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

1126–1150 of 27375

SevereFDA (Devices)·Z-1548-2026·2026-03-18
TRUE METRIX GO manuals recalled as Class I over E-5 error guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX GO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX GO Kit/RF4001-01BK, CVS TRUE METRIX GO Kit/RF4007-01, Meijer TRUE METRIX GO Kit/RF4019-01, Fred's Phamarcy TRUE METRIX GO Kit/R
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1547-2026·2026-03-18
TRUE METRIX AIR manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX AIR blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR Kit/REA4011-
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1545-2026·2026-03-18
TRUE METRIX manuals recalled as Class I over E-5 error code guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX Kit/RE4001-01, Leader TRUE METRIX Kit/RE4002-01, Leader TRUE METRIX Meter Only/RE4002-40, CVS TRUE METRIX Kit/RE4007-01SB, GN
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1546-2026·2026-03-18
TRUE METRIX PRO manuals recalled as Class I over E-5 guidance
Trividia Health is recalling owner's booklets and instructions for TRUE METRIX PRO blood glucose meters because the labeling did not give lay users adequate directions for the E-5 error code.
Product
Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE MET
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1552-2026·2026-03-18
Beckman Coulter DxC 700 AU analyzer may stop analyzing after errors
Beckman Coulter is recalling DxC 700 AU analyzers because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
DxC 700 AU, REF: B86444, B86446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1540-2026·2026-03-18
GEM Premier 5000 part 00055430011 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055430011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055430011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1544-2026·2026-03-18
Infant and child defibrillator electrodes recalled over pediatric electrode delamination
Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes, catalogue numbers 11101-000016 and 11101-000017, due to pediatric defibrillator electrode delamination.
Product
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 00721902682483 Infant/Child Reduced Energy Defibrillation Electrodes are pre gelled, self-adhesive, the
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2026·2026-03-18
Beckman Coulter AU5800 analyzer may stop analyzing after database errors
Beckman Coulter is recalling Chemistry Analyzer AU5800 units because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1530-2026·2026-03-18
GEM Premier 5000 PAK part 00055407510 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055407510 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055407510.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1539-2026·2026-03-18
GEM Premier 5000 cartridges may eject repeatedly during analyzer warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 analyzers after confirmed complaints that GEM PAK cartridges may show increased Process Control Solution Not Detected errors during warm-up.
Product
GEM Premier 5000; Model No. 00055430010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1511-2026·2026-03-18
Link Endo-Model SL component 16-2840/05 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/05 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2026·2026-03-18
Raz shower commode chair seat may be reinstalled without engaging brackets
Raz Design is recalling several Mobile Shower Commode Chair models because a vendor modification means the seat may be reinstalled without properly engaging the outside rear seat brackets that hold it in place.
Product
Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DI code: (01)00628758003335 Raz-AT600 (Bariatric Tilt) Mobile Shower Commode C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2026·2026-03-18
Link Endo-Model SL component 16-2840/02 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/02 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1525-2026·2026-03-18
GEM Premier 5000 PAK part 00055360008 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1520-2026·2026-03-18
Link Endo-Model plateau 15-8521/15 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/15;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1534-2026·2026-03-18
GEM Premier 5000 part 00055415008 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415008 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415008.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1556-2026·2026-03-18
Artelon FlexBand Twist anchors failed bacterial endotoxin testing
International Life Sciences is recalling the Artelon FlexBand Twist .12, ref TW012, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1497-2026·2026-03-18
IBA proton therapy system may not interrupt beam when gating fails
Ion Beam Applications is recalling PROTEUS 235 proton therapy systems because a disabled interface means the safety system may not interrupt beam delivery if the external gating signal is lost.
Product
IBA Proton Therapy System - PROTEUS 235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2026·2026-03-18
Link Endo-Model plateau 15-2836/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2836/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2836/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1521-2026·2026-03-18
Link Endo-Model plateau 15-0027/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2026·2026-03-18
Medline Medcrest surgical gowns may delaminate prematurely after recommended laundering
Medline is recalling Medcrest surgical gowns because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2026·2026-03-18
Exactech Ergo modular impactor handle may be missing its cross-pin
Exactech is recalling the Equinoxe Ergo Modular Impactor Handle, model 321-09-05, because the impactor handle may be missing a cross-pin.
Product
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-1557-2026·2026-03-18
Vital Sync remote monitoring may not receive bedside monitor alarms
Covidien is recalling the HealthCast Vital Sync Remote Patient Monitoring System after complaints that alarms from the primary patient bedside monitor were not transmitted to or received by the remote system.
Product
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 /
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1535-2026·2026-03-18
GEM Premier 5000 part 00055415010 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1526-2026·2026-03-18
GEM Premier 5000 PAK part 00055360010 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360010.
Category
Medical Device
Distribution
Distributed nationwide

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1126–1150 of 27375