The Recall Desk

State

District of Columbia product recalls

73,596 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total
2,798
Critical
240
Severe
1,083
Most recent
2026-09-23

Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,083 (39%) are Severe.

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1751–1775 of 76394

  • ModerateFDA (Devices)·Z-2581-2026·2026-07-01

    Medline Polycarbonate Syringes Recalled for Unapproved Design Changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA-cleared specifications. Affected kits were distributed nationwide.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIOGRAM PACK-LF DYNJ21574J JUDKINS PACK DYNJ51126
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2596-2026·2026-07-01

    Medline 10mL Polycarbonate Syringes Recalled for Unapproved Design Changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The affected kits were distributed nationwide.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. FTMC C-SECTION TRAY-LF DYNJ54603B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2584-2026·2026-07-01

    Medline 10mL Polycarbonate Colored Syringes Convenience Kits Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes because the products underwent unapproved design changes outside of FDA clearance.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR G'S BREAST PACK DYNJ51124B LIPO SUPPLEMENT PACK-LF DYNJ0341174D PLASTIC PACK DYNJ66746 DYNJ85702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0617-2026·2026-07-01

    Duloxetine 30 mg capsules recalled for impurity above FDA limits

    Direct Rx is recalling Duloxetine D/R 30 mg capsules (also sold as Cymbalta) distributed nationwide because the drug contains N-nitroso-duloxetine impurity above FDA-recommended interim limits.

    Product
    DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60), 60 Caps; CYMBALTA, Packaged and Distributed by Direct Rx.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0611-2026·2026-07-01

    Fenofibrate Capsules 200 mg Recalled for CGMP Manufacturing Deviations

    Ajanta Pharma USA Inc. is recalling Fenofibrate Capsules, USP 200 mg due to Current Good Manufacturing Practice (CGMP) deviations identified during production. The recall affects 3,648 bottles distributed nationwide.

    Product
    FENOFIBRATE — FENOFIBRATE (FENOFIBRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2576-2026·2026-07-01

    Octopus Evolution AS Tissue Stabilizer Model TS2500 Tubing Assembly Issue Recall

    Medtronic is recalling 288 units of the Octopus Evolution AS Tissue Stabilizer Model TS2500 due to incorrect tubing positioning during manufacturing, where short and long tubes were attached to wrong locations.

    Product
    Octopus Evolution AS Tissue Stabilizer, Model TS2500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0614-2026·2026-07-01

    Sensipar Cinacalcet Tablets Recalled Due to CGMP Deviations

    Amgen, Inc. is recalling Sensipar (cinacalcet) 60 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects 30-count bottles with Lot #1157055 and expiration date 1/31/2028.

    Product
    SENSIPAR — SENSIPAR (CINACALCET HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2575-2026·2026-07-01

    Octopus Evolution Tissue Stabilizer Model TS2000 tubing assembly error

    Medtronic Perfusion Systems is recalling the Octopus Evolution Tissue Stabilizer, Model TS2000, due to an assembly error where tubing was incorrectly positioned during manufacturing.

    Product
    Octopus Evolution Tissue Stabilizer, Model TS2000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0619-2026·2026-07-01

    Hydroxyzine Hydrochloride Oral Solution recalled for foreign substance

    ANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution due to the presence of a foreign substance. The affected lot is S25133A, distributed nationwide.

    Product
    HYDROXYZINE HYDROCHLORIDE — HYDROXYZINE HYDROCHLORIDE (HYDROXYZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V417000·2026-06-30

    Ford Recalls 2021-2023 Mustang Mach E for Rear Differential Defect

    Ford is recalling 2021-2023 Mustang Mach E vehicles because the rear differential pinion shaft may fracture, potentially causing loss of drive power or unintended movement.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V413000·2026-06-30

    Chrysler Recalls Jeep Models Due to Missing Gear Indicator Software Error

    Chrysler is recalling specific 2022-2024 Jeep models because a software error may cause the transmission gear selection indicator to fail to display.

    Product
    JEEP — JEEP GRAND CHEROKEE L, WAGONEER, GRAND CHEROKEE, WAGONEER L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V414000·2026-06-30

    Chrysler Recalls 2026 Jeep Grand Wagoneer Models for Brake Software Defect

    Chrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles because brake software may disable stability control and brake assist, increasing crash risk.

    Product
    JEEP — JEEP GRAND WAGONEER, GRAND WAGONEER L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V418000·2026-06-30

    2025 Ford Mustang windshield wiper and washer system failure recall

    Ford is recalling certain 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because the windshield wipers may function only at high speed and the washing system may fail during cold temperatures, reducing visibility and increasing crash risk.

    Product
    FORD — FORD MUSTANG, MUSTANG GTD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V419000·2026-06-30

    2026 Nissan Rogue Transmission Gear Indicator Display Failure

    Nissan is recalling certain 2026 Rogue vehicles because the instrument panel may not display the transmission gear selection indicator, potentially leading to unintended vehicle movement or rollaway.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V416000·2026-06-30

    Jayco Recalls 2027 Motorhomes Due to Missing Dinette Brackets

    Jayco is recalling 2027 Entegra Accolade and Seneca motorhomes because missing front brackets allow the dinette to shift, increasing injury risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V420000·2026-06-30

    Teko Recalls 2026 Electric Vehicles for Missing Pedestrian Warning System

    Teko is recalling 2026 Triumph, Trophy, Trophy Plus, Turbo, and TurboLite vehicles because the acoustic vehicle alerting system may be missing, increasing pedestrian crash risk.

    Product
    TEKO — TEKO TURBOLITE, TURBO, TROPHY PLUS, TROPHY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E039000·2026-06-30

    Nissan Recalls JATCO Transaxles for Gear Indicator Display Failure

    Nissan is recalling specific JATCO automatic transmission assemblies because a hardware failure may cause the gear shifter indicator to display incorrectly, increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:GEAR POSITION INDICATION (PRNDL) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V412000·2026-06-29

    Tiffin Motorhomes Recreational Vehicles Rooftop Fan Fire Risk Recall

    Tiffin Motorhomes is recalling certain 2026–2027 recreational vehicles with MaxxAir N-Series Maxxfan rooftop ventilation fans. The circuit board may overheat and increase the risk of fire.

    Product
    TIFFIN — TIFFIN MIDAS, WAYFARER, OPEN TRAIL, ALLEGRO OPEN ROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V411000·2026-06-29

    Jayco Recalls 2024 Alante and Vision RVs for Incorrect Weight Labels

    Jayco is recalling 2024 Alante and Entegra Vision recreational vehicles because the occupant and cargo capacity labels may list incorrect weights, potentially leading to vehicle overloading.

    Product
    JAYCO — JAYCO, ENTEGRA ALANTE, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V410000·2026-06-26

    Nissan Recalls 2025 Sentra Vehicles for Driveshaft Defect

    Nissan is recalling 2025 Sentra vehicles because a front left driveshaft may not be fully seated, risking transmission fluid leaks and loss of drive power.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V408000·2026-06-26

    Thomas Built Buses Recalls SAF-T-LINER HDX2 Due to Door Malfunction

    Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 buses because the entrance door may fail to open or close, increasing injury risk in crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V407000·2026-06-26

    Thomas Built School Bus Recall for Door Switch Failure

    Daimler Trucks is recalling 2026-2027 Thomas Built school buses because the entrance door may fail to open or close, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide