Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1926–1950 of 27375

HighFDA (Devices)·Z-0210-2026·2025-10-29
Dual lumen stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 16 Fr/Ch (5.3 mm) 266148 Salem Sump" Stomach Tube, Dual Lumen with Anti
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0238-2026·2025-10-29
BD MAX instruments recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0301-2026·2025-10-29
Optima NX gamma camera recalled over risk of detector falling
GE HealthCare is recalling one Optima NX gamma camera because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Optima NX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0239-2026·2025-10-29
Automated microbiology systems recalled after service credentials were accessed by unauthorized actor
Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0237-2026·2025-10-29
Blood culture systems recalled after service credentials were accessed by unauthorized actor
Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0296-2026·2025-10-29
Maxicam gamma cameras recalled over risk of detector falling from mount
GE HealthCare is recalling 37 Maxicam gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Maxicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0236-2026·2025-10-29
BACTEC FX instruments recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0240-2026·2025-10-29
Veritor Connect software recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 38 BD Veritor Connect Software units after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Veritor Connect Software, labeled as the following: 1. Veritor (NUC), Catalog Number: 444881. Transfers in vitro diagnostic results data on the BD Veritor Plus Analyzer to BD Synapsys.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0295-2026·2025-10-29
Elscint Helix gamma cameras recalled over risk of detector falling
GE HealthCare is recalling three Elscint Helix gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Elscint Helix; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0206-2026·2025-10-29
ENFit sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0233-2026·2025-10-29
Oral thermometer probes recalled after being programmed with rectal configuration
Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.
Product
Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0241-2026·2025-10-29
Interventional fluoroscopy systems recalled over control board corrosion affecting imaging
Philips is recalling 29 Zenition 50 interventional fluoroscopic X-ray systems because corrosion of the image intensifier television control board may cause loss of imaging or poor image quality.
Product
Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-0293-2026·2025-10-29
Elscint SPX6 gamma cameras recalled over risk of detector falling
GE HealthCare is recalling 28 Elscint SPX6 gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Elscint SPX6; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0300-2026·2025-10-29
Millenium MPS gamma cameras recalled over risk of detector falling
GE HealthCare is recalling 54 Millenium MPS gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Millenium MPS; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0232-2026·2025-10-29
Insulin pumps recalled over software defect causing unexpected correction bolus
Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.
Product
t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0214-2026·2025-10-29
Central monitoring stations recalled over reboot loop at specific network sizes
GE HealthCare is recalling 2,306 Carescape Central Stations running software V3.0.5 because the system can enter a continuous reboot cycle, losing central monitoring of connected patients.
Product
GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03; Medical Display, cathode ray tube
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0235-2026·2025-10-29
Microbiology data systems recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUTER OPTIPLEX EPICENTER SPARE, Catalog Number: 441421. 3. Generic NUC 2, Catalog Number: 445398. 4. Nuc 5i5 Os Image Bow 2.X, C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0303-2026·2025-10-29
Nuclear medicine gamma cameras recalled over risk of detector falling from mount
GE HealthCare is recalling 102 Starcam and Camstar gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Starcam/Camstar; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0207-2026·2025-10-29
PVC stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0216-2026·2025-10-29
Immunoassay analyzers recalled over dilution factor anomaly affecting patient results
Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxI 9000 Access Immunoassay Analyzer, Part Number C11137
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0208-2026·2025-10-29
Silicone stomach tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2026·2025-10-29
Gastric sump anti-reflux valves recalled after breakage complaints from excessive force
Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0211-2026·2025-10-29
Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0292-2026·2025-10-29
Elscint SPX4 gamma cameras recalled over risk of detector falling
GE HealthCare is recalling 45 Elscint SPX4 gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Elscint SPX4; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0297-2026·2025-10-29
Millenium gamma cameras recalled over risk of detector falling from mount
GE HealthCare is recalling 1,386 Millenium MG/MC gamma cameras because systems past guaranteed service may have been moved without adequate detector support, risking a detector fall.
Product
Millenium MG/MC; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
Category
Medical Device
Distribution
0 states

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1926–1950 of 27375