The Recall Desk

State

District of Columbia product recalls

73,218 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
948
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 948 (34%) are Severe.

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14826–14850 of 76016

  • HighCPSC·23271·2023-08-31

    Prime-Line Recalls Glass Doorknobs Due to Laceration Hazard

    Prime-Line glass doorknobs can crack and separate, creating a laceration hazard. The firm has received five reports of injuries requiring stitches.

    Product
    Glass Doorknobs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23787·2023-08-31

    Chemboys DIYChemicals Potassium and Sodium Hydroxide Lacks Child-Resistant Packaging

    Chemboys is recalling DIYChemicals potassium hydroxide and sodium hydroxide products because the packaging is not child-resistant and labels lack mandatory hazard information. The products pose a risk of chemical burns and eye irritation to children.

    Product
    DIYChemicals: Potassium Hydroxide/KOH Flakes and Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23786·2023-08-31

    Ski-Doo and Lynx Snowmobiles Recalled for Fire Hazard

    Bombardier Recreational Products is recalling about 4,070 model year 2023 Ski-Doo and Lynx snowmobiles equipped with 850 E-TEC Turbo R engines because the main injector fuel return hose can leak, posing a fire hazard.

    Product
    Ski-Doo and Lynx Snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23270·2023-08-31

    Apollo Phantom Electric Scooters Recalled for Fall and Injury Hazards

    Apollo Imports Inc. is recalling approximately 3,900 Apollo Phantom Electric Scooters because a stem bolt can come loose, causing the suspension and wheel assembly to separate and posing a fall and injury hazard. The company has received seven reports of bolt breaking, including three injuries.

    Product
    Apollo Phantom Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V607000·2023-08-31

    Nova Bus LFS Transit Buses Electrical Short Circuit Fire Risk

    Nova Bus is recalling 2017–2023 LFS and LFS Artic transit buses due to a potential electrical short circuit in the 24-volt power cable and fuse holder assembly that may cause overheating and fire risk while driving or parked.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V609000·2023-08-31

    2022 Subaru BRZ vehicles recalled for inoperative rear turn signals

    Subaru is recalling certain 2022 BRZ and Toyota GR86 vehicles because the rear turn signals may intermittently stop working. Inoperative signals increase the risk of a crash by failing to notify other drivers of a turning vehicle.

    Product
    SUBARU — SUBARU, TOYOTA BRZ, GR86
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V610000·2023-08-31

    Kia 2022–2023 Sorento Hybrid rearview camera mounting clips may break

    Kia is recalling certain 2022–2023 Sorento, Sorento Hybrid, and Sorento PHEV vehicles because the rearview camera mounting clips may break, preventing the camera image from displaying properly and reducing rear visibility.

    Product
    KIA — KIA SORENTO HYBRID, SORENTO, SORENTO PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23272·2023-08-31

    Boon Flair and Flair Elite Highchairs Recalled for Fall Hazard

    TOMY International is recalling about 83,000 Boon Flair and Flair Elite highchairs because loose bolts can allow the seat to detach from the base, creating a fall hazard. The company has received 34 reports of separation, including 24 falls with 11 injuries.

    Product
    Boon Flair & Flair Elite highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23E065000·2023-08-31

    GM Recalls Webasto Portable Charging Cords Due to Grounding Defect

    General Motors is recalling specific Webasto portable charging cords that may fail to stop charging if the ground connection is lost, posing an electric shock risk.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1479-2023·2023-08-30

    Soft Serve on the Go Ice Cream Recalled Due to Listeria Contamination

    Real Kosher Ice Cream's Soft Serve on the Go Caramel Vanilla ice cream (8 fl oz) may be contaminated with Listeria monocytogenes. The product was distributed across multiple US states and internationally.

    Product
    Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz; UPC 0-91404-15131-3
    Category
    Food
    Distribution
    20 states
  • SevereNHTSA·23V606000·2023-08-30

    Micro Bird Recalls G5 Transit Buses Due to Seat Detachment Risk

    Micro Bird is recalling 2018-2019 and 2021 G5 transit buses because seats over the fuel filler may detach, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1481-2023·2023-08-30

    Soft Zero on the Go Lite Peanut Butter Ice Cream Recalled for Listeria

    Soft Zero on the Go brand Lite Peanut Butter ice cream is being recalled due to potential Listeria monocytogenes contamination. The affected product was distributed across multiple U.S. states and internationally.

    Product
    Soft Zero on the Go brand Lite Peanut Butter flavor; 8 fl oz; UPC 0-91404-15285-3
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1477-2023·2023-08-30

    Soft Serve on the Go Vanilla Chocolate Ice Cream Recalled for Listeria

    Real Kosher Ice Cream, Inc. is recalling Soft Serve on the Go brand Vanilla Chocolate ice cream due to potential Listeria monocytogenes contamination. The product was distributed across multiple U.S. states and several countries.

    Product
    Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15129-0 Soft Serve on the Go brand Parve Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15113-9
    Category
    Food
    Distribution
    20 states
  • SevereNHTSA·23V604000·2023-08-30

    Volkswagen Recalls 2019-2020 Models for Ignition Switch Failure Risk

    Volkswagen is recalling specific 2019-2020 models because the ignition switch may fail, causing the engine to stall while driving and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF SPORTWAGEN, GTI, JETTA, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2023·2023-08-30

    Carina Sub-Acute Care Ventilator Recalled for Toxic Chemical Emission

    Draeger Medical is recalling 11,621 Carina Sub-Acute Care Ventilators because polyurethane components emit 1,3-Dichloropropan-2-ol at levels exceeding safe limits during extended use in pediatric patients.

