The Recall Desk

State

District of Columbia product recalls

72,971 recalls have nationwide distribution and so reach DC. 2,795 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total
2,795
Critical
240
Severe
946
Most recent
2026-09-02

Of the 2,795 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 946 (34%) are Severe.

These figures cover only the 2,795 recalls whose distribution notice names District of Columbia specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5926–5950 of 75766

  • SevereCPSC·25389·2025-07-17

    CasaClean handheld steamers can leak steam or spew hot boiling water

    CasaClean Handheld Steamers, model DF-958, are being recalled because they can leak steam or spew hot boiling water. Thirteen consumers have received burns. About 23,000 units are affected.

    Product
    CasaClean Handheld Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25390·2025-07-17

    iStore magnetic wireless power banks can overheat and ignite while charging

    iStore Magnetic Wireless Power Banks, model IST-09991/W05, are being recalled because the lithium-ion battery can overheat and ignite while charging. Three incidents and about $15,000 in property damage reported.

    Product
    iStore Magnetic Wireless Power Banks (IST-09991/W05 model only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25387·2025-07-17

    Traveller aluminum loading ramps can bend or break under rated loads

    Traveller aluminum loading ramps are being recalled because they cannot withstand the weight specified on the ramps and can bend or break in use. Two injuries have been reported. About 18,000 units affected.

    Product
    Traveller Aluminum Loading Ramps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2025·2025-07-17

    Kayem Foods Recalls Chicken Sausage Due to Plastic Contamination

    Kayem Foods is recalling ready-to-eat chicken sausage products nationwide due to possible contamination with pieces of plastic.

    Product
    Kayem Foods Inc. — Kayem Foods Inc. Recalls Ready-To-Eat Chicken Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V473000·2025-07-17

    Grand Design trailer entrance door latch mechanism may fail

    Grand Design is recalling certain 2025-2026 Lineage trailers with Lippert Modularia entrance doors because the door latch mechanism may fail, potentially trapping occupants in an emergency.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V471000·2025-07-17

    Chrysler Pacifica built with wrong radio may not show rearview image

    Chrysler is recalling certain 2024-2025 Pacifica vehicles that were built with an incorrect radio, which can prevent the rearview camera image displaying. All affected vehicles have been repaired.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25392·2025-07-17

    Babyletto Kiwi recliner USB modules can overheat and spark in use

    Babyletto Kiwi Electronic Recliner and Swivel Gliders are being recalled because the USB module in the recliner arm can overheat and spark. About 9,030 units are affected.

    Product
    Babyletto Kiwi Electronic Recliner and Swivel Gliders with USB port
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25388·2025-07-17

    Primark Stitch scented highlighters contain phthalates above the federal ban

    Primark DTR Stitch Scented Highlighters 4-packs are being recalled because they contain phthalates in violation of the federal phthalates ban. About 2,600 units are affected.

    Product
    Primark DTR (direct-to-retail) Stitch Scented Highlighters (4-pack)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V474000·2025-07-17

    Genesis G90 and GV60 instrument panel display can fail

    Hyundai is recalling certain 2023-2025 Genesis G90 and GV60 vehicles because a software error may cause the instrument panel display to fail, failing FMVSS 101.

    Product
    GENESIS — GENESIS GV60, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V472000·2025-07-17

    Jeep Grand Cherokee second-row head restraints may not lock upright

    Chrysler is recalling certain 2023-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because the second-row head restraints may not lock in the upright position, failing FMVSS 202.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E044000·2025-07-17

    Chrysler Recalls Mopar Second-Row Head Restraints for Locking Defect

    Chrysler is recalling Mopar second-row head restraints that may not lock in the upright position, increasing injury risk during a crash.

    Product
    SEATS:MID/REAR ASSEMBLY:HEAD RESTRAINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2083-2025·2025-07-16

    FEM-FLEX II femoral arterial cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0213-2025·2025-07-16

    JLM dark chocolate nonpareils recalled over undeclared milk allergen

    JLM Manufacturing Dark Chocolate Nonpareils in 14 oz tubs are being recalled because of undeclared milk. 971 cases are affected, distributed nationwide.

    Product
    JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2047-2025·2025-07-16

    Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction

    The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.

    Product
    Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2084-2025·2025-07-16

    FEM-FLEX II FEMII018A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2082-2025·2025-07-16

    FEM-FLEX II FEMII016A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII016A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 6,801 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2085-2025·2025-07-16

    FEM-FLEX II FEMII018AS cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018AS, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 558 units affected.

    Product
    Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS Software Version: N/A Product Description: The Edwards FEMFLEXII Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2080-2025·2025-07-16

    Optisite OPTI16 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI16 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 27,022 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V470000·2025-07-16

    BMW electric vehicle battery modules may be improperly assembled

    BMW is recalling certain 2022-2025 iX, 2023-2024 i7 and 2022-2023 i4 vehicles because high-voltage battery cell modules may not have been assembled properly, stressing the module frame.

    Product
    BMW — BMW I4, I7, IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0220-2025·2025-07-16

    Wegmans chocolate chip mini muffins may contain foreign objects of metal

    Wegmans brand Chocolate Chip Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.

    Product
    Wegmans brand Mini Muffins; CHOCOLATE CHIP; NET WT 13.5 OZ; packaged in plastic clamshell; UPC 7789053223
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2101-2025·2025-07-16

    O-arm O2 imaging system gantry support may have been damaged

    The O-arm O2 Imaging System is being recalled because a mechanical component supporting the gantry to the support structure may have been damaged during manufacture. 3 units affected.

    Product
    O-arm O2 Imaging System. Mobile X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2025·2025-07-16

    VersaCross access kits may have a hole in the sterile pouch

    VersaCross Access Solution kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.

    Product
    VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF WIRE 63CM/45DEG/D1) VXSK0102 VXSK (180J RF WIRE 63CM/55DEG/D0) VXSK0103 VXSK (180P RF WIRE 63CM/45DEG/D0) VXSK0121 VXSK (180P RF WIRE 63CM/45DEG/D1)
    Category
    Medical Device
    Distribution
    Distributed nationwide