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Week of September 21–27, 2026

The week in recalls

A heavy week for medical devices and blood products, with a few food and vehicle recalls worth your attention. A pair of catheters and a kit that may carry mould top the list.

Recall CanaryUpdated

Here's this week's recall roundup. There were 123 recalls in all, and most of them were medical devices and blood and tissue products. The ones a reader most needs to know about involve catheters and a contaminated start kit, so let's start there.

Boston Scientific is pulling its Imager II Angiographic Catheters because the tip can break off or come loose during a procedure. If that happens, a piece can stay inside the patient or travel through the blood vessels, which may mean a longer procedure or a serious blockage. This is a high risk recall, and it is sold nationwide. If you work in a cath lab or stock these, check your inventory and follow the instructions that came with the notice. AVID Medical also recalled its Halyard IV Start Kits, which may be contaminated with a mould called Aspergillus penicillioides. That mould can cause infection, especially in people who are already unwell, and this is also a high risk recall. Staff should set those kits aside.

Another food recall worth a minute is Berlin Seeds Alfalfa Sprouting Seeds, which may be contaminated with E. coli and Salmonella, which can cause serious infections. If you have a packet at home, do not sprout or eat them. A&D Foods Beef, Pork and Goat Cuts were also recalled because they were produced without inspection, so there is no way to know they were handled safely.

Grand Design is recalling thousands of Reflection Fifth Wheel Recreational Trailers over a solar controller that can send the wrong voltage and damage wiring, raising the risk of a fire or crash. You can find every recall from the week in the full list below.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 123 recalls listed by then.

All 123 recalls this week

Newest first

Recalls the agencies dated Sep 21 to 27. 63 arrived after the week ended. How this list is made

27 recalls that day

Sempio Korean Ginseng Chicken Stew Classic and Rich

Import violation

High risk, FSIS,

Fontanini Pork Sausage Links

Foreign object

High risk, FSIS, , Ended

Ajanta Pharma Ranolazine Extended-Release Tablets

Drug dissolving problem

Moderate risk, FDA,

Philips MRI Scanners and Upgrade Kits

Software defect

Moderate risk, FDA,

NOxBOXi Nitric Oxide Delivery System

Manufacturing problem

Moderate risk, FDA,

American Contract Systems BD Urinary Catheter Trays

Contamination

Moderate risk, FDA,

American Nitrile Blue Nitrile Patient Examination Gloves

Contamination

Moderate risk, FDA,

Volcano Philips IntraSight Plus

Software defect

Moderate risk, FDA,

Heraeus PALACOS Bone Cement Mixing and Application Systems

Device defect

Moderate risk, FDA,

EnCor EnCompass Breast Biopsy and Tissue Removal System Console

Device defect

Moderate risk, FDA,

Merit Medical Embosphere Microspheres

Sterility problem

Moderate risk, FDA,

McKesson, Alere, Fisher Scientific, and Henry Schein hCG Tests

Device defect

Moderate risk, FDA,

ATC

ATC RM900 and RM700 Trailers

Trailer hitch defect

NHTSA,

HeartSine Samaritan PAD Public Access Defibrillators

Device defect

Low risk, FDA,

Saving Sight Cornea

Donor screening problem

Low risk, FDA, , Ended, Hospital use

VisionGift Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Eversight Illinois Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99974

Lifesouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99170

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99169

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99168

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99167

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99166

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99165

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99164

28 recalls that day

Deano's Pasta Pear and Pecorino Triangoli Ravioli

Undeclared shellfish

High risk, FDA,

Lior Brand Cinnamon Ground Seasoning

Chemical contamination

Moderate risk, FDA,

Style Homeware Emerspring Mattresses

Fire hazard

CPSC,

5Color Children's Bike Helmet and Pads Sets

Impact hazard

CPSC,

WinxMatrs Mattresses

Fire hazard

CPSC,

Kesyup-Branded Mattresses

Fire hazard

CPSC,

NEWDERY Power Banks

Fire hazard

CPSC,

ABC Trading Light-Up Glasses, Headbands and Ties

Swallowing hazard

CPSC,

Aitjunz 8-Drawer Dressers

Tip-over hazard

CPSC,

INMO Air3 Smart Glasses

Burn hazard

CPSC,

Almond Joy and Reese's Crunchy Peanut Ice Cream Bar

Labeling error

Low risk, FDA,

Medline Convenience Kits

Contamination

Moderate risk, FDA,

Baxter Pro+ MRS Surfaces for VersaCare

Labeling error

Moderate risk, FDA,

Land Rover

Land Rover Range Rover Sport Vehicles

Vehicle structure defect

NHTSA,

Grand Design

Grand Design Reflection Fifth Wheel Recreational Trailers

Electrical system defect

NHTSA,

Cadillac

Cadillac OPTIQ Vehicles

Electrical system defect

NHTSA,

Land Rover

Land Rover Defender (2024)

Seat belt defect

NHTSA,

New York Blood Center Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

Blood Assurance Red Blood Cells, Leukocytes Reduced

Labeling error

Low risk, FDA, , Ended, Hospital use

West TN Regional Blood Center Apheresis Platelets

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

LifeStream Blood Bank Red Blood Cells, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

OneBlood Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

HCSC-Blood Center Plasma and Red Blood Cells

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99048

14 recalls that day

Mezzetta Golden Greek Peperoncini

Contamination

Moderate risk, FDA,

Berlin Seeds Alfalfa Sprouting Seeds

Salmonella

High risk, FDA,

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops

Sterility problem

Moderate risk, FDA,

Halyard IV Start Kits

Packaging defect

Moderate risk, FDA, , FDA event number 99764

Halyard IV Start Kits

Contamination

High risk, FDA, , FDA event number 99761

New York Embroidery Studio Trinity Non-Surgical Isolation Gown

Device defect

Moderate risk, FDA,

Cardioroot Woven Collagen Coated Vascular Graft

Device defect

Moderate risk, FDA,

Imager II Angiographic Catheters

Device defect

High risk, FDA,

Baxter Volara System

Contamination

Moderate risk, FDA,

Forest River

Forest River Cedar Creek Fifth Wheel Recreational Trailers

Vehicle structure defect

NHTSA,

Land Rover

Land Rover Range Rover Sport

Transmission or drivetrain defect

NHTSA,

Dynamax

Forest River Dynamax Isata Recreational Vehicles

Vehicle equipment defect

NHTSA, , NHTSA campaign number 26V610000

Dynamax

Forest River Dynamax Isata Recreational Vehicles

Vehicle equipment defect

NHTSA, , NHTSA campaign number 26V609000

HCSC-Blood Center Plasma and Red Blood Cells

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99047

28 recalls that day

Wholesome Pantry Organic Unsweetened Apple Sauce

Not yet rated, FDA,

A&D Foods Beef, Pork and Goat Cuts

Produced without inspection

High risk, FSIS,

Kwok Shing American Ginsengs

Chemical contamination

Low risk, FDA,

Macleods Olanzapine Tablets

Drug impurity

Low risk, FDA,

Amneal Exenatide Injection

Device defect

Moderate risk, FDA,

Penn State Health Holy Spirit Red Blood Cells, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

DeRoyal Myocardial Probe 400 Series

Device defect

Moderate risk, FDA,

Cardinal Health 200 Presource Convenience Kits

Contamination

Moderate risk, FDA,

The Blood Connection Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99694

NGenuity Patient Monitor with Capnography (ETCO2)

Device defect

Moderate risk, FDA,

Ford Service Parts

Ford Service Parts 10.1 Inch Center Stack

Backup camera defect

NHTSA, , Part

Ford

Ford Ranger

Backup camera defect

NHTSA,

Nova Bus

Nova Bus LFS (2024-2025)

Brake defect

NHTSA,

American National Red Cross Red Blood Cells, Leukocytes Reduced, Irradiated

Mislabeled product

Moderate risk, FDA, , Ended, Hospital use

The Blood Connection Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99693

OneLegacy Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99928

Eversight Illinois Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99927

OneLegacy Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99926

San Antonio Eye Bank Cornea

Labeling error

Moderate risk, FDA, , Ended, Hospital use

South Dakota Lions Eye Bank Cornea

Donor screening problem

Low risk, FDA, , Ended, Hospital use

Lions Eye Bank of Nebraska Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Tissue Transplant Technology Bone

Contamination

Moderate risk, FDA, , Ended, Hospital use

American Red Cross Red Blood Cells, Leukocytes Reduced

Labeling error

Moderate risk, FDA, , Ended, Hospital use

ImpactLife Pooled Cryoprecipitated AHF

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

American National Red Cross Apheresis Platelets and Red Blood Cells

Processing problem

Low risk, FDA, , Ended, Hospital use

Carter BloodCare Red Blood Cells, Leukocytes Reduced

Processing problem

Low risk, FDA, , Ended, Hospital use

26 recalls that day

Sterling Pharmaceutical Services Lubricant Eye Drops and Ointments

Sterility problem

Moderate risk, FDA,

ARUP Laboratories Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

American National Red Cross Apheresis Platelets

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

Vitalant Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

ForeSight Elite Tissue Oximetry Cable

Labeling error

Moderate risk, FDA,

Dynamax

Forest River Dynamax Grand Sport GT Recreational Vehicles

Fuel system defect

NHTSA,

Abiomed Impella Controllers

Software defect

Moderate risk, FDA,

CorneaGen - Boston Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99913

Iowa Lions Eye Bank Cornea

Moderate risk, FDA, , Ended, Hospital use

CorneaGen - Boston Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99922

OneLegacy Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99919

Rocky Mountain Lions Eye Bank Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Eversight Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Precision Ocular Network - Bartlett Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99916

Precision Ocular Network - Bartlett Cornea

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99915

Eversight Illinois Cornea

Donor screening problem

Low risk, FDA, , Ended, Hospital use, FDA event number 99912

Department of Defense Navy Whole Blood

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

HCSC-Blood Center Apheresis Platelets, Leukocytes Reduced

Processing problem

Low risk, FDA, , Ended, Hospital use

The Blood Center Red Blood Cells, Leukocytes Reduced

Labeling error

Moderate risk, FDA, , Ended, Hospital use

Department of Defense Air Force Red Blood Cells

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Mississippi Blood Services Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98849

Mississippi Blood Services Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98848

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced, Pathogen Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

Eversight Illinois Cornea

Processing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 95801

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