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Week of November 2–8, 2026

This week so far

47 recalls so far from FDA, CPSC and NHTSA, two rated high risk by the agency.

47 recalls so far this week

Newest first

Recalls the agencies dated Nov 2 to 8, so far. More arrive as agencies publish them. How this list is made

17 recalls that day

HAUOMS Eight-Drawer Dressers

Tip-over hazard

CPSC,

U.S. Titan X-Pro Eagle Youth ATVs

Crash hazard

CPSC,

CAMP X-Dream and X-All Mountain Ice Axes

Fall hazard

CPSC,

Little Giant Ladders with Rapid Locks

Fall hazard

CPSC,

Magnetopia Magnetic Building Cubes and Blocks

Swallowing hazard

CPSC,

Gourmia Digital Air Fryer Ovens

Burn hazard

CPSC,

Arlopu Slide Playsets

Entrapment hazard

CPSC,

Vanderhall Brawley GTS Electric ROVs

Crash hazard

CPSC,

Vevor BMX Bicycles

Crash hazard

CPSC,

Kikea Store X-VESOLJE Nursing Pillows

Suffocation hazard

CPSC,

Baby Brezza SuperFast Sterilizer Dryers

Burn hazard

CPSC,

Slate Cookies & Cream High Protein Nutrition Shake

Labeling error

Not yet rated, FDA,

Ethel's Bakery Gluten Free Turtle Dandy Dessert Bars

Labeling error

Low risk, FDA,

7-Eleven Horchata Drink Concentrate

Not yet rated, FDA,

Luminex LIAISON PLEX Gram-Negative Blood Culture Assay

Device defect

Moderate risk, FDA,

Halyard Arthroscopy Pack

Labeling error

Moderate risk, FDA,

4 recalls that day

GE Senographe Pristina Mammography Systems

Device defect

Moderate risk, FDA,

American National Red Cross Apheresis Platelets

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 100028

American National Red Cross Apheresis Platelets

Processing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 100027

Intelerad IntelePACS Software

Software defect

Moderate risk, FDA,

19 recalls that day

New York Blood Center Enterprises Apheresis Platelets, Leukocytes Reduced, Irradiated

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

ImpactLife Apheresis Platelets, Leukocytes Reduced

Moderate risk, FDA, , Ended, Hospital use

Sagent Pharmaceuticals Famotidine Injection

Foreign object

Not yet rated, FDA,

American Health Packaging Cyanocobalamin Injection

Contamination

Moderate risk, FDA,

Hikma Ciprofloxacin Tablets

Drug impurity

Moderate risk, FDA,

Remel Yeastone Broth

Quality testing problem

Moderate risk, FDA,

Baxter TruSystem 7500 and TruSystem 7000 U Surgical Tables

Device defect

Moderate risk, FDA,

Cochlear Nucleus Nexa Cochlear Implant with Contour Advance Electrode

Manufacturing problem

Moderate risk, FDA,

restor3d Veritas Reverse Total Shoulder Replacement

Device defect

Moderate risk, FDA,

American National Red Cross Apheresis Platelets

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 100025

American Red Cross Apheresis Platelets

Moderate risk, FDA, , Ended, Hospital use

Henry Schein Perma Sharp Surgical Sutures

Unapproved product

Moderate risk, FDA,

Halyard Minor Pack

Sterility problem

Moderate risk, FDA,

Corin Unity Knee ASC Modular Handle

Device defect

Moderate risk, FDA,

Baxter TruSystem 7000 U and 7500 U Operating Tables

Device defect

Moderate risk, FDA,

Hyundai

Hyundai Veloster N and Kona Electric Vehicles

Air bag defect

NHTSA,

7 recalls that day

Tychasis Coats Aloe Lotion, Creme and Liniment

Quality testing problem

Moderate risk, FDA,

Fresenius Medical Care DELFLEX Peritoneal Dialysis Solution

Sterility problem

Moderate risk, FDA,

Edwards Lifesciences Commander M Delivery System

Manufacturing problem

High risk, FDA,

Versiti Michigan Red Blood Cells, Leukocytes Reduced

Moderate risk, FDA, , Ended, Hospital use

Premium Health Care Glutathione Injection Solution

Sterility problem

Not yet rated, FDA,

How this list is made

Each recall is filed under the week of one date, a UTC calendar day. Which date depends on the agency; the recall’s own page names it.

FDA
The day FDA first posted the recall to its Enforcement Report (“Posted” on the recall page), or the day the company’s announcement appeared on FDA’s recalls page, if that came first (“Company announced”). When the day FDA posted it is not known, the day FDA classified it (“Classified”); when we listed the recall before any FDA date, the day we first listed it (“Listed on this site”). FDA’s weekly Enforcement Report, and news roundups built from it, often list the same recall a week or two later.
USDA FSIS
The day FSIS announced the recall or public health alert (“Announced”). An expanded recall keeps its first date.
CPSC
The recall date CPSC published (“Announced”).
NHTSA
The day the manufacturer filed its defect report with NHTSA (“Reported”). NHTSA publishes it days to weeks later, so vehicle recalls keep arriving after a week ends, and news coverage often comes a week or two after the week they are listed in.

Biologics are recalls by FDA’s biologics center (CBER), such as blood, tissue and vaccines, and blood bank equipment. They are usually handled by hospitals, clinics, blood banks and doctors’ offices, not bought in stores. Antibody drugs and other therapeutic biologics that FDA regulates as drugs are listed under Drugs, as FDA files them.

Once a week is over, Recall Canary writes a short post about it from the agencies’ records of that week’s listed recalls only, and rewrites it when they change. Each recall’s own page has the agency’s notice and what to check.

A recall the agency later withdrew stays listed with no risk level, and its own page is marked Withdrawn. A recall notice not yet matched to an agency record is a notice posted on the FDA or CPSC site (a company’s announcement on FDA’s site, or a CPSC news release) before it is matched to the agency’s recall record.

Not listed here: recalls by states, local agencies, other countries or other federal agencies (such as the EPA or the U.S. Coast Guard), and FDA safety alerts that are not recalls. More about dates and sources