State

South Dakota product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

401–425 of 76262

CriticalFDA (Food)·H-1396-2026·2026-09-30
Bettergoods Lemon Alfredo Fettuccine Recalled for Listeria Contamination
GIAS FOOD INC. is recalling Bettergoods Lemon Alfredo Fettuccine due to Listeria monocytogenes contamination. Consumers should stop eating the product and return it to Walmart.
Product
Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0862-2026·2026-09-30
Sterling Recalls Carboxymethylcellulose Sodium Eye Drops Due to Sterility Concerns
Sterling Pharmaceutical Services LLC is recalling specific lots of Cameron Pharmaceuticals Carboxymethylcellulose Sodium 0.5% Eye Lubricant due to a lack of assurance of sterility.
Product
Lubricant Eye Drops-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3139-2026·2026-09-30
CooperSurgical Recalls Infant Nasal CPAP Tubing Due to Loose Connection Risk
CooperSurgical is recalling specific lots of INCA Infant Nasal CPAP tubing because a loose connection may cause loss of pressure and reduced oxygenation.
Product
INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-2707, 44-2709, 44-2710, 44-2712, 44-2715.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0858-2026·2026-09-30
Walgreens Lubricant Eye Drops Recalled for Sterility Assurance Concerns
Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. The recall affects 199,600 packs distributed nationwide.
Product
WALGREENS LUBRICANT EYE DROPS — WALGREENS LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V628000·2026-09-30
Grech Motorhomes Recalled for Rooftop Fan Fire Risk
Grech is recalling 2026-2027 Strada, Terreno, and Turismo motorhomes because a rooftop ventilation fan circuit board may overheat and cause a fire.
Product
GRECH — GRECH TURISMO, STRADA, TERRENO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V627000·2026-09-30
Highland Ridge Range Lite Air Travel Trailer Fresh Water Tank Recall
Highland Ridge RV is recalling 2022-2024 Range Lite Air travel trailers because fastener failure may cause the fresh water tank to detach, creating a road hazard.
Product
HIGHLAND RIDGE TT — HIGHLAND RIDGE TT RANGE LITE AIR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0856-2026·2026-09-30
Sodium Chloride Ophthalmic Solution Recalled for Sterility Assurance Issues
Sterling Pharmaceutical Services is recalling Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, due to a lack of assurance of sterility.
Product
SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% — SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% (SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5%)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0859-2026·2026-09-30
Sterling Pharmaceutical Recalls Lubricating Tears Due to Sterility Concerns
Sterling Pharmaceutical Services LLC is recalling specific lots of Lubricating Tears because the company cannot guarantee the product is sterile.
Product
LUBRICATING TEARS — LUBRICATING TEARS (CARBOXYMETHYLCELLULOSE SODIUM 0.5% SOLUTION)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0860-2026·2026-09-30
Gentle Eyes Lubricant Eye Drops Recalled for Sterility Concerns
Sterling Pharmaceutical Services LLC is recalling Gentle Eyes Lubricant Eye Drops due to a lack of assurance of sterility.
Product
GENTLE EYES LUBRICANT EYE DROPS — GENTLE EYES LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0861-2026·2026-09-30
Sterling Recalls Major LubriFresh P.M. Ointment for Sterility Concerns
Sterling Pharmaceutical Services LLC is recalling Major LubriFresh P.M. Nighttime Ointment due to a lack of assurance of sterility. The recall covers 34,368 tubes distributed nationwide.
Product
Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0863-2026·2026-09-30
AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution due to a lack of assurance of sterility.
Product
CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3266-2026·2026-09-30
Medline Neurological Sponges Recalled for Potential Endotoxin Variability
Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.
Product
Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DYNJ81325A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3244-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recall Due to Ceramic Tip Detachment Risk
Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Product
Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0855-2026·2026-09-30
AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns
Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% due to a lack of assurance of sterility.
Product
CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0870-2026·2026-09-30
Clear Eyes Redness Relief Eye Drops Recalled for Sterility Concerns
Insight Pharmaceuticals is recalling 2.3 million bottles of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.
Product
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0871-2026·2026-09-30
Clear Eyes Redness Relief Eye Drops Recalled for Sterility Assurance Issues
Insight Pharmaceuticals is recalling specific lots of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.
Product
Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0857-2026·2026-09-30
Walgreens Lubricant Eye Drops Recalled for Lack of Sterility Assurance
Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. Consumers should stop using the product.
Product
WALGREENS LUBRICANT EYE DROPS — WALGREENS LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3214-2026·2026-09-30
Boston Scientific Recalls Imager II Angiographic Catheters Due to Tip Fracture Risk
Boston Scientific is recalling Imager II Angiographic Catheters because the tip may fracture or detach, potentially causing device fragments to remain in or migrate through the patient's vasculature.
Product
Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5; M001314011 IMAGER II/5/ST/100/038 BX5; M001314021 IMAGER II/5/ST/65/035 BX 5; M001314031 IMAGER II/5/ST/100/035 BX 5; M001314041 IMAGER II/5/BARNH/100/038 BX5; M001314051 IMAGER…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3140-2026·2026-09-30
CooperSurgical Recalls Neonatal Nasal CPAP Replacement Sets Due to Loose Tubing
CooperSurgical is recalling 149 boxes of INCA Neonatal Nasal CPAP replacement sets because the flexible tubing may disconnect from the nasal cannula, potentially reducing treatment effectiveness.
Product
INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-0712, 44-0707, 44-0709, 44-0715.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3229-2026·2026-09-30
Medline Instrument Channel Brush Kits Recalled for Sharp Edges
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.
Product
Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3245-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recalled for Ceramic Tip Detachment Risk
Olympus is recalling 105 BiCOAG Hemostasis Probes because a manufacturing defect may cause the ceramic tip to detach during use.
Product
Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector. Model/Catalog Number: CD-B612LA.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3247-2026·2026-09-30
Olympus BiCOAG Hemostasis Probe Recalled for Potential Ceramic Tip Detachment
Olympus Corporation of the Americas is recalling 816 units of BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Product
Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3249-2026·2026-09-30
Philips EPIQ Elite Ultrasound System Recalled for Software Error
Philips is recalling 219 EPIQ Elite Diagnostic Ultrasound Systems due to a software issue that may cause inaccurate blood flow velocity measurements and potential misdiagnosis.
Product
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3250-2026·2026-09-30
Becton, Dickinson ForeSight Elite Tissue Oximetry Cable Recall for Incorrect Channel Switching
Becton, Dickinson and Company is recalling 15,455 ForeSight Elite Tissue Oximetry Cables due to incorrect switching of Channel 1 and 2 on the module and flag labels.
Product
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter cable is intended for use as an adjunct monitor of absolute regional hemoglobin oxygen saturation of blood under the sensors in individuals at risk for reduced…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3215-2026·2026-09-30
Heidelberg SPECTRALIS Flex Module Recall Due to Wheel Detachment Risk
Heidelberg Engineering is recalling 87 SPECTRALIS units with Flex Modules because wheels may detach, causing the stand to tip over and injure nearby people.
Product
Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module Model/Catalog Number: S3610, S2610, S2000, S1610 multimodal imaging platform optimized for the posterior segment of the eye
Category
Medical Device
Distribution
Distributed nationwide