State

South Dakota product recalls

72,968 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 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5926–5950 of 75649

HighFDA (Devices)·Z-2119-2025·2025-07-23
NIO+ intraosseous device stabilizer may not release properly after insertion
The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.
Product
Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intraosseous access device supplied Sterile and single use. Indicated for Intraosseous access to t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2116-2025·2025-07-23
SwabCap disinfecting caps may have an incomplete seal allowing alcohol evaporation
SwabCap Disinfecting Caps for needlefree connectors are being recalled because an incomplete seal may let isopropyl alcohol evaporate, which may result in inadequate disinfection. 1,445,600 units affected.
Product
SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0523-2025·2025-07-23
Levothyroxine sodium 150 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 150 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,921 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0303-2025·2025-07-23
YoCrunch Snickers and Twix yogurt packages may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with Snickers and Twix pieces are being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Vanilla Yogurt with Snickers pieces (cup UPC 46675-00112), and 8-6oz (170g) cups of Vanilla Yogurt with Twix bar pieces (cup UPC 46675-00113). Two-Pack UPC 46675-02614. Keep Refrigerat
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2123-2025·2025-07-23
VITROS CHE slides sold in Japan can cause quality control drift
VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.
Product
VITROS Chemistry Products CHE Slides (Japan); Catalog Numbers: (1) 684 4074 (90 slides), (2) 684 4138 (300 slides);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2121-2025·2025-07-23
VITROS Performance Verifier II lots can cause quality control drift
VITROS Chemistry Products Performance Verifier II is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier II Model/Catalog Number: 8231474 Software Version: N/A Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2111-2025·2025-07-23
BLS DIODE laser projectors shipped without a working remote interlock connector
BLS laser light show projectors, models DIODE 1000, 2000 and 3000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 10 units affected.
Product
Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.
Category
Other
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0525-2025·2025-07-23
Omeprazole capsule bottle contained a foreign divalproex sodium tablet
Omeprazole Delayed-release Capsules USP 20 mg are being recalled because a foreign Divalproex Sodium Extended-Release 250 mg tablet was found in a bottle. 1,476 bottles affected.
Product
OMEPRAZOLE — OMEPRAZOLE (OMEPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0519-2025·2025-07-23
Levothyroxine sodium 25 microgram bottles of 1000 assayed below specification
Levothyroxine Sodium Tablets, USP 25 mcg in 1000-count bottles from Accord Healthcare are being recalled because the product is subpotent. 2,352 bottles are affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2125-2025·2025-07-23
EMPOWR 3D knee 10mm tibial inserts were packaged with wrong implant
EMPOWR 3D Knee Tibial Insert E-PLUS units, catalog number 341-10-711, are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units affected.
Product
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 10MM, VE Model/Catalog Number: 341-10-711 Software Version: NA Product Description: Enovis" knee devices are intended for treatment of patients who are candidates for knee arthroplasty p
Category
Medical Device
Distribution
18 states
HighFDA (Drugs)·D-0533-2025·2025-07-23
Rizatriptan 5 mg tablets exceed the acceptable intake limit for nitrosamine
Rizatriptan Benzoate Tablets USP 5 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0294-2025·2025-07-23
YoCrunch vanilla yogurt with M&M toppers may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, Packaged in the following size containers: 1. Single Serve Cup 6 oz (170g) UPC 46675-00079 2. Multipack consisting of 4-4 oz. cups UPC 46675-01351 Keep Refrigerated. Distributed by Danone US, White Plai
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0301-2025·2025-07-23
YoCrunch vanilla two-product yogurt packages may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with M&Ms and with Oreo pieces are being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Lowfat Yogurt with Toppers. Two-product packages. 1. Contains 8- 6oz (170g) cups of Vanilla Yogurt with milk chocolate M&Ms pieces (cup UPC 46675-00079), and 8-6oz (170g) cups of Vanilla Yogurt with Oreo pieces (cup UPC 46675-00080). Two-pack UPC 46675-01400.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0295-2025·2025-07-23
YoCrunch vanilla yogurt with Oreo pieces may contain plastic material
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Oreo cookie pieces, is being recalled because of foreign material in the form of plastic.
