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Week of September 14–20, 2026

The week in recalls

A heavy stretch for medical devices, with infusion pumps and infant breathing support among the products worth a closer look. Food and drug recalls also asked for attention.

Recall CanaryUpdated

Another week of recalls to go through. There were 91 recalls in all, and many of them involved medical devices. The ones that matter most are a set of infusion pumps and controllers used in hospitals, plus a supplement sold as a natural enhancement product, so let's start there.

Hospitals and clinics should check their BD Alaris Pump Infusion Sets and their Abiomed Impella Controllers. The infusion sets were recalled because the performance data for some attributes did not match what the pumps expect, which can lead to the pump delivering fluid in a way it should not. The controllers have a small part in the pressure sensor that can fail, which may stop the controller from recognising the purge cassette. Both are high risk. If your facility uses either, follow the instructions the company sent and check which lots you have.

Two other recalls are worth a minute. CooperSurgical INCA Infant Nasal CPAP Sets can develop a loose connection between the tubing and the nasal cannula, which may drop the pressure a baby needs. And Bettergoods Lemon Alfredo Fettuccine may be contaminated with Listeria, so check your fridge and do not eat it.

The full list below has every recall from the week, with the details you need to check your own supplies and shelves. Take a few minutes with it, and pass along anything that affects someone you know.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 91 recalls listed by then.

All 91 recalls this week

Newest first

Recalls the agencies dated Sep 14 to 20. 23 arrived after the week ended. How this list is made

21 recalls that day

GF Blends Gluten Free Baking Mixes

Undeclared wheat

High risk, FDA,

Endo Dexmedetomidine HCl in 0.9% Sodium Chloride Injection

Foreign object

High risk, FDA,

Philips Achieva, Ingenia, Intera and MR MRI Systems

Software defect

Moderate risk, FDA,

Pearle Vision 1 day (Somofilcon A) Contact Lens

Device defect

Moderate risk, FDA,

bioMérieux VITEK 2 AST-N461 Test Kit

Device defect

Moderate risk, FDA,

Medline Convenience Kits Containing Healthmark Instrument Channel Brushes

Device defect

Moderate risk, FDA,

Philips EPIQ Elite Diagnostic Ultrasound System

Software defect

Moderate risk, FDA,

Elegant Foods Pecorino Toscano D.O.P. Stagionato Cheese Wheels

Listeria

Moderate risk, FDA,

Fresenius Medical Care CombiSet Hemodialysis Blood Tubing Sets

Device defect

Moderate risk, FDA,

Maquet PowerLED 300 Concealed Lighting System

Device defect

Moderate risk, FDA,

SeaSpine Mariner Deformity Extended Polyaxial Head

Device defect

Moderate risk, FDA,

HomeFill Oxygen Cylinders

Labeling error

Moderate risk, FDA,

CooperSurgical INCA Infant Nasal CPAP Sets

Device defect

High risk, FDA,

Midmark IQvitals Zone

Device defect

Moderate risk, FDA,

Olympus EZDilate Endoscopic Balloon Dilators

Labeling error

Moderate risk, FDA,

Menow Sunscreen Pressed Powder SPF35 PA+++

Manufacturing problem

Moderate risk, FDA,

Olympus BiCOAG Hemostasis Probe

Device defect

Moderate risk, FDA,

Heidelberg Engineering SPECTRALIS with Flex Module

Device defect

Moderate risk, FDA,

Winnebago

Winnebago Arka (2027)

Vehicle equipment defect

NHTSA,

Volvo Bus

Volvo 9700 buses

Vehicle equipment defect

NHTSA,

Fleetwood

REV: American Dream (2025-2026), Fleetwood Discovery LXE (2026-2027), Fleetwood Palisade (2026), and 1 more

Electrical system defect

NHTSA,

25 recalls that day

ICU Medical 0.9% Sodium Chloride Injection

Labeling error

High risk, FDA,

Esjay Toddler Busy Board Montessori Toys

Choking hazard

CPSC,

Friedrich Air Conditioning KÜHL Q and KÜHL S Window Air Conditioners

Fire hazard

CPSC,

LANCHEZ Pressure Washers

Electric shock hazard

CPSC,

Melissa & Doug Lights & Sounds Fire Truck Activity Board

Choking hazard

CPSC,

BedsPick Mattresses

Fire hazard

CPSC,

Sauna360 Tylö Halmstad and Kiruna Hybrid Saunas

Fall hazard

CPSC,

Sauna360 Infrared Saunas, Hybrid Infrared Saunas and Infrared Kits

Fire hazard

CPSC,

SHEIN Pull & Chew Montessori Teething Toys

Choking hazard

CPSC,

Basecamp Bicycle Helmets

Impact hazard

CPSC,

Toyworld168 Rainbow Mystery Squishy Bun Toys

Swallowing hazard

CPSC,

Hayward Universal Pool Heaters

Carbon monoxide hazard

CPSC,

Charbroil Bistro Pro Electric Grills

Electric shock hazard

CPSC,

Heinz Real - Vraie Mayonnaise

Undeclared soy

Moderate risk, FDA,

Mon Sire Brie, Soft-Ripened French Cheese

Listeria

High risk, FDA,

Hospira Dopamine HCl Injection

Sterility problem

Moderate risk, FDA,

Hexing Haw Balls Candy

Undeclared color or additive

Low risk, FDA,

Dechra Veterinary Products Puralube Vet Ointment

Manufacturing problem

Moderate risk, FDA,

Pi-Cardia ShortCut Device

Device defect

Moderate risk, FDA,

CADD Yellow Medication Cassette Reservoir with NRFit Connector

Device defect

Moderate risk, FDA,

F & A Foundation Reign Medical Clench Staple System (Compression)

Device defect

Moderate risk, FDA,

Jaguar

Jaguar E-Pace (2021-2024), Jaguar F-Pace (2021-2024), Land Rover Defender (2020-2024), and 6 more

Electrical system defect

NHTSA,

Lexus

Lexus RX, Lexus RX Hybrid, Lexus TX, and 3 more (2026)

Steering defect

NHTSA,

JKMAX Heated Blankets and Heating Pads

Fire hazard

CPSC,

Jerify Magnetic Humanoid Toy Sets

Swallowing hazard

CPSC,

21 recalls that day

J. HIGGS Loaded Bacon & Cheddar Potato Chips

Undeclared soy

Moderate risk, FDA, , Ended

Inventia Healthcare Chlorthalidone Tablets

Drug dissolving problem

Moderate risk, FDA,

Michelle's Bakery Pumpkin Spice No Bake Cookies

Undeclared peanut

Moderate risk, FDA,

Halyard Medical Trays

Sterility problem

High risk, FDA,