State

South Dakota product recalls

73,366 recalls have nationwide distribution and so reach South Dakota. 2,684 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total: 2,684
Critical: 401
Severe: 747
Most recent: 2026-09-23

Of the 2,684 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 2,684 recalls whose distribution notice names South Dakota specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18801–18825 of 76050

HighFDA (Food)·F-0093-2023·2022-11-09
Bella Cucina Artichoke Lemon Pesto Recalled for Undeclared Milk Allergen
Bella Cucina Artful Food is recalling Artichoke Lemon Pesto in three sizes because the label does not declare milk as an ingredient. The product was distributed to all U.S. states, Canada, and Italy.
Product
Bella Cucina Artful Food Artichoke Lemon Pesto Net Wt. 3.5 oz (100g) UPC 6 19193 00232 8, Net Wt. 17 oz (xxxg) UPC 6 19193 00132 1 & Net Wt. 23 oz (652g) UPC 6 1913 00130 7 in glass jar, Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0101-2023·2022-11-09
Bella Cucina Sun-Dried Tomato Pesto Recalled for Undeclared Milk Allergen
Bella Cucina Artful Food sun-dried tomato pesto is being recalled because the label does not indicate the presence of milk, a major allergen. Consumers with milk allergies are at risk.
Product
Bella Cucina Artful Food Sun-Dried Tomato Pesto Net Wt. 3 oz (84.5g) jar, UPC 6 19193 00213 7 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0167-2023·2022-11-09
NICU PICC Insertion Bundle Recalled for Breather Pouch Seal Defects
Medline Industries recalls NICU PICC insertion bundles (50 kits) due to openings in breather pouch seals that compromise sterile barrier integrity. This Class II recall affects units distributed across the United States.
Product
CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0024-2023·2022-11-09
Buprenorphine and Naloxone Sublingual Tablets Recalled for Foreign Substance
Sun Pharmaceutical is recalling buprenorphine and naloxone sublingual tablets (8 mg/2 mg) due to a foreign substance. Affected lots DNC1129A and DNC1740A were distributed nationwide.
Product
BUPRENORPHINE AND NALOXONE — BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0163-2023·2022-11-09
Medline LINQ Surgical Trays Recalled for Compromised Pouch Seals
Medline has recalled LINQ TRAY surgical kits with breather pouch seal openings that could compromise sterility. The recall affects 40 kits distributed nationwide; no injuries have been reported.
Product
MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0160-2023·2022-11-09
Surgical Cataract Kits Recalled for Defective Breather Pouch Seals
Medline has recalled Bausch + Lomb cataract surgical kits due to breather pouches with seal openings that could compromise sterility. Affected kits were distributed nationwide.
Product
BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0159-2023·2022-11-09
Surgical eye kits recalled for breached sterile pouches
Medline Industries recalls Bausch + Lomb eye muscle surgical kits due to breached breather pouches that may compromise sterility. The affected kits (Lot 22DBN366) were distributed nationwide.
Product
BAUSCH + LOMB EYE MUSCLE, REF VAL036EMESB. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0161-2023·2022-11-09
Surgical Cataract Packs with Compromised Breather Pouch Seals Recalled
Medline recalls 708 Bausch + Lomb cataract surgical packs due to breather pouch seal defects that could compromise sterility of surgical instruments.
Product
BAUSCH + LOMB CATARACT PACK, REF VAL001CPMEA. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0095-2023·2022-11-09
Bella Cucina Pastry Tarts Recalled for Undisclosed Milk Allergen
Bella Cucina Artful Food is recalling Crostata Sweet Butter Pastry Tarts because the label fails to indicate the presence of milk, a major allergen. Affected units were distributed across all U.S. states and internationally.
Product
Bella Cucina Artful Food CROSTATA SWEET BUTTER PASTRY TARTS Net Wt. 2.6 oz (73g) box, Distributed by Bella Cucina Artful Food Atlanta, GA 30310 UPC 6 19193 00721 7
Category
Food
Distribution
45 states
HighFDA (Food)·F-0104-2023·2022-11-09
Bella Cucina Sweet Pumpkin Pesto fails to declare milk allergen
Bella Cucina Sweet Pumpkin Pesto (6 oz jars, UPC 6 19193 00144 4) does not indicate milk on the label, posing a risk for consumers with milk allergies. The product was distributed across most US states, Canada, and Italy.
Product
Food Sweet Pumpkin Pesto Net Wt. 6 oz (169g) jar, UPC 6 19193 00144 4 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0097-2023·2022-11-09
Bella Cucina Dried Cherry and Almond Biscotti Recalled for Undeclared Milk and Wheat
Bella Cucina Artful Food is recalling Dried Cherry and Almond Biscotti because the label fails to indicate the presence of milk and wheat allergens. Consumers with allergies to these ingredients should not consume the product.
Product
Bella Cucina Artful Food Dried Cherry and Almond Biscotti Net Wt. 6 oz (170g) bag, UPC 6 19193 00019 5 Distributed by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0151-2023·2022-11-09
Boston Scientific EMBLEM S-ICD Subcutaneous Defibrillators Software Defect Causes Battery Display Error
Boston Scientific is recalling 7 EMBLEM S-ICD Model A209 subcutaneous defibrillators due to a software defect that displays inaccurate battery capacity information. Patients may not realize when their device's battery requires replacement.
Product
EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0099-2023·2022-11-09
Bella Cucina Porcini & Parmesan Pesto Recalled for Missing Milk Allergen Labeling
Bella Brands is recalling multiple lots of Bella Cucina Porcini & Parmesan Pesto because milk is not indicated on the product label, creating a risk for consumers with milk allergies.
Product
Bella Cucina Artful Food Porcini & Parmesan Pesto Net Wt. 6 oz (169g) jar, UPC 6 19193 00146 8 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0164-2023·2022-11-09
Medline Dental Pack Recall Due to Breather Pouch Seal Defect
Medline is recalling Dental Pack surgical kits (Lot 22DBE139) because breather pouches have openings in their seals that could compromise sterility. Affected units were distributed to healthcare facilities in eight US states.
Product
MEDLINE DENTAL PACK, REF DYNJ66983. Convenience kit used in medical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0102-2023·2022-11-09
Bella Cucina Sweet Pepper Pesto recalled due to undeclared milk allergen
Bella Cucina Artful Food Sweet Pepper Pesto is being recalled because the label does not declare milk as an ingredient. Consumers with milk allergies could experience a serious allergic reaction.
Product
Bella Cucina Artful Food Sweet Pepper Pesto Net Wt. 3 oz (84.5g) jar, UPC 6 19193 00233 5 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0155-2023·2022-11-09
Surgical Eye Kit Pouches Recalled for Seal Defects
Medline recalls Bausch + Lomb Eye surgical kits due to breather pouches with openings in the seal. Affected kits were distributed to healthcare facilities nationwide; unopened kits should not be used.
Product
BAUSCH + LOMB EYE PACK, REF LYN003EYSPA. Convenience kit used in surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0166-2023·2022-11-09
Medline CVC Barrier Kit Recalled for Breached Pouch Seals
Medline is recalling CVC barrier kits (Lot 22ABT774) due to breather pouches with seal openings that could compromise sterility of the surgical kit contents.
Product
MEDLINE CVC BARRIER KIT, REF DYNJ80485. Convenience kit used in medical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0165-2023·2022-11-09
Medline Radiology Procedure Pack Breather Pouches Recalled for Seal Defects
Medline is recalling 240 Radiology Procedure Packs because some breather pouches show seal openings that could compromise sterility. The affected kits were distributed nationwide.
Product
MEDLINE RADIOLOGY PROCEDURE PACK, REF DYNJ67150A. Convenience kit used in medical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0152-2023·2022-11-09
Implantable Defibrillator Software Error Causes Inaccurate Battery Display
Boston Scientific's EMBLEM MRI S-ICD implantable defibrillators contain a software defect with an incorrect manufacturing date that causes inaccurate battery capacity display. The recall affects 142 devices distributed worldwide.
Product
EMBLEM MRI S-ICD, Subcutaneous Implantable Defibrillator, Model A219, sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0162-2023·2022-11-09
Medline Lithotomy Sterile Surgical Kit Recalled for Compromised Breather Pouch Seal
Medline is recalling 96 sterile surgical kits (REF DYNJ50099C, Lot 22DBL482) distributed nationwide due to complaints of openings in breather pouches that compromise sterility and increase contamination risk.
Product
MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0105-2023·2022-11-09
Bella Cucina Pizza Mix Recalled for Undeclared Wheat Allergen
Bella Cucina Tradizionale Pizza and Foccacia Mix is being recalled because the label does not declare wheat, a common allergen. Consumers with wheat allergies could experience allergic reactions.
Product
Bella Cucina Artful Food Tradizionale Pizza and Foccacia Mix Net Wt. 15 oz 422g can, Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0098-2023·2022-11-09
Bella Cucina Fresh Basil Pesto Recalled for Undisclosed Milk Allergen
Bella Cucina Artful Food is recalling Fresh Basil Pesto because the label does not disclose milk. The product may cause allergic reactions in consumers with milk allergies.
Product
Bella Cucina Artful Food Fresh Basil Pesto Net Wt. 3 oz (84.5g) bag, UPC 6 19193 00211 3 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Food)·F-0100-2023·2022-11-09
Bella Cucina Spinach Artichoke Bruschetta Spread Recalled for Undisclosed Milk
Bella Cucina Artful Food is recalling Spinach Artichoke Bruschetta Spread because the label does not indicate milk. Consumers with milk allergies should not consume this product.
Product
Bella Cucina Artful Food Spinach Artichoke Bruschetta Spread Net Wt. 10 oz (286g) jar, UPC 6 19193 00501 5 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-0147-2023·2022-11-09
Fogarty Biliary Balloon Probes recalled for latex deterioration
Edwards Lifesciences is recalling Fogarty Biliary Balloon Probes due to confirmed latex deterioration in pouches. The recall affects 26,560 units distributed worldwide.
Product
Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0168-2023·2022-11-09
Pediatric Vision Scanner Battery Pack Poses Fire Risk
Rebiscan is recalling Blinq Pediatric Vision Scanners (Model BQ830) because the battery pack may vent and catch fire if a cell voltage drops below 2.5V.
Product
Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for automated detection of misalignment of the visual axes using polarized light. Model Number BQ830
Category
Medical Device
Distribution
Distributed nationwide