The Recall Desk

State

District of Columbia product recalls

72,982 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 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6476–6500 of 75777

  • HighFDA (Devices)·Z-1894-2025·2025-06-11

    Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled

    Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.

    Product
    Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2025·2025-06-11

    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.

    Product
    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0455-2025·2025-06-11

    Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination

    Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2025·2025-06-11

    MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect

    Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.

    Product
    MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0458-2025·2025-06-11

    Hand Sanitizer Recalled for Subpotent Ethyl Alcohol Content

    Spectrum Advanced Gel Hand Sanitizer (70% ethyl alcohol, 8 FL OZ) has been recalled nationwide because affected batches contain cloudy appearance and test below the claimed 70% alcohol concentration, making them less effective.

    Product
    HAND SANITIZER — HAND SANITIZER (ETHYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0457-2025·2025-06-11

    Lacosamide Oral Solution recalled for defective leaking containers

    Apotex Corp. is recalling Lacosamide Oral Solution because certain bottles may leak when stored horizontally. Patients taking this seizure medication should contact their pharmacy or healthcare provider.

    Product
    Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0454-2025·2025-06-11

    Indomethacin Extended-Release Capsules recalled for cGMP deviations

    Amerisource Health Services LLC is recalling Indomethacin Extended-Release Capsules 75 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects 21 cartons distributed nationwide.

    Product
    INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1913-2025·2025-06-11

    DxI 9000 Access Immunoassay Analyzer Software Update Error Codes

    Beckman Coulter is recalling DxI 9000 Access Immunoassay Analyzers running software version 1.20 because the update introduces error codes that prevent assays from being performed and may delay result generation.

    Product
    DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1907-2025·2025-06-11

    Beckman Coulter Sample Probe Manufacturing Defect Recall

    Beckman Coulter Mishima is recalling sample probes due to a manufacturing defect where rounded and chamfered corners prevent proper air layer formation, causing sample dilution and inaccurate test results.

    Product
    Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1891-2025·2025-06-11

    FoundationOne Companion Diagnostic F1CDx Incorrect Claim Display

    Foundation Medicine is recalling the FoundationOne Companion Diagnostic (F1CDx) due to an incorrect negative claim displayed on the claims page, though device variant information was correctly shown in the tumor profiling section of the approved test report.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1909-2025·2025-06-11

    Pre-filled Water Syringe recalled for improper use contamination

    Healthmark Industries is recalling Pre-filled Water Syringes (Model SW-010-100 and SW-010) after duodenoscope contamination was linked to improper use of the syringes outside their intended purpose.

    Product
    Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1890-2025·2025-06-11

    FoundationOne Companion Diagnostic contains incorrect negative claims

    Foundation Medicine is recalling two FoundationOne Companion Diagnostic (F1CDx) test reports that contained an incorrect negative claim on the claims page, though the device variant information displayed correctly in the tumor profiling section.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V364000·2025-06-10

    Forest River trailer side gate latches may unlock during transit

    Forest River is recalling certain 2025 Salem and Wildwood travel trailers because the side entry gate latch may unlock, allowing the strut to open the gate during transit.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V331000·2025-06-10

    Hyundai Translead Recalls 2026 Dry Van Trailers for Liftgate Pin Defect

    Hyundai Translead is recalling 2026 Dry Van Trailers because insufficient lubrication on the liftgate cylinder pin may cause it to seize, leading to liftgate failure and injury risk.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DRY VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V381000·2025-06-09

    Braun Recalls 1,533 Vehicles for Loose Seat Belt Fasteners

    Braun is recalling 1,533 Chrysler Pacifica, Voyager, and Toyota Sienna vehicles because seat belt tie-down fasteners may be loose, increasing injury risk in crashes.

    Product
    BRAUN — BRAUN CHRYSLER VOYAGER, CHRYSLER PACIFICA, TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V332000·2025-06-06

    Volvo Recalls 2025-2026 VN Trucks for Power Cable Routing Defect

    Volvo Trucks North America is recalling 2025-2026 Volvo VN trucks because improperly routed power cables may cause electrical shorts, leading to engine stalls or fires.

    Product
    VOLVO — VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V375000·2025-06-06

    2018–2024 Harley-Davidson Softail motorcycles rear shock issue

    Harley-Davidson is recalling certain 2018–2024 Softail motorcycles because the rear shock pre-load adjuster mounting tab may break and damage the tire, causing sudden loss of pressure and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FLHCS ANV, FXLRS, FXLRST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V379000·2025-06-06

    Mercedes-Benz GLC 300 and AMG GLC models roof impact protection

    Mercedes-Benz is recalling certain 2023–2025 GLC 300 and GLC 300 4MATIC, 2024–2025 AMG GLC 43 4MATIC, 2025 GLC 350E 4MATIC, and 2025 AMG GLC 63 S E vehicles with panoramic sunroofs. The C-pillar may not absorb adequate impact in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E 4MATIC, GLC 300 4MATIC, AMG GLC63 S E, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·25316·2025-06-05

    Portable Hook-On Chairs Recalled for Fall Hazard and Serious Injury Risk

    Portable hook-on chairs sold on Amazon by Ravmix pose a fall hazard because the crotch restraint can be removed without tools, allowing infants to fall through. The product violates federal safety standards. Consumers should stop using immediately and contact Ravmix for refund instructions.

    Product
    Portable Hook-On Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25311·2025-06-05

    BowFlex Adjustable Dumbbells Recalled Due to Dislodging Weight Plates

    About 3.8 million BowFlex 552 and 1090 adjustable dumbbells are recalled because weight plates can dislodge from the handle during use. Over 100 injuries have been reported, including concussions and broken toes.

    Product
    BowFlex 552, 52.5 LB Adjustable Dumbbells and BowFlex 1090, 90 LB Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25322·2025-06-05

    Apollo America Combination Smoke and Carbon Monoxide Detectors Recalled

    Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.

    Product
    Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V378000·2025-06-05

    Honda CR-V Hybrid fuel feed hose may be improperly installed

    Honda is recalling certain 2025 CR-V Hybrid vehicles because the fuel feed hose may have been improperly installed, allowing fuel to leak. This fails FMVSS 301.

    Product
    HONDA — HONDA CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25315·2025-06-05

    ZHORANGE Portable Bassinets Recalled for Fall Hazard Risk

    ZHORANGE portable bassinets (model 148012-A) are recalled due to sides that are too low and absence of a stand, creating a fall hazard for infants. The product violates federal safety standards for infant sleep products.

    Product
    ZHORANGE Portable Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide