The Recall Desk

State

District of Columbia product recalls

73,576 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.

Which agencies issued them

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

501–525 of 76374

  • CriticalFDA (Devices)·Z-3127-2026·2026-09-23

    Medline Recalls Blood and Urine Collection Kits Due to Fungal Contamination

    Medline is recalling 47,848 blood and urine collection kits nationwide because they may contain Aspergillus penicillioides, a fungus that can cause serious infection.

    Product
    Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number: DYNDB3100; 3) DYNDH1619A, Catalog Number: DYNDH1619A; 4) DYNDH1620A, Catalog Number: DYNDH1620A; 5) DYNDH1694A, Catalog Number: DYNDH1694A; 6) DYNDH1695, Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3128-2026·2026-09-23

    Nova StatStrip Glucose Hospital Meter System Recalled for Software Defect

    Nova Biomedical is recalling StatStrip Glucose Hospital Meter Systems due to a software defect that may cause patient glucose results to be assigned to the wrong medical record.

    Product
    StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0866-2026·2026-09-23

    Vitruvias Recalls Superpotent Thyroid Tablets Nationwide

    Vitruvias Therapeutics is voluntarily recalling 1,955 bottles of Thyroid Tablets due to superpotency. The FDA classifies this as a Class I recall.

    Product
    THYROID — THYROID (THYROID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3126-2026·2026-09-23

    Medline Convenience Kits Recalled for Potential Fungal Contamination

    Medline Industries is recalling 1,100 convenience kits nationwide due to potential Aspergillus penicillioides contamination in sterile applicators.

    Product
    Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number: DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3174-2026·2026-09-23

    PTW Freiburg Recalls VERIQA RT MonteCarlo 3D Software Due to Bolus Display Error

    PTW Freiburg is recalling VERIQA RT MonteCarlo 3D software because it fails to clearly display bolus inclusion during secondary dose calculation, which may lead to incorrect dose delivery.

    Product
    Brand Name: VERIQA; Product Name: RT MonteCarlo 3D v3; Model/Catalog Number: S070031.520; Software Version: 3.1.18;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3148-2026·2026-09-23

    Abiomed Recalls Automated Impella Controllers Due to Purge Sensor Defect

    Abiomed is recalling 5,232 Automated Impella Controllers because a purge flag component may fail, causing recognition issues.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, IN; Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3129-2026·2026-09-23

    Nova Biomedical StatStrip Glucose Hospital Meter System Recalled for Software Defect

    Nova Biomedical is recalling StatStrip Glucose Hospital Meter Systems due to a software defect that can cause patient glucose results to be assigned to the wrong medical record.

    Product
    StatStrip Glucose Hospital Meter System. Model No: 66739. Glucose test system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3121-2026·2026-09-23

    Medline Anesthesia Kits Recalled for Fungal Contamination Risk

    Medline is recalling specific lots of Anesthesia L&D A-Line Sets due to potential Aspergillus penicillioides contamination in sterile applicators.

    Product
    Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3132-2026·2026-09-23

    Nova Biomedical Recalls StatStrip Glucose Meters Due to Software Defect

    Nova Biomedical is recalling StatStrip Glucose and B-Ketone meters because a software defect may cause patient data to be assigned to the wrong medical record.

    Product
    StatStrip Glucose and B- Ketone meter. Model No: 66429. Glucose test system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3201-2026·2026-09-23

    Howmedica Recalls Orthopaedic Implants Due to Potential UHMWPE Oxidation

    Howmedica Osteonics Corp. is recalling specific orthopaedic implant components made with aged UHMWPE material. The material may oxidize, leading to increased wear and potential device failure.

    Product
    ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ALL POLY CONSTRAINED INSERT 46MM 69-2246 ALL POLY CONSTRAINED INSERT 48MM 69-2248 ALL POLY CONSTRAINED INSERT 50MM 69-2850 ALL POLY CONSTRAINED INSERT 52MM 69-2852…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0853-2026·2026-09-23

    Pfizer Recalls Dopamine Hydrochloride Injection Due to Sterility Concerns

    Pfizer is recalling specific lots of Dopamine Hydrochloride Injection due to a lack of assurance of sterility. The affected product is distributed nationwide.

    Product
    DOPAMINE HYDROCHLORIDE — DOPAMINE HYDROCHLORIDE (DOPAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3143-2026·2026-09-23

    GE Carescape Central Station Recall for Monitoring Delay

    GE Medical Systems is recalling Carescape Central Station units that may not resume patient monitoring for three minutes after a system restart.

    Product
    Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800 Integrated Part Number 5867474-03 Product Code STV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2985-2026·2026-09-23

    Bard Access Systems Recalls DuoGlide Short-Term Dialysis Catheters

    Bard Access Systems is recalling 22,980 DuoGlide and Niagara short-term dialysis catheters nationwide as a downstream action to a Class I recall.

    Product
    DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625200; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625240; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625300; DuoGlide Short-Term Curved…
    Category
    Medical Device
    Distribution
    50 states
  • SevereFDA (Devices)·Z-3196-2026·2026-09-23

    Howmedica Recalls OMNIFIT Series I Acetabular Inserts Due to Material Wear

    Howmedica Osteonics Corp. is recalling OMNIFIT Series I acetabular inserts because aged polyethylene material may cause excessive wear and device failure.

    Product
    OMNIFIT SERIES I ACET. INSERT 10¿ 22mm ID Catalog No. 2001-2246 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3080-2026·2026-09-23

    BD Alaris Pump Infusion Sets Recalled for Performance Data Discrepancies

    BD Switzerland is recalling BD Alaris Pump Infusion Sets due to discrepancies in performance data that may lead to inappropriate pump performance.

    Product
    BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10015861A 10885403232626 50885403232624 BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Back…
    Category
    Medical Device
    Distribution
    54 states
  • SevereFDA (Devices)·Z-3206-2026·2026-09-23

    Howmedica Recalls Scorpio Patella Implants Due to Polyethylene Wear Risk

    Howmedica is recalling specific Scorpio patella implants because aged polyethylene material may cause excessive wear, leading to device failure and potential revision surgery.

    Product
    SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3123-2026·2026-09-23

    Medline Convenience Kits Recalled for Fungal Contamination Risk

    Medline Industries is recalling 447 convenience kits nationwide due to potential fungal contamination that could cause serious health consequences.

    Product
    Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL LINE ST JOES SYR PACK, Catalog Number: DYNJ38145F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3150-2026·2026-09-23

    Abiomed Recalls Impella Optical Controllers Due to Purge Sensor Defect

    Abiomed is recalling Impella Optical Controllers because a purge flag component may fail, causing recognition issues. The recall covers 4,100 units distributed in the US and internationally.

    Product
    Impella Optical Controller, Automated Impella Controller, Impella Connect Package with the below product descriptions and corresponding Product Codes. 1. Optical, AIC, Impella Connect, Packaged, AU; Product Code: 0042-0040-AU. 2. Optical, AIC, Impella Connect, Packaged, CA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3195-2026·2026-09-23

    Howmedica Recalls Aged Orthopaedic Implant Components Due to Wear Risk

    Howmedica is recalling 12,156 orthopaedic implant components made with aged polyethylene material. The aging may cause excessive wear, leading to device failure and potential need for revision surgery.

    Product
    AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3204-2026·2026-09-23

    Howmedica Recalls Trident Polyethylene Knee Inserts Due to Material Aging

    Howmedica Osteonics Corp. is recalling Trident polyethylene knee inserts because aged raw material may cause excessive wear and device failure.

    Product
    TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components manufactured from UHMWPE (polyethylene)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3124-2026·2026-09-23

    Medline Convenience Kits Recalled for Fungal Contamination Risk

    Medline is recalling 10,407 convenience kits containing sterile applicators that may be contaminated with Aspergillus penicillioides, posing a risk of serious infection.

    Product
    Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3) ACC010679, Catalog Number: ACC010679; 4) ACC010726A, Catalog Number: ACC010726A; 5) DYNDB3061, Catalog Number: DYNDB3061; 6) DYNDH1245, Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1336-2026·2026-09-23

    Foods Alive Organic Moringa Leaf Powder Recalled for Salmonella Risk

    Foods Alive Inc. is recalling 1,691 pouches of organic moringa leaf powder due to potential Salmonella contamination. The product was sold nationwide in the US and UAE.

    Product
    Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3108-2026·2026-09-23

    AVID Medical Recalls Halyard IV Start Kits Due to Mold Contamination

    AVID Medical is recalling Halyard IV Start Kits because they contain applicators contaminated with Aspergillus penicillioides.

    Product
    Halyard IV START KIT NON-STERILE REF: KRIV26-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3130-2026·2026-09-23

    Nova Biomedical StatStrip Glucose Meter Recalled for Data Error

    Nova Biomedical is recalling StatStrip Glucose meters due to a software defect that may assign patient test results to the wrong medical record.

    Product
    StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system.
    Category
    Medical Device
    Distribution
    Distributed nationwide