State

South Dakota product recalls

72,907 recalls have nationwide distribution and so reach South Dakota. 2,681 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total: 2,681
Critical: 401
Severe: 565
Most recent: 2026-09-02

Of the 2,681 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 565 (21%) are Severe.

Which agencies issued them

These figures cover only the 2,681 recalls whose distribution notice names South Dakota specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1001–1025 of 75588

SevereFDA (Food)·H-1101-2026·2026-07-01
Spring & Mulberry Mulberry Fennel Chocolate Bars Recalled for Salmonella
Spring & Mulberry Inc. is recalling Mulberry Fennel Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recalled product was distributed nationwide.
Product
Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a burgundy box, UPC 850055470149, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0623-2026·2026-07-01
ChloraPrep One-Step Topical Solution Sterility Assurance Recall
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) due to wrinkles in the paper lidding that may breach the seal, compromising sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1103-2026·2026-07-01
Spring & Mulberry Date-Sweetened Chocolate Recalled for Salmonella
Spring & Mulberry Inc. is recalling Pure Dark and Pure Dark Minis date-sweetened chocolate products nationwide due to potential Salmonella contamination. Consumers should not consume the affected products and should discard or return them.
Product
1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a navy blue box, UPC 850055470002, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1098-2026·2026-07-01
Spring & Mulberry Earl Grey Date-Sweetened Chocolate Bars Recalled
Spring & Mulberry Inc. is recalling Earl Grey Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.
Product
Spring & Mulberry Earl Grey Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470231, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indivi
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1099-2026·2026-07-01
Spring & Mulberry Lavender Rose Chocolate Recalled for Salmonella
Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.
Product
Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0625-2026·2026-07-01
ChloraPrep One-Step Antiseptic Solution Recall Due to Sterility Concerns
CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1096-2026·2026-07-01
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate Recalled Due to Salmonella
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate bars are recalled due to potential Salmonella contamination. The product was distributed nationwide.
Product
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail produc
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1106-2026·2026-07-01
Spring & Mulberry Blood Orange Date-Sweetened Chocolate recalled for Salmonella
Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.
Product
Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold in
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1104-2026·2026-07-01
Spring & Mulberry Sea Salt Date-Sweetened Chocolate recalled for Salmonella
Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.
Product
Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individua
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2586-2026·2026-07-01
Medline Industries Polycarbonate Syringes Convenience Kits Design Change Recall
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. Affected kits were distributed nationwide and internationally.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIOGRAPHY PACK-LF DYNJ0854485S DEEP BRAIN STIMULATION PACK DYNJ0842793G NEURO ACCESSORY PACK DYNJ55385A NEURO ANGIO PACK DYNJ51697B DYNJ56509G DYNJ56509I DYNJ680
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2571-2026·2026-07-01
Surgify Halo surgical burrs recalled for potential breakage during spinal surgery
Surgify Medical OY is recalling Surgify Halo 5.4 mm Long surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The defect could affect patient safety during the procedure.
Product
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2559-2026·2026-07-01
Surgify Halo spinal surgery burr tool potential breakage recall
Surgify Halo 4.0 mm extendable surgical burrs may break during bi-portal endoscopic spinal surgery. The device is being recalled to prevent patient injury from burr fragments.
Product
Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2560-2026·2026-07-01
Surgify Halo surgical burr recalled for potential breakage risk
Surgify Medical is recalling the Surgify Halo 4.0 mm surgical burr because it may break during bi-portal endoscopic spinal surgery. The device is distributed nationwide.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2573-2026·2026-07-01
Surgify Halo Surgical Burr May Break During Spinal Surgery
Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The recalled burrs have UDI 06429811532335 and were distributed nationwide.
Product
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1095-2026·2026-07-01
Motor City Pizza Co. 5 Cheese Bread recalled for salmonella risk
Champion Foods, LLC is recalling Motor City Pizza Co. 5 Cheese Bread due to potential salmonella contamination. Affected products were distributed nationwide at major retailers.
Product
Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC 8 70375 00511 1; 6 retail units per case Motor City Pizza Co. 5 Cheese Bread Twin retail pack; 44.86 oz. (2 lb. 12.9 oz.) 1272g UPC 8 70375 00509 8; 10 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2565-2026·2026-07-01
Surgify Halo Surgical Burr Recalling Potential Tool Breakage Risk
SURGIFY MEDICAL OY is recalling the Surgify Halo 5.4 mm Extendable surgical burr due to risk of burr breakage during bi-portal endoscopic spinal surgery (BESS). The recalled units are distributed nationwide.
Product
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0628-2026·2026-07-01
Perampanel Prescription Tablets Recalled for Labeling Mix-up
Sun Pharmaceutical is recalling Perampanel 6 mg tablets due to labeling mix-up where 10 mg tablets were found in bottles labeled as 6 mg. Patients should verify their bottles with their pharmacy or physician.
Product
PERAMPANEL — PERAMPANEL (PERAMPANEL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2532-2026·2026-07-01
Acumed Hexalob Screws Recalled for Risk of Fracture During Use
Acumed LLC is recalling Hexalob Screws of various sizes used with wrist fixation systems due to a manufacturing error that may cause the screws to break during use.
Product
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL Hexalobe Screw; 3070-27010 2.7mm x 10mm NL Hexalobe Screw; 3070-27011 2.7mm x 11mm NL Hexalobe Screw; 3070-27012 2.7mm x 12mm NL Hexalobe Screw; 3070-27013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2580-2026·2026-07-01
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall
Boston Scientific Corporation is recalling the Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump (model AP-0300H) due to potential leakage along the drug pathway from the pump through the catheter.
Product
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2567-2026·2026-07-01
Surgify Halo surgical burrs recalled for potential breakage
Surgify Halo 5.4 mm Short surgical burrs may break during bi-portal endoscopic spinal surgery. FDA Class II recall affects multiple U.S. states.
Product
Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2561-2026·2026-07-01
Surgify Halo 4.0 mm Spinal Surgery Burrs May Break During Use
Surgify Halo 4.0 mm Short burrs may break during bi-portal endoscopic spinal surgery, creating a potential hazard during the procedure. The FDA has classified this as a Class II recall affecting devices nationwide.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2528-2026·2026-07-01
Zimmer Shoulder Reamer Guide System Recalled for Plastic Breakage
Zimmer is recalling Off-Axis Comprehensive Shoulder System reamer guides (Model 110040241) because plastic guides can catch and break during reaming. Five complaints have been received.
Product
Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0626-2026·2026-07-01
Lacosamide 100mg Tablets Recalled Due to Foreign Tablet Contamination
Annora Pharma is recalling Lacosamide 100mg tablets nationwide after discovering Selexipag 1000 mcg tablets mixed into bottles. Patients taking the wrong medication could experience unintended health effects.
Product
LACOSAMIDE — LACOSAMIDE (LACOSAMIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2562-2026·2026-07-01
Surgify Halo surgical drill may break during spinal surgery procedures
Surgify Halo 4.0 mm surgical drills are being recalled because the burr may break during bi-portal endoscopic spinal surgery. The defect could interfere with the surgical procedure.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2568-2026·2026-07-01
Surgify Halo Surgical Burr Breakage Risk During Spinal Surgery
Surgify Medical is recalling Surgify Halo 5.4 mm Medium surgical burrs due to potential burr breakage during bi-portal endoscopic spinal surgery. The device poses a risk of fragmentation that could complicate surgical procedures.
Product
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide