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 the agency’s own highest classification or reported deaths or serious injuries, 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

17076–17100 of 40124

ModerateFDA (Devices)·Z-2294-2020·2020-06-17
Eizo RadiForce RX360 Medical Monitor Recalled for Display Defect
Eizo Corporation is recalling 1,466 RadiForce RX360 medical monitors because a marble pattern may infrequently appear on the display under certain conditions.
Product
RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The display is not intended for mammography.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2319-2020·2020-06-17
Biomet Proximal Humerus Plating System Recalled for Design History Deficiencies
Biomet is recalling A.L.P.S. Proximal Humerus Plating System units because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 7 HOLE 140MM, Item Number: 110030307 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2316-2020·2020-06-17
Biomet Recalls Proximal Humerus Plating System Due to Incomplete Design Files
Biomet is recalling 16 units of the A.L.P.S. Proximal Humerus Plating System because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 14 HOLE 227MM, Item Number: 110030109 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2306-2020·2020-06-17
Biomet A.L.P.S Proximal Humerus Plating System Drill Block Guide Sleeve Recalled
Biomet is recalling A.L.P.S Proximal Humerus Plating System Drill Block Guide Sleeves because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 3.2MM, Item Number: 110017553 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2324-2020·2020-06-17
Biomet A.L.P.S. Proximal Humerus Plating System Recalled for Design History Deficiencies
Biomet is recalling A.L.P.S. Proximal Humerus Plating System units because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 14 HOLE 234MM, Item Number: 110030409 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2358-2020·2020-06-17
BD FACS Sample Prep Assistant III Recalled for Probe Wear Issues
Becton, Dickinson and Company is recalling 467 units of the BD FACS Sample Prep Assistant III because probes may wear prematurely, causing sample dispensing failures.
Product
BD FACS Sample Prep Assistant (SPA) III - Product Usage: Prep Assistant III is intended to prepare human whole blood for flow cytometric analysis on BD FACSCanto II and BD FACSCalibur flow cytometry systems. Pipetting blood, reagents, and lysing solution using the following…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2310-2020·2020-06-17
Biomet A.L.P.S. T15 Multi-Directional Locking Screw Recalled for Design History Deficiencies
Biomet is recalling A.L.P.S. T15 Multi-Directional Locking Screws because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. T15 Multi-Directional Locking Screw 3.5mm x 60mm, Item Number: 110017960 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2309-2020·2020-06-17
Biomet A.L.P.S. Proximal Humerus Plating System Drill Bit Recalled
Biomet is recalling A.L.P.S. Proximal Humerus Plating System 3.2mm Calibrated Drill Bits because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM CALIBRATED DRILL BIT, Item Number: 110017737 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2293-2020·2020-06-17
Eizo RadiForce GX560 Monochrome LCD Monitor Recalled for Display Defect
Eizo Corporation is recalling 96 RadiForce GX560 monochrome LCD monitors because a marble pattern may infrequently appear on the screen under certain conditions.
Product
RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in displaying radiological images (including full-field digital mammography and digital breast tomosynthesis) for review, analysis, and diagnosis by trained medical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2304-2020·2020-06-17
Biomet 8.0 Cannulated Screw Tap Recalled for Incomplete Design History Files
Biomet is recalling 8.0 Cannulated Screw Taps because they were distributed without completed design history files or design transfer activities.
Product
Biomet 8.0 Cannulated Screw Tap-Bone fixation screw Item Number: 110008467 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2356-2020·2020-06-17
BD FACS Sample Prep Assistant II Recalled for Probe Wear Issues
Becton, Dickinson and Company is recalling 95 units of the BD FACS Sample Prep Assistant II because probes may wear prematurely, causing sample dispensing failures.
Product
BD FACS Sample Prep Assistant (SPA) II - Product Usage: K050191: The BD FACSCanto system with BD FACSCanto clinical software when used with the BD FACS Sample Prep Assistant II /III is intended for use as an in vitro diagnostic device for identification and enumeration of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2301-2020·2020-06-17
Immuno-Mycologics Recalls Histoplasma ID Antigen Due to Contamination
Immuno-Mycologics is recalling 155 vials of Histoplasma ID Antigen because potential reagent contamination may cause false positive test results.
Product
Histoplasma Immunodiffusion (ID) Antigen; The IFU labeling is for multiple products which included Fungal Antigens, Positive Controls and ID Plates,and Immunodiffusion (ID) Plates for use in the ID Test, Histoplasma ID Antigen
