The Recall Desk

State

Washington product recalls

72,984 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,456
Critical
867
Severe
2,006
Most recent
2026-09-09

Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.

These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6226–6250 of 81440

  • 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-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-2126-2025·2025-07-23

    EMPOWR 3D knee tibial inserts were packaged with the wrong implant

    EMPOWR 3D Knee Tibial Insert E-PLUS units are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units are affected.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 12MM, VE Model/Catalog Number: 341-12-711 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-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 (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-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 (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 (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-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 (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-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 (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 (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
  • HighNHTSA·25V482000·2025-07-23

    Hyundai IONIQ 5 battery bus bar may be improperly tightened

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the high voltage battery may contain an improperly tightened bus bar that can short circuit. Owners are told to park outside until repaired.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    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-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 (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-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