State

West Virginia product recalls

72,968 recalls have nationwide distribution and so reach West Virginia. 3,541 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total: 3,541
Critical: 593
Severe: 657
Most recent: 2026-09-09

Of the 3,541 recalls naming West Virginia we have scored against our rubric, 593 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 657 (19%) are Severe.

Which agencies issued them

These figures cover only the 3,541 recalls whose distribution notice names West Virginia specifically. The 72,968 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5901–5925 of 76509

HighFDA (Food)·H-0297-2025·2025-07-23
YoCrunch vanilla yogurt with Twix pieces may contain plastic pieces
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00113 2. Multipack containing 4-4 oz. cups UPC 46675-01327 Keep Refrigerated. Distributed by Danone US, LLC, White Plai
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0520-2025·2025-07-23
Levothyroxine sodium 50 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
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 (Drugs)·D-0522-2025·2025-07-23
Levothyroxine sodium 112 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 112 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,896 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0304-2025·2025-07-23
YoCrunch strawberry and raspberry granola yogurt may contain plastic pieces
A YoCrunch Lowfat Yogurt with Toppers two-product package containing strawberry and raspberry yogurt with granola is 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 Strawberry Yogurt with Granola pieces (Cup UPC 46675-00010), and 8-6oz (170g) cups of Raspberry Yogurt with Granola pieces (Cup UPC 46675-01401). Two- Pack, UPC 46675-01401. Keep Refrige
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 (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 (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 (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 (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-0521-2025·2025-07-23
Levothyroxine sodium 100 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 100 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 9,739 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0299-2025·2025-07-23
YoCrunch strawberry granola yogurt cups may contain plastic foreign material
YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces in 6 oz single serve cups, is being recalled because of foreign material in the form of plastic pieces.
Product
YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces, Single Serve Cup, 6 oz. (170g) UPC 46675-00010. Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
Category
Food
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 (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-2118-2025·2025-07-23
NIO-A intraosseous device stabilizer may not release properly after insertion
The NIO-A 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. 7,056 US units affected.
Product
Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2112-2025·2025-07-23
BLS laser show projectors shipped without a working remote interlock connector
BLS laser light show projectors, models CLUB 1000, 2000 and 4000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 12 units affected.
Product
Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
Category
Other
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 (Drugs)·D-0532-2025·2025-07-23
Lisinopril and hydrochlorothiazide bottle contained a foreign antiretroviral tablet
Lisinopril and Hydrochlorothiazide Tablets 20 mg/12.5 mg are being recalled after a complaint that a sealed bottle contained a foreign tablet identified as atazanavir and ritonavir. 58,968 bottles affected.
Product
LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2113-2025·2025-07-23
BLS PURE laser projectors shipped without a working remote interlock connector
BLS laser light show projectors, models PURE 5000 and PURE 10000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 3 units affected.
Product
Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
Category
Other
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0524-2025·2025-07-23
Levothyroxine sodium 175 microgram tablets assayed below the approved specification
Levothyroxine Sodium Tablets, USP 175 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 2,344 bottles affected.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0302-2025·2025-07-23
YoCrunch strawberry two-product yogurt packages may contain plastic pieces
YoCrunch Lowfat Yogurt with Toppers two-product packages containing strawberry 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 package. Contains 8-6oz (170g) cups of Strawberry Yogurt with milk chocolate M&Ms pieces (cup UPC 46675-00084), and 8-6oz (170g) cups of Strawberry Yogurt with Oreo pieces (cup UPC46675-00083). Two-Pack UPC 46675-02613. Kee
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2025·2025-07-23
VITROS CHE slides can cause quality control drift with performance verifiers
VITROS Chemistry Products CHE Slides 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; Catalog Numbers: (1) 191 4605 (300 slides), (2) 800 4707 (90 slides);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2120-2025·2025-07-23
VITROS Performance Verifier I lots can cause quality control drift
VITROS Chemistry Products Performance Verifier I 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 I Model/Catalog Number: 806 7324 Software Version: Not Applicable Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor perfo
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0534-2025·2025-07-23
Rizatriptan 10 mg tablets exceed the acceptable intake limit for nitrosamine
Rizatriptan Benzoate Tablets USP 10 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