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2314-2020·2020-06-17
Biomet Recalls Proximal Humerus Plate Templates Due to Incomplete Design Files
Biomet is recalling A.L.P.S. Proximal Humerus Plate Templates because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE 234MM Item Number: 110025473 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2281-2020·2020-06-17
Siemens Atellica CH Fructosamine Reagent Recalled for Acetaminophen Interference
Siemens Healthcare Diagnostics is recalling Atellica CH Fructosamine Reagent because acetaminophen metabolites may interfere with test results.
Product
Atellica CH Fructosamine Reagent (FRUC), Siemens Material Number 11097637, UDI Number 00630414595580 use in the quantitative measurement of glycated protein (fructosamine) in human serum and plasma for monitoring the blood glucose levels of diabetic patients over the preceding…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2322-2020·2020-06-17
Biomet Recalls Proximal Humerus Plating System Due to Incomplete Design History
Biomet is recalling specific lots of the A.L.P.S. Proximal Humerus Plating System because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 7 HOLE 140MM, Item Number: 110030407 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2337-2020·2020-06-17
Philips SureSigns VM1 Monitor Recalled Due to Unverified Manufacturing Records
Philips is recalling a specific SureSigns VM1 patient monitor because it was not intended for commercial distribution and lacks manufacturing records.
Product
Philips SureSigns VM1SpO2, C02, Rec, model no. 863266 - Product Usage: The SureSigns VM1 is a patient monitor that measures oxygen saturation (Sp02), respiration and CO2. The user interface is designed for fast and intuitive operation.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2317-2020·2020-06-17
Biomet Recalls Proximal Humerus Plating System Due to Design History Deficiencies
Biomet is recalling the A.L.P.S. Proximal Humerus Plating System because it was distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 11 HOLE 190MM, Item Number: 110030208 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2360-2020·2020-06-17
Physio-Control Recalls Infant Child Starter Kits Due to Packaging Seal Issues
Physio-Control is recalling 6,732 Infant Child Starter Kits because the packaging for the reduced energy electrodes was not properly sealed.
Product
Infant Child Starter Kits, Part Number: 3202784-009, containing Infant/Child Reduced Energy Defibrillation Electrodes, for use with LIFEPAK 1000 defibrillator, LIFEPAK 500 defibrillator, and LIFEPAK CR Plus/EXPRESS defibrillator - Product Usage: intended to be used by personnel…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2321-2020·2020-06-17
Biomet Recalls A.L.P.S. Proximal Humerus Plating System for Design Documentation Issues
Biomet is recalling A.L.P.S. Proximal Humerus Plating System plates because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 14 HOLE 234MM, Item Number: 110030309 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2320-2020·2020-06-17
Biomet A.L.P.S. Proximal Humerus Plating System Recalled for Design History Deficiencies
Biomet is recalling A.L.P.S. Proximal Humerus Plating System units because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 11 HOLE 197MM, Item Number: 110030308 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2311-2020·2020-06-17
Biomet A.L.P.S. Proximal Humerus Plating System Locking Pegs Recalled
Biomet is recalling A.L.P.S. Proximal Humerus Plating System 3.2mm Locking Pegs 60mm because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM 3.2MM LOCKING PEG 60MM , Item Number: 110025460 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2359-2020·2020-06-17
Physio-Control Recalls Infant Defibrillation Electrodes Due to Packaging Seal Issues
Physio-Control is recalling infant and child defibrillation electrodes because the packaging was not properly sealed. The recall affects units manufactured between August 2017 and October 2019.
Product
Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000 defibrillator, LIFEPAK 500 defibrillator, and LIFEPAK CR Plus/EXPRESS defibrillator - Product Usage: intended to be used by personnel who are trained on the device…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2318-2020·2020-06-17
Biomet A.L.P.S. Proximal Humerus Plating System Recalled for Design Documentation Deficiencies
Biomet is recalling A.L.P.S. Proximal Humerus Plating System units distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 14 HOLE 227MM, Item Number: 110030209 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2219-2020·2020-06-10
Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.
Product
Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X35MM, Item Number 810M6535 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2210-2020·2020-06-10
Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues
Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.
Product
Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X30MM, Item Number 810M4530 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

17076–17100 of 40124