    Product
    Carina Sub-Acute Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1480-2023·2023-08-30

    Soft Serve on the Go Strawberry Mango Sorbet Recalled for Listeria Contamination Risk

    Real Kosher Ice Cream, Inc. is recalling Soft Serve on the Go brand Strawberry Mango Sorbet due to potential Listeria monocytogenes contamination. The product was distributed across multiple U.S. states and international locations.

    Product
    Soft Serve on the Go brand Sorbet Strawberry Mango Sorbet flavor; 8 fl oz; UPC 0-91404-15128-3
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1478-2023·2023-08-30

    Soft Serve on the Go Peanut Butter ice cream recalled for Listeria contamination

    Real Kosher Ice Cream recalls Soft Serve on the Go Peanut Butter ice cream due to potential Listeria contamination. Consumers should discard the product or return it.

    Product
    Soft Serve on the Go brand Razzle n' Dazzle Peanut Butter flavor; 8 fl oz; UPC 0-91404-15133-7
    Category
    Food
    Distribution
    20 states
  • HighNHTSA·23V603000·2023-08-30

    Interstate Recalls 2023 ITLT716A2 Trailers Due to Pinch Hazard

    Interstate is recalling 2023 ITLT716A2 trailers because steel tie-down straps may interfere with the deck tilt latch, creating a pinch point that increases the risk of injury.

    Product
    INTERSTATE — INTERSTATE ITLT716A2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2462-2023·2023-08-30

    Medicrea IMPIX MANTA+ Cervical Fusion Devices Recalled for Packaging Defect

    Medicrea International is recalling IMPIX MANTA+ cervical intervertebral fusion devices due to potential packaging non-conformity with pinholes in inner or outer pouches. No illnesses or injuries reported.

    Product
    IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20171963, h) B20171973, i) B20172253, j) B20172263, k) B20172273; intervertebral fusion device - cervical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2459-2023·2023-08-30

    Medicrea GRANVIA-C Cervical Fusion Device Recalled for Packaging Defects

    Medicrea International is recalling GRANVIA-C cervical intervertebral fusion devices due to a packaging non-conformity issue presenting as pinholes in inner or outer pouches, which could compromise sterility.

    Product
    GRANVIA-C, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567, c)¿¿¿¿¿ A13113456, d)¿¿¿¿ A13131516, e)¿¿¿¿ A13131789, f)¿¿¿¿¿¿ A13132012, g)¿¿¿¿¿ B13111014, h)¿¿¿¿ B13111015, i)¿¿¿¿¿¿ B13111016, j)¿¿¿¿¿¿ B13111017, k)¿¿¿¿¿ B13111025, l)¿¿¿¿¿¿ B13111026…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2445-2023·2023-08-30

    Dolomite Gloss Rollator Structural Failure Recall: Seat Collapse Risk

    Dolomite Gloss Rollator models may experience seat failure and structural collapse due to broken eyelets and crossbar, potentially causing user injury. About 586 units nationwide are affected.

    Product
    DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat. Model Number(s): 1654807 - DOLOMITE GLOSS 680 ROLLATOR 1655081 - DOLOMITE GLOSS 600 ROLLATOR 1655082 - DOLOMITE GLOSS 520 ROLLATOR 1655083 - DOLOMITE GLOSS 450 ROLLATOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2456-2023·2023-08-30

    Intervertebral fusion device recalled for packaging non-conformity issue

    Medicrea International is recalling 4,489 IMPIX MANTA intervertebral fusion devices due to potential pinholes in product packaging that could compromise device sterility.

    Product
    IMPIX MANTA, REF numbers: a) A20150407, b) A20250407, c) A20350567, d) B20181743, e) B20181753, f) B20181763, g) B20181773, h) B20181943, i) B20181953, j) B20181963, k) B20181973, l) B20182253, m) B20182263; intervertebral fusion device - lumbar
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2447-2023·2023-08-30

    Air/Water Valve Used with Olympus Endoscopes May Malfunction

    Olympus air/water valves used with ultrasonic endoscopes may fail during automated reprocessing, potentially allowing body fluids to backflow into the air channel. Approximately 29,590 units nationwide are affected.

    Product
    The Air/Water Valve is provided/used with the following Endoscopes: ULTRASONIC GASTROFIBERSCOPE, ULTRASONIC GASTROVIDEOSCOPE, ULTRASONIC COLONOVIDEOSCOPE: GF-UC140P-AL5, GF-UCT140-AL5, GF-UE160-AL5, GF-UCT180, GF-UM20, GF-UM130, GF-UMQ130, GF-UM160, GF-UC160P-OL5…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1457-2023·2023-08-30

    Butter Flavored Popcorn recalled for undeclared milk

    Bickel's Snack Foods Inc is recalling Butter Flavored Popcorn because the product contains undeclared milk. The recall affects approximately 6,048 bags distributed in Georgia and nationwide retail stores.

    Product
    Butter Flavored Popcorn Naturally & Artificially Flavored, 8oz. UPC: 70175 06021 Packaged in clear plastic bags, 9 bags per case.
    Category
    Food
    Distribution
    Distributed nationwide