State

District of Columbia product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22826–22850 of 76301

HighFDA (Devices)·Z-0634-2022·2022-02-16
Universal Chuck Surgical Instrument Handle May Detach and Release Ball Bearings
The Universal Chuck instrument handle may loosen and release ball bearings onto the surgical field. If not recovered, these bearings could delay surgery and potentially cause infection or tissue damage.
Product
Universal Chuck-The Universal Chuck is an Instrument Handle provided as an alternative instrument available for use in the TN-ADVANCED" Tibial Nailing System (TNA), TFN-ADVANCED" Proximal Femoral Nailing System (TFNA), RFN-ADVANCED" Retrograde Femoral Nailing System (RFNA)…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22083·2022-02-16
Valco Baby Snap Duo Trend Strollers recalled for front wheel breakage hazard
Valco Baby is recalling Snap Duo Trend strollers because the front wheels can break off during use, causing the stroller to fall unexpectedly. Consumers should stop using the stroller immediately and contact Valco Baby for a free replacement wheel assembly.
Product
Valco Baby Snap Duo Trend Strollers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0632-2022·2022-02-16
Orthopedic knee replacement component recalled for adhesive residue contamination
DePuy Orthopaedics is recalling 3 units of ATTUNE REVISION DISTAL FEMORAL AUGMENT due to adhesive residue that could cause tissue irritation or infection if not detected before surgery.
Product
ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0601-2022·2022-02-16
GE Healthcare MRI Cryogen Ventilation System Defect Recall
GE Healthcare is recalling 17,228 MRI systems due to a potential defect in the cryogen ventilation system that may not meet venting requirements. This Class II recall affects systems distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Optima MR450w 1.5T, Optima MR450w GEM system, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V567000·2022-02-16
2017-2021 Freightliner Cascadia Brake Lights May Remain Illuminated
Daimler Trucks North America is recalling 2017-2021 Freightliner Cascadia trucks because brake lights may remain illuminated after braking. This increases crash risk by making drivers unaware of actual braking.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0618-2022·2022-02-16
GE Healthcare MRI Systems Cryogenic Ventilation System Failure Recall
GE Healthcare is recalling 17,228 MR Vectra MRI systems because the cryogenic ventilation system may not meet required venting specifications.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare MR Vectra System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0609-2022·2022-02-16
GE Healthcare 1.5T SIGNA MRI systems recalled for ventilation defect
GE Healthcare is recalling 17,228 of its 1.5T SIGNA HDe MR imaging systems because the cryogenic ventilation system does not meet required venting standards.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare 1.5T SIGNA HDe MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0587-2022·2022-02-16
QC Control Materials KWIK-STIK AST-GP Produce Incorrect Test Results
Microbiologics Inc recalls KWIK-STIK AST-GP quality control materials that produce incorrect antibiotic susceptibility test results. Two lot numbers were distributed worldwide.
Product
QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V090000·2022-02-16
2022 Lucid Air suspension defect may cause brake failure and loss of control
Lucid Motors is recalling certain 2022 Lucid Air vehicles due to a failing snap ring in the front strut damper. This defect may result in sudden loss of ride height or brake line damage, increasing the risk of a crash.
Product
LUCID — LUCID AIR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0620-2022·2022-02-16
GE Healthcare Optima MR430s MRI systems have potential cryogenic ventilation defect
GE Healthcare recalled MR430s MRI systems because the cryogenic ventilation system may not meet required venting standards, creating potential safety risks.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Optima MR430s System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0600-2022·2022-02-16
GE Healthcare MRI Systems Recalled for Cryogen Ventilation Issue
GE Healthcare is recalling 17,228 SIGNA Artist MRI systems due to a potential defect in the cryogen ventilation system that may not meet safety venting requirements.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0607-2022·2022-02-16
GE Healthcare SIGNA MR Systems cryogenic ventilation system defect recall
GE Healthcare recalled approximately 17,228 SIGNA MR magnetic resonance imaging systems because the cryogenic ventilation systems may not meet proper venting requirements. The defect could create potential safety hazards.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA OpenSpeed MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0603-2022·2022-02-16
GE Healthcare MRI systems recalled for cryogen ventilation defect
GE Healthcare is recalling certain MRI systems because the cryogen ventilation system does not meet venting requirements. The defect could affect safe operation of the MRI magnet.
Product
GE Healthcare MR superconducting magnets, a component of GE 1.5T SIGNA HDx MR System, GE 3.0T SIGNA HDx MR System, GE 1.5T SIGNA HDxt MR System, GE 3.0T SIGNA HDxt MR System, 1.5T SIGNA HDxt, 3.0T SIGNA HDxt, 1.5T SIGNA HDxt Mobile, 3.0T SIGNA HDxt Mobile, SIGNA HDi, SIGNA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0619-2022·2022-02-16
GE Healthcare MR superconducting magnets recalled due to cryogen ventilation system defect
GE Healthcare has recalled 17,228 MR superconducting magnets used in nuclear magnetic resonance imaging systems because the cryogen ventilation system does not meet required venting standards. The recall affects devices distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare MR MAX System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V083000·2022-02-16
2021-2022 Ford Mustang Front Passenger Knee Air Bag Weld Defect
Ford is recalling 2021-2022 Mustang vehicles due to insufficient welds on the front passenger knee air bag, which could deploy improperly and increase injury risk during crashes. Affected owners should contact dealers for a free replacement.
Product
FORD — FORD MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0614-2022·2022-02-16
GE SIGNA MRI Systems Recalled for Cryogen Ventilation Defect
GE Healthcare is recalling 17,228 MRI systems with a potential cryogen ventilation system defect that may not meet regulatory venting requirements.
Product
GE Healthcare MR superconducting magnets, a component of GE SIGNA 3.0T with Excite MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V084000·2022-02-16
Audi Recalls 2022 E-Tron GT for Rear Seat Belt Wiring Issue
Audi is recalling 2022 E-Tron GT vehicles because the center seat belt wiring harness may block access to child seat anchors, preventing proper securing.
Product
AUDI — AUDI E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0566-2022·2022-02-16
Avanos MIC Percutaneous Gastrostomy Kit Recalled for Bolster Sizing Defect
Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy PEG Kit because the external retention bolster may be larger than the tube, creating a risk of improper fit and potential device failure.
Product
MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0590-2022·2022-02-16
GE Healthcare MRI Systems Cryogen Ventilation System Defect Recall
GE Healthcare is recalling SIGNA Premier MRI systems due to a cryogen ventilation system that does not meet venting requirements. Approximately 17,228 affected devices were distributed worldwide.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Premier System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0592-2022·2022-02-16
GE Healthcare MRI superconducting magnets recalled for improper cryogen venting
GE Healthcare has recalled SIGNA Pioneer MRI systems due to potential cryogen ventilation defects that do not meet safety requirements. Approximately 17,228 devices are affected nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Pioneer System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22081·2022-02-16
American Landmaster Utility Vehicles Recalled for Steering Shaft Separation
American Landmaster has recalled about 1,050 utility vehicles (EV, L3, L4, L5, L5W, and L7 models) because the steering shaft can separate from its joint, causing loss of control and crash hazards. Seven steering shaft separations have been reported with no injuries yet.
Product
American Landmaster EV, L3, L4, L5, L5W and L7 Utility Vehicles (UTVs)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V086000·2022-02-16
2019 Volkswagen Atlas: Missing GVWR Label on Side-Step Models
Volkswagen is recalling certain 2018-2021 Atlas and Atlas Cross Sport vehicles equipped with side steps due to a missing GVWR label that reflects the additional weight, increasing overloading risk.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0613-2022·2022-02-16
GE MRI superconducting magnet systems recalled for cryogen ventilation system defect
GE Healthcare is recalling 17,228 MR superconducting magnet systems due to a potential cryogen ventilation system that does not meet venting requirements. The defect could pose safety risks to healthcare facilities and their staff.
Product
GE Healthcare MR superconducting magnets, a component of GE 3.0T SIGNA Infinity TwinSpeed with Excite MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0612-2022·2022-02-16
GE Healthcare MRI superconducting magnets recalled for cryogen ventilation defect
GE Healthcare is recalling 17,228 MRI superconducting magnets that may have improper cryogen ventilation systems. The defect could fail to properly vent cryogenic materials in the SIGNA 3.0T MR System.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA 3.0T MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0589-2022·2022-02-16
QC Blood Culture Identification Panel Recall for Incorrect Antibiotic Susceptibility Test Results
Microbiologics recalls KWIK-STIK blood culture identification quality control panels due to incorrect susceptibility test results. High-level Gentamicin Synergy values were out of specification, risking inaccurate diagnostic guidance.
Product
QC Sets and Panels, KWIK-STIK Blood Culture Identification (BCID) Verification Panel (Live Culture). KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms
Category
Medical Device
Distribution
Distributed nationwide