·2020-10-06
Motorhome propane stove gas leak recall affects 2020-2021 models
REV is recalling certain 2020-2021 Fleetwood and Holiday Rambler motorhomes with Dometic propane stoves due to potential gas leaks that could increase fire risk. Owners should contact REV for free repair at 1-800-509-3417.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD ADMIRAL, FLAIR, BOUNDER, SOUTHWIND
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E075000·2020-10-06
TriMark Recalls 50-200 Door Latches for Emergency Vehicles
TriMark is recalling 50-200 door latches used in emergency vehicles because trip levers may fail, preventing doors from opening.
Product
LATCHES/LOCKS/LINKAGES:DOORS:LATCH recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E074000·2020-10-06
Lippert Components Recalls Electric Motors in Power Bedlift Systems
Lippert Components is recalling electric motors in Power Bedlift systems because internal gear failure may cause the bed to extend unexpectedly, increasing injury risk.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V617000·2020-10-06
Vespa GTS 300 and GTV 300 Scooters Recalled for Brake Pipe Defect
Piaggio is recalling 2020-2021 Vespa GTS 300 and GTV 300 scooters because improperly galvanized brake pipe terminals can reduce braking efficiency and increase crash risk.
Product
VESPA — VESPA GTV 300, GTS 300
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V616000·2020-10-06
REV Recalls 2019 Road Rescue Type I Ambulances for Door Latch Defect
REV Ambulance Group is recalling 2019 Road Rescue Type I ambulances because incorrect material in door latches may prevent doors from opening, creating a lock-in risk.
Product
ROAD RESCUE — ROAD RESCUE TYPE I
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V611000·2020-10-05
Yamaha Recalls YZF-R3, XMAX, and MT-03 Models for Rear Reflector Defect
Yamaha is recalling specific 2015-2020 motorcycles and scooters because condensation on the rear reflector lens may reduce its effectiveness, increasing crash risk.
Product
YAMAHA — YAMAHA YZF-R3, XMAX, redundant YZF-R3, MT-03
Category
Vehicle
Distribution
Distributed nationwide