Product
YoCrunch Low Fat Yogurt with toppers. Vanilla with Oreo cookie pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00080 2. Multipack containing 4-4 oz. cups UPC 46675-01350 Keep Refrigerated. Distributed by Danone US, LLC, White
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0298-2025·2025-07-23
YoCrunch vanilla cookie dough yogurt multipacks may contain plastic pieces
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Chocolate Chip Cookie Dough pieces multipacks, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Chocolate Chip Cookie Dough pieces, Multipack containing 4-4 oz. (113g) cups. UPC 46675-01315. Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0296-2025·2025-07-23
YoCrunch vanilla yogurt with Snickers pieces may contain plastic pieces
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00112 2. Multipack containing 4-4 oz. cups UPC 46675-01326 Keep Refrigerated. Distributed by Danone US, LLC, White Pla
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0300-2025·2025-07-23
YoCrunch strawberry yogurt with M&M toppers may contain plastic pieces
YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis candies, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00083 2. Multipack containing 4-4 oz. cups UPC 46675-01312 Keep Refrigerated. Distributed by Dano
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0516-2025·2025-07-23
Lisdexamfetamine 60 mg capsules failed dissolution testing at nine month stability
Lisdexamfetamine Dimesylate Capsules 60 mg are being recalled because an out of specification result was observed in dissolution testing at the nine month long term stability station. 5,448 bottles affected.
Product
LISDEXAMFETAMINE DIMESYLATE — LISDEXAMFETAMINE DIMESYLATE (LISDEXAMFETAMINE DIMESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2114-2025·2025-07-23
NeuroSync EYE-SYNC headsets are inoperable and cannot be repaired
NeuroSync EYE-SYNC systems containing Pico Neo 2 headsets are being recalled because eye syncing issues render the device inoperable and it cannot be repaired. 27 units are affected.
Product
NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists of a Pico Neo 2 headset with embedded sensors, a paired Android tablet, and proprietary software, packaged in a portable field case. Eye-tracking headset system is intended for recording, viewing, and analyz
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0550-2025·2025-07-23
Power Stick roll-on antiperspirant recalled over manufacturing practice deviations
Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant is being recalled because of CGMP deviations. 23,467 cases are affected.
Product
Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz./ 53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-040-00 UPC Code 815195018224
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0548-2025·2025-07-23
Power Stick for her roll-on antiperspirant recalled over manufacturing deviations
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent is being recalled because of CGMP deviations. 21,265 cases are affected.
Product
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0549-2025·2025-07-23
Power Stick Spring Fresh roll-on antiperspirant recalled over manufacturing deviations
Beauty & Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant Spring Fresh is being recalled because of CGMP deviations. 22,482 cases are affected.
Product
Beauty & Skincare Power Stick original nourishing invisible protection roll-on Antiperspirant/Deodorant Spring Fresh, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-039-00, UPC Code 815195018194
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0273-2025·2025-07-23
New Mexico Pinon single serve coffee cup ink can run
New Mexico Pinon Coffee Dark Pinon Single Serve cups are being recalled because an inconsistent clear coat seal allows the food safe ink printing to run in a K-cup machine. 154 units affected.
Product
New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Number:F03308 UPC:812361033081. Single Serve (Keurig) Cups, filled with ground coffee flavored with natural flavorings.
Category
Food
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0517-2025·2025-07-23
Compounded testosterone pellet vials carry incorrect lot numbers from printing issue
Compounded Testosterone 200 mg Pellet in 1 mL amber vials is being recalled because a printing issue resulted in incorrect lot numbers on the label. 2,832 vials are affected.
Product
Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only, Compounded product. Qualgen 14844 Bristol Park Blvd Edmond OK 73013, NDC 69761-202-01
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V478000·2025-07-22
Winnebago airbag wiring can be caught in the seat mechanism
Winnebago is recalling certain 2024-2026 motorhomes because Supplemental Restraint System wires can be caught in the seat mechanism when the front seats are adjusted, damaging them.
Product
WINNEBAGO — WINNEBAGO REVEL, EKKO, NAVION, VIEW
Category
Vehicle
Distribution
Distributed nationwide