State

South Dakota product recalls

72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2601–2625 of 75600

HighFDA (Devices)·Z-1643-2026·2026-04-01
Olympus PKS cutting forceps 920000PK jaws may break from welds
Olympus is recalling PKS Cutting Forceps with cord, model 920000PK, because a supplier did not adequately validate the welding process and defective welds can cause the jaw to break.
Product
Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1642-2026·2026-04-01
Olympus PKS cutting forceps 3005PK jaws may break from defective welds
Olympus is recalling PKS Cutting Forceps model 3005PK because a supplier did not adequately validate the welding process and defective welds can cause the jaw to break during clinical use.
Product
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualiza
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1610-2026·2026-04-01
Olympus endoscope suction valve no longer compatible with named reprocessors
Olympus is recalling the MAJ-1443 Endoscope Suction Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Product
Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0405-2026·2026-04-01
Teva octreotide acetate 20 mg recalled over sterility assurance deficiencies
Teva is recalling nine lots of Octreotide Acetate for Injectable Suspension 20 mg after quality system deficiencies were identified during an FDA inspection at the contract manufacturer.
Product
OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1603-2026·2026-04-01
I.T.S. femur and tibia plates heat more in MRI than stated
I.T.S. GmbH is recalling the LRS Locking Reconstruction System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corresponding article numbers. 1. DFL (Distal Femur Locking) Distal Femur Plate; Article Numbers: 21301-5, 21301-7, 21301-9, 21301-13, 21302-5, 21302-7, 21302-9, 21302-13. 2. PTL (Proximal Lateral
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0406-2026·2026-04-01
Teva octreotide acetate injection recalled over sterility assurance deficiencies
Teva is recalling twelve lots of Octreotide Acetate for Injectable Suspension after quality system deficiencies were identified during an FDA inspection at the contract manufacturer.
Product
OCTREOTIDE ACETATE — OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2026·2026-04-01
I.T.S. volar radius plates heat more in MRI than stated
I.T.S. GmbH is recalling Volar Radius Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1640-2026·2026-04-01
Olympus PK cutting forceps jaws may break from defective welds
Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation dur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1638-2026·2026-04-01
Olympus Everest bipolar forceps model 3005 jaws may break
Olympus is recalling Everest Bipolar Cutting Forceps model 3005 because a supplier did not adequately validate the welding process, and defective welds can cause the jaw to break during clinical use.
Product
Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3005 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved u
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V207000·2026-04-01
Mack Recalls 2025-2027 Trailers Due to Turn Signal Software Defect
Mack Trucks is recalling 2025-2027 Pioneer and 2027 Anthem trailers because turn signals may not function properly, increasing crash risk.
Product
MACK — MACK PIONEER PR (4), ANTHEM AN (4)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1599-2026·2026-04-01
I.T.S. cannulated screw system heats more in MRI than stated
I.T.S. GmbH is recalling the I.T.S. Screw System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
I.T.S. Screw System with the below descriptions and corresponding article numbers. 1. Cancellous Screw, Cannulated; Article Numbers: 31404-16, 31404-18, 31404-20, 31404-22, 31404-24, 31404-26, 31404-28, 31404-30, 31404-32, 31404-34, 31404-36, 31404-38, 31404-40, 31404-42, 314
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1613-2026·2026-04-01
Olympus OER-Pro reprocessor no longer compatible with two valve models
Olympus is recalling the OER-Pro Endoscope Reprocessor because the MAJ-1443 and MAJ-1444 air/water valves are no longer reprocessing compatible with the OER-Pro and OER-Elite reprocessors.
Product
Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1632-2026·2026-04-01
Straumann custom abutments made from wrong bar material after mix-up
Straumann is recalling Custom Abutment Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.
Product
Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1609-2026·2026-04-01
Beckman Coulter MicroScan gram-negative panels may contain contaminated wells
Beckman Coulter is recalling one lot of MicroScan Neg MIC 56 panels due to the likely presence of contamination in one or more wells.
Product
MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V209000·2026-04-01
Audi Q3 recalled over remote sunroof closing from out of sight
Volkswagen Group of America is recalling 6,077 Audi Q3 vehicles because incorrect software may allow remote sunroof closing from a distance where the operator cannot clearly see the sunroof.
Product
AUDI — AUDI Q3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2026·2026-04-01
I.T.S. clavicle plates heat more in MRI than instructions state
I.T.S. GmbH is recalling Clavicula Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10. 2. Clavicle Plate; Article Numbers: 21121-6, 21121-8. 3. Clavicle Plate, 3.5mm; Article
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2026·2026-04-01
I.T.S. calcaneus repair plate heats more in MRI than stated
I.T.S. GmbH is recalling the FR.O.H. Calcaneus Repair System anterolateral calcaneus plate because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1597-2026·2026-04-01
I.T.S. olecranon plates heat more in MRI than instructions state
I.T.S. GmbH is recalling Olecranon Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Olecranonplate with Angular Stability with the below descriptions and corresponding article numbers. 1. Olecranon Hook Plate; Article Numbers: 21112-7, 21114-5, 21113-9. 2. Olecranon Plate; Article Numbers: 21111-6, 21111-8, 21111-12.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1602-2026·2026-04-01
I.T.S. distal humeral plates heat more in MRI than stated
I.T.S. GmbH is recalling Distal Humeral Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers. 1. Cortical Screw, Locking; Article Numbers: 37351-10-N, 37351-12-N, 37351-14-N, 37351-16-N, 37351-18-N, 37351-20-N, 37351-22-N, 37351-24-N, 37351-26-N, 37351-28-N, 373
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0590-2026·2026-04-01
Chilli Spanish Peanuts Recalled for Glass Contamination Risk
Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bags, Lot #260230) due to glass fragments found in sealed containers.
Product
Chilli Spanish Peanuts, Treasured Harvest brand, 25lb clear plastic bag container. UPC:none Item code: 2608-25
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0615-2026·2026-04-01
Savannah Bee Company Honey BBQ Sauce Mustard Undeclared Allergens
Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.
Product
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED VINEGAR, WATER, MUSTARD SEED, SALT, SPICES (INCLUDING PAPRIKA AND TUMERIC), NATURAL FLAVOR, GARLIC), HONEY, WATER, DISTILLED VINEGAR, SUGAR, TOMATO CONCENTRATE, HA
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-1639-2026·2026-04-01
Olympus Everest bipolar cutting forceps jaws may break from defective welds
Olympus is recalling Everest Bipolar Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1633-2026·2026-04-01
Straumann angled custom abutments made from wrong bar material
Straumann is recalling Custom Abutment AS Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.
Product
Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0589-2026·2026-04-01
Chilli Spanish Peanuts First Street recalled for glass contamination
Western Mixers Produce & Nuts, Inc. is recalling First Street Chilli Spanish Peanuts (11 oz) because glass fragments were found in sealed containers. Affected lots have expiration dates of 2/11/2027, 2/13/2027, and 2/23/2027.
Product
Chilli Spanish Peanuts, First Street brand, 11oz clear plastic container. UPC: None Item Code: 2608-T20
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1611-2026·2026-04-01
Olympus endoscope air water valves no longer compatible with named reprocessors
Olympus is recalling the MAJ-1444 Endoscope Air/Water Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Product
Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
Category
Medical Device
Distribution
Distributed nationwide