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.

Which agencies issued them

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.

26926–26950 of 76394

SevereFDA (Drugs)·D-0272-2021·2021-03-03
Teva Recalls Desmopressin Acetate Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Desmopressin Acetate Injection because manufacturing areas exceeded microbial limits, compromising sterility assurance.
Product
Desmopressin Acetate Injection USP, 4 mcg/mL, 1 mL Preserved Vial (NDC 0703-5051-01), packaged in 10X1 mL Vials per Tray (NDC 0703-5051-03), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0276-2021·2021-03-03
Teva Recalls Leucovorin Calcium Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Product
Leucovorin Calcium for Injection, USP, 100 mg/vial, Single-Dose Vial, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-5140-01.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V131000·2021-03-03
Porsche Recalls Macan Models Due to Front Passenger Air Bag Sensor Defect
Porsche is recalling certain 2015-2018 Macan models because the front passenger seat occupancy sensor may fail to detect a passenger, preventing the air bag from deploying.
Product
PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN, MACAN GTS
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0275-2021·2021-03-03
Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns
Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
MethyIPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL, 1 mL Single-Dose Vial (NDC 0703-0031-01), packaged in 25X1ML per tray (NDC 0703-0031-04), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0279-2021·2021-03-03
Teva Recalls Vecuronium Bromide Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling specific lots of Vecuronium Bromide for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Vecuronium Bromide for Injection, 10 mg, 1 mg/mL when reconstituted to 10 mL, 10 mL Vial (NDC 0703-2914-01), packaged in 10 x 10 mL Vials per tray (NDC 0703-2914-03), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0285-2021·2021-03-03
Teva Recalls Leucovorin Calcium Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Leucovorin Calcium for Injection, USP, 350 mg/vial, Rx only, labeled as a) Teva Parenteral Medicines, Inc., Irvine, CA 92618, and b) Manufactured By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, novaplus+, NDC 0703-5145-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0284-2021·2021-03-03
Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns
Teva Pharmaceuticals is recalling 15,043 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/5 mL (80 mg/mL), 5 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0063-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1149-2021·2021-03-03
Steris Recalls OT1000 Series Orthopedic Surgical Tables Due to Bond Separation
Steris is recalling 272 OT1000 Series Orthopedic Surgical Tables because a glued bond may separate, potentially causing unexpected movement during procedures.
Product
OT1000 Series Orthopedic Surgical Tables
Category
Medical Device
Distribution
40 states
SevereFDA (Drugs)·D-0274-2021·2021-03-03
Teva Recalls Epoprostenol Sodium Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Epoprostenol Sodium for Injection, 0.5 mg/vial (500,000 ng), 1X10ML vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-1985-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0273-2021·2021-03-03
Teva Recalls Sterile Diluent for Epoprostenol Sodium Due to Sterility Concerns
Teva Pharmaceuticals is recalling specific lots of Sterile Diluent for Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Sterile Diluent for Epoprostenol Sodium for Injection, 50 mL vial (NDC 0703-9258-01), packaged in 2X50ML per tray (NDC 0703-9258-09), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0278-2021·2021-03-03
Teva Recalls Toposar Etoposide Injection Due to Sterility Assurance Issues
Teva Pharmaceuticals is recalling Toposar (etoposide) injection vials because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Toposar (etoposide injection USP), 1 gram/50 mL (20 mg/mL), 50 mL Multiple-dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-5657-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0282-2021·2021-03-03
Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns
Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0045-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0280-2021·2021-03-03
Teva Recalls Epoprostenol Sodium Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Epoprostenol Sodium for Injection, 1.5 mg/vial (1,500,000 ng), 10 mL vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-1995-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0271-2021·2021-03-03
Teva Recalls Dacarbazine Injection Due to Sterility Assurance Concerns
Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Product
Dacarbazine for Injection USP, 200 mg, Single Use Vial (NDC 0703-5075-01), packaged in 10X20 ML Single Use Vials per tray (NDC 0703-5075-03); Rx only, TEVA Pharmaceuticals USA, INC., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
HighCPSC·21090·2021-03-03
Haro Recalls Masi Bicycles Due to Fork Steerer Tube Breakage Hazard
Haro Bicycles is recalling approximately 510 Masi Evoluzione and Gran Corsa bicycles from model years 2017-2020 because the fork steerer tube can break, causing riders to lose control and fall.
Product
Model Year 2017-2020 Masi Evoluzione and Gran Corsa bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1136-2021·2021-03-03
Ortho-Clinical Recalls Deformed VITROS Chemistry VersaTips
Ortho-Clinical Diagnostics is recalling deformed VITROS Chemistry VersaTips that may cause assay results to be biased by up to +/-16%.
Product
VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and reagent fluid for MicroWell assays. In addition, VersaTips are used to dispense R1 Reagent Fluid into cuvettes in combination with sample fluid for Micro Tips…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1147-2021·2021-03-03
Northgate Recalls ConMed Abdominal Insufflators Due to Incorrect Tubing Material
Northgate Technologies is recalling 25 ConMed 50L abdominal insufflators because an internal tubing component was made with untested material.
Product
ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum) to allow the insertion of a variety of surgical instruments through the abdominal wall for visual examination of the interior or…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V133000·2021-03-03
Altec Recalls 2017-2019 Wood Chippers Due to Exhaust Leak Fire Risk
Altec is recalling 2017-2019 DC1317 and DRM12 wood chippers because a flexible exhaust pipe section may separate, creating an exhaust gas leak that increases the risk of a fire.
Product
ALTEC — ALTEC DC1317 CHIPPER, DRM12 WOOD CHIPPER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1143-2021·2021-03-03
Natus EDS 3 CSF External Drainage System Recalled for Pyrogen Test Failure
Natus Manufacturing Limited is recalling 7 units of the EDS 3 CSF External Drainage System because the device failed to meet pyrogen test requirements for endotoxins.
Product
Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product Usage: indicated for draining cerebrospinal fluid (CFS) from the cerebral ventricles or the lumbar subarachnoid space as a means of reducing intracranial pressure and CSF volume when the insertion of a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1137-2021·2021-03-03
Respironics Recalls 94 Philips Ventilator Batteries Due to Design Verification Issues
Respironics is recalling 94 Philips V60 ventilator batteries because they were shipped without proper design verification. The recall covers distribution across multiple U.S. states.
Product
PHILIPS BATTERY, V60 14.4V, 11.0 Ah, 163 Wh, REF 1076374(1058272), LOT M94663-P1 - Product Usage: The ventilator is intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1145-2021·2021-03-03
Smiths Medical Recalls Bivona Cuffless FlexTend Tracheostomy Tubes Due to Packaging Error
Smiths Medical is recalling specific lots of Bivona Cuffless FlexTend Tracheostomy Tubes because they may have been packaged with the wrong neck flange, posing a risk of patient injury.
Product
Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots 3991171, 3991172, and 3988103) V Neck Flange 4.5mm - Product Usage: intended to provide direct airway access for a tracheotomized patient for up to 29 days. It…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V135000·2021-03-03
Nissan Recalls 2016-2019 Sentra Vehicles for Brake Light Switch Defect
Nissan is recalling 2016-2019 Sentra vehicles because a contaminated brake light switch may prevent brake lights from illuminating, increasing crash risk.
Product
NISSAN — NISSAN SENTRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1142-2021·2021-03-03
Recall of Parietex Hydrophilic Anatomical Mesh Due to Incorrect Side Labeling
Covidien is recalling Parietex hydrophilic anatomical mesh where the package label indicates left-side use but contains a right-side device. This labeling error can lead to implant failure and hernia recurrence.
Product
Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V132000·2021-03-03
2021 Volkswagen Atlas Wheels May Separate Due to Machining Defect
Volkswagen is recalling certain 2021 Atlas and Atlas Cross Sport vehicles due to improperly machined wheel lug bolt holes that may prevent wheels from attaching properly, risking wheel separation and crashes.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1146-2021·2021-03-03
Silk Road Medical Recalls ENROUTE Transcarotid Stent Systems Due to Detachment Risk
Silk Road Medical is recalling 455 ENROUTE Transcarotid Stent Systems because the tip/nose cone may detach from the device.
Product
ENROUTE Transcarotid Stent System REF SR-XXYY-CS
Category
Medical Device
Distribution
43 states