GE Healthcare LLC recalls
Every recall we track for GE Healthcare LLC — 283 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 8 are rated “stop using now”.
Recalls per year, by danger level
Recalls from GE Healthcare LLC peaked in 2021 (85); 283 since 2017. 3% rated “stop using now”.
All FDA recall records for GE Healthcare LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 3 | 1 | 2 | 6 |
| 2018 | 2 | 20 | 21 | 5 | 48 |
| 2019 | 1 | 41 | 36 | 2 | 80 |
| 2020 | 3 | 14 | 20 | 2 | 39 |
| 2021 | 1 | 17 | 53 | 14 | 85 |
| 2022 | 1 | 6 | 16 | 1 | 24 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
Most common reasons for GE Healthcare LLC recalls
What to do if you have a recalled GE Healthcare LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All GE Healthcare LLC recalls
60 shown- Use cautionMedical device
GE Healthcare LLC recalls SIGNA Premier systems
GE Healthcare recalls SIGNA Premier MRI systems that may have steel fittings instead of brass, which could attract during service and cause injury if magnet is ramped.
GE HealthcareFeb 27, 2026 - Lower riskMedical device
GE Healthcare, LLC recalls (1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;
GE Healthcare recalls specific versions of Centricity Universal Viewer software due to inaccurate distance and area measurements when using Global Stack viewport. Affected units include models 2088026-9XX and 5826659-0XX.
GE HealthcareJul 15, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls SIGNA Premier magnetic resonance scanner, model 5748519.
GE Healthcare recalls SIGNA Premier MRI scanners (model 5748519) due to rare risk of hearing loss from elevated acoustic noise during scans. Affected units have specific GTINs.
GE HealthcareJun 24, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity PACS Software Version 7.0 SP0.0.4.7
GE Healthcare recalls Centricity PACS software version 7.0 SP0.0.4.7 due to failure to process study modification notifications on post-verified exams. Affected units include model 5831882-012 with GTIN 00840682145572.
GE HealthcareJun 14, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint. To view, communicate, process, and display Medical images and data
GE Healthcare recalls Centric: Universal Viewer Zero Footprint software versions 6.0 SP6 to SP11.4 due to potential inaccurate medical image measurements. Affected users should contact GE for details.
GE HealthcareJun 8, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls Service manuals for the CT, PET, or NM table as follows: GT1700/GT1700V/VT1700, GT2000/VT2000, GT2000x/VT2000x, High
GE Healthcare recalls service manuals for CT, PET, and NM tables that may cause injury if service personnel remove wrong screws without proper table supports.
GE HealthcareJun 2, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia
GE Healthcare recalls Aisys CS2 and Avance CS2 anesthesia systems with specific serial numbers due to potential reversal of oxygen and air pressure transducer connections.
GE HealthcareJun 1, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems,
GE Healthcare recalls Avance CS2 and Aisys CS2 anesthesia systems with a crack risk in the base that could cause falls. Affected units have specific serial numbers and GTINs. Contact GE Healthcare for details.
GE HealthcareMay 27, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001. Update 3/10/2023: The following FRU and
GE Healthcare recalls CARESCAPE Central Station V2 models 2082278-001 and 2082279-001 due to potential power supply failure causing loss of patient monitoring. Affected units include specific display and component parts.
GE HealthcareMay 10, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Radiology RA600
GE Healthcare recalls Centricity Radiology RA600 software versions 7.0-7.0 SP and 8.0-8.0 SP14H due to potential inaccurate distance and area measurements on magnified or scaled-down images. Affected units may require software update.
GE HealthcareApr 28, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019
GE Healthcare recalls Avance CS2 and CS2 Pro anesthesia devices manufactured on or after April 1, 2019, due to backup batteries failing earlier than expected. Affected units have specific serial numbers and model numbers listed in the recall.
GE HealthcareApr 25, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls Replacement back up batteries distributed on or after April 1, 2019, for CARESCAPE R860, Engstr¿om Carestation and
GE Healthcare recalls replacement backup batteries for CARESCAPE R860 and Engström Carestations distributed after April 1, 2019, due to risk of ventilator shutdown without AC power.
GE HealthcareApr 18, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c) 3101010-009, d) 3101010-008
GE Healthcare recalls specific MUSE Cardiology Information System models due to risk of lost test measurements and diagnosis statements after signing in the web client. Affected units have unique serial numbers and model identifiers.
GE HealthcareMar 16, 2022 - UnratedMedical device
GE Healthcare, LLC recalls GE Healthcare MR Systems, Magnetic Resonance imaging (MRI). SIGNA Premier, SIGNA Architect, SIGNA Pioneer, Discovery
GE Healthcare is recalling several MRI systems due to a risk of magnet falling during de-installation if hardware isn't properly secured, potentially causing injury. Affected models include SIGNA Premier, SIGNA Architect, SIGNA Pioneer, Discovery, and others. No remedy is specified in the recall notice.
GE HealthcareMar 4, 2022 - Lower riskMedical device
GE Healthcare, LLC recalls Signa 1.5T TwinSpeed Magnetic Resonance Imaging System
GE Healthcare recalls Signa 1.5T TwinSpeed MRI systems due to potential left-right image flips. Affected units have specific system IDs listed in the recall notice.
GE HealthcareFeb 18, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF
GE Healthcare recalls v2.0 Central Station models with unapproved keyboards that may mute alarms, risking missed critical alerts. Affected units include specific serial numbers and versions.
GE HealthcareJan 28, 2022 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance
GE Healthcare recalls SIGNA Artist MRI system magnets due to potential cryogen ventilation system failure. Affected units may not meet venting requirements.
GE HealthcareDec 23, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"
GE Healthcare recalls Vscan Extend devices sold as 'Vscan Extend Sector DICOM' that won't power on because of depleted battery when not turned off before battery removal or computer connection without AC power.
GE HealthcareNov 4, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint Client
GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client versions with incomplete patient imaging study display. Affected units may need software update to prevent image display issues.
GE HealthcareOct 15, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls SIGNA Pioneer nuclear magnetic resonance imaging system
GE Healthcare recalls SIGNA Pioneer MRI systems with software versions PX29.1 and PX25.4 (T) that may show missing slices in 3D images, potentially causing anatomical gaps in scans.
GE HealthcareAug 26, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system
GE Healthcare recalls Centricity Universal Viewer 7.0 software versions due to study changes not saving to archives. Affected units may experience data loss if images are modified.
GE HealthcareAug 12, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is a device that displays medical images (including
GE Healthcare recalls Centricity Universal Viewer and Viewer 6.0 software versions 6.0 through 6.0 SP7.1 due to image acquisition failures and synchronization issues with the Centricity Enterprise Archive.
GE HealthcareAug 6, 2021 - Use cautionMedical device
GE Healthcare, LLC recalls Flow sensors that may be installed in the following GEHC anesthesia machines: (1) Aestiva MRI, GTIN 0080682102339; (2)
GE Healthcare recalls flow sensors installed in certain anesthesia machines made before June 2021. These sensors may cause leaks leading to incorrect anesthesia dosing. Affected models include Aestiva MRI, Aestiva 7900, and others.
GE HealthcareAug 2, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition
GE Healthcare recalls Revolution CT, Revolution CT ES, Revolution Apex, and Revolution CT with Apex edition CT scanners due to potential overdisplay of radiation dose during interventional exams with SmartStep.
GE HealthcareJun 30, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition
GE Healthcare recalls Revolution Apex and Revolution CT with Apex Edition scanners due to potential inaccurate radiation dose displays, which could lead to unnecessary radiation exposure during scans.
GE HealthcareJun 30, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls The system is intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission
GE Healthcare recalls Revolution CT systems due to potential scan group name input errors causing failed updates. Affected units may not confirm scan group additions, risking incomplete imaging. Contact GE for remedy details.
GE HealthcareJun 30, 2021 - Use cautionMedical device
GE Healthcare, LLC recalls AMX Navigate Mobile X-Ray System
GE Healthcare recalls AMX Navigate Mobile X-Ray Systems with unexpected column motion during parking. Affected models include AMXNV2000001WK, AMXNV2000:002WK, DF2401600003WK. Stop using immediately to prevent potential injury.
GE HealthcareJun 24, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Revolution EVO, Optima CT660, Optima CT680 CT Systems.
GE Healthcare recalls Revolution EVO, Optima CT660, and Optima CT680 CT systems due to potential increased X-ray radiation exposure from software options. Affected units have specific hardware codes.
GE HealthcareJun 14, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls SIGNA Premier - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high
GE Healthcare recalls SIGNA Premier MRI scanners where accidentally selecting patient orientation may cause flipped images. Affected units require correction to prevent misdiagnosis.
GE HealthcareJun 4, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls CARESCAPE PDM-Masimo SpO2. Physiological data monitor.
GE Healthcare recalls CARESCAPE PDM SpO2 monitors that may freeze saturation values without power down. Affected models include SA3, SPX with specific part numbers. No action needed if device functions normally.
GE HealthcareMay 21, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Case Cardiac Assessment System for Exercise Testing and CardioSoft Diagnostic System Exercise Stress Testing ECG
GE Healthcare recalls cardiac assessment software versions v6.6x, v6.7x, v7.0 due to risk of patient test reports appearing in incorrect records. Affected users should contact GE for details.
GE HealthcareApr 19, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN
GE Healthcare recalls Innova IGS 3, 5, and 6 x-ray systems with a vertical line defect that splits monitor images. Affected units have specific serial numbers listed in the recall notice.
GE HealthcareApr 19, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer - Product Usage: intended to assist in the viewing, analysis, diagnostic interpretation,
GE Healthcare recalls Centricity Universal Viewer devices that may show incorrect patient comparisons when Cross Enterprise Display is enabled and Workflow Manager launches the viewer. Affected units have specific serial numbers and UDI codes.
GE HealthcareMar 19, 2021 - Use cautionMedical device
GE Healthcare, LLC recalls Revolution CT
GE Healthcare recalls Revolution CT systems due to potential radiation dose inaccuracies. Affected units may deliver higher or lower radiation than prescribed, risking patient safety.
GE HealthcareMar 19, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls NM/CT 860 Nuclear Medicine / CT Scanners
GE Healthcare recalls NM/CT 860 scanners that may shift CT radiation exposure by up to 5cm, risking extra X-rays during specific scans. Affected units sold with GTIN 00840682140751.
GE HealthcareFeb 7, 2021 - Use cautionMedical device
GE Healthcare, LLC recalls System, X-Ray, Tomography, Computed: Revolution CT, Revolution CT ES.
GE Healthcare recalls Revolution CT, Revolution CT ES and related systems due to potential missing/damaged table pinch protectors that could cause lacerations from exposed table screws.
GE HealthcareDec 17, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use
GE Healthcare recalls Precision 600FP radiographic systems due to potential monitor suspension detachment causing patient or operator injury.
GE HealthcareDec 10, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls GE NM/CT 870 CZT system Model Number H3906CW - Product Usage: intended for general Nuclear Medicine imaging procedures
GE Healthcare recalls NM/CT 870 CZT system model H3906CW due to loose rotor bearing screws that may cause a bearing to release during use. Affected units have specific serial numbers listed.
GE HealthcareDec 10, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls Revolution CT ES - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography
GE Healthcare recalls Revolution CT ES X-ray scanners due to potential protocol errors causing patient safety risks. Affected units have specific model and serial numbers. Consumers should contact GE for details.
GE HealthcareNov 23, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls MAC VU360, Electrocardiograph
GE Healthcare recalls MAC VU36: Electrocardiograph model 2030360 001 due to incorrect patient identification and demographic errors. Affected users should contact GE Healthcare for details.
GE HealthcareOct 27, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition, Model 5995000-5 - Product Usage: The system is intended for head,
GE Healthcare recalls Revolution Apex and Revolution CT with Apex Edition models 5995000-5 for potential smudge artifacts that could affect medical imaging accuracy.
GE HealthcareSep 21, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls Flow Sensor Service Part, Catalog 2089610-001-S
GE Healthcare recalls flow sensors from August 2020 with potential small punctures in tubes. Affected models include Aespire 7100/11, Aespire 7900, and others. Stop using if you have these parts.
GE HealthcareSep 17, 2020 - UnratedMedical device
GE Healthcare, LLC recalls System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to
GE Healthcare recalls specific MRI scanners due to potential electrical arc flash in the PGR cabinet. Affected models include 5148810-3, 5741000-100, 5741000-26, and 5741000-27. No remedy details provided in recall notice.
GE HealthcareSep 8, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls NM/CT 850 Model Number: H3907AD
GE Healthcare recalls NM/CT 850 Model H3907AD with loose rotor bearing screws that could cause equipment failure. Affected units have specific serial numbers and system IDs listed in the recall notice.
GE HealthcareAug 14, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls CARESCAPE R860 Ventilator The CARESCAPE R860 ventilator is a microprocessor based, electronically controlled,
GE Healthcare recalls CARESCAPE R860 ventilators with potential oxygen sensor issue causing inaccurate FiO2 display. Affected units have specific identifiers; check your device's serial number. No immediate action needed but monitor for incorrect oxygen readings.
GE HealthcareJul 14, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls CARESCAPE ONE, Physiological Patient Monitor - Product Usage: is both a multi-parameter physiological patient monitor
GE Healthcare recalls CARESCAPE ONE patient monitors that may fail to alert for ventricular fibrillation when docked to specific host monitors, posing a risk of undetected cardiac events.
GE HealthcareJun 22, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls CARESCAPE Patient Data Module (PDM) used with the following monitors: CARESCAPE B450/B650/B850, SOLAR 8000M/I and
GE Healthcare recalls specific CARESCAPE Patient Data Modules used with certain monitors due to risk of false flat line ECG alerts when AEDs are used.
GE HealthcareMay 18, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls Giraffe Incubator with installed Servo Oxygen module. Infant incubator.
GE Healthcare recalls infant incubators with Servo Oxygen modules that may display incorrect oxygen levels, risking infant health. Affected units have specific serial numbers and part kits.
GE HealthcareApr 28, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
GE Healthcare recalls Giraffe Shuttle Upgrade Kits with part numbers 2109672-001 and 2109673-001 due to sulfur odor from battery outgassing during charging. Affected units have specific serial numbers and GTIN.
GE HealthcareApr 2, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner
GE Healthcare recalls SIGNA Architect MRI systems that may record incorrect image dates due to installation workflow issues. Affected units need verification and correction to prevent inaccurate medical records.
GE HealthcareDec 23, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer 6.0, a device that displays medical images and data from various imaging sources, and from
GE Healthcare recalls Centricity Universal Viewer 6.0 SP10+ due to potential misdiagnosis from incorrect grayscale measurements in images with varying pixel sizes. Affected units may require correction to ensure accurate medical imaging.
GE HealthcareDec 16, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Lunar iDXA bone densitometer
GE Healthcare recalls Lunar iDXA bone dens: potential accidental radiation exposure from control panel malfunction. Affected units may need repair or replacement.
GE HealthcareDec 3, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended to provide general inhalation anesthesia and
GE Healthcare recalls Carestation 620/650/650c A2 anesthesia systems due to potential loose cable connections causing loss of mechanical ventilation. Affected units may require immediate attention to prevent hypoxia.
GE HealthcareNov 25, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls ApexPro Telemetry System - Product Usage: The ApexPro Telemetry System is intended for use under the direct supervision
GE Healthcare recalls specific ApexPro Telemetry System units for cybersecurity vulnerabilities that could allow unauthorized network access when connected to hospital networks. Affected units have unique serial numbers listed in the recall notice.
GE HealthcareNov 12, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Giraffe Incubator Carestation, Giraffe Incubator Carestation CS1 infant warmer
GE Healthcare recalls Giraffe Incubator Carestation CS1 infant warmers due to potential patient falls from unsecured panels. Affected units include all model numbers with specific identifiers.
GE HealthcareOct 11, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls CARESCAPE Respiratory Module E-sCAiOV
GE Healthcare recalls CARESCAPE Respiratory Module E-sCAiOV units with potential up to 50% error in oxygen measurements. Affected units have specific serial numbers and lot codes.
GE HealthcareSep 27, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls CardioLab/ComboLab Recording Systems
GE Healthcare recalls CardioLab/ComboLab Recording Systems with specific model numbers and lot codes due to potential failure in patient leakage current test, which could cause electrical shock if connected to other medical devices.
GE HealthcareSep 16, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Achilles Express Bone Sonometer
GE Healthcare recalls Achilles Express Bone Sonometer models with European CEE-7/7 Type Power Cords that lack protective earth connection pins for countries requiring three protruding pins.
GE HealthcareSep 3, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry
GE Healthcare recalls ApexPro Telemetry Server System units that may not provide visual or audible alarms for ECG arrhythmias, ECG leads failure, or pulse oximetry under certain conditions. Affected units have specific serial numbers listed in the recall notice.
GE HealthcareAug 30, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Proteus XR/a (SlOK : K993090)
GE Healthcare recalls Proteus XR/a stationary radiographic systems due to intermittent failure to provide audible exposure indication after imaging. Affected units may not alert users to completed exposures, potentially leading to safety risks during medical procedures.
GE HealthcareAug 9, 2019
GE Healthcare LLC recall questions
How many recalls has GE Healthcare LLC had?
283 recalls from GE Healthcare LLC are on record with U.S. safety agencies, from 2017–2026.
What is the most recent GE Healthcare LLC recall?
GE Healthcare LLC recalls SIGNA Premier systems, dated Feb 27, 2026. Every GE Healthcare LLC recall is listed on this page, newest first.
Why are GE Healthcare LLC products recalled?
The most common reasons on record: Rotor bearing screws were found loose on detector. (8); Flow sensors could have damaged tubes in the form of small punctures or cuts. (7); GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure (6); Potential electric leakage affecting the user. (6).
What should I do if I have a recalled GE Healthcare LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new GE Healthcare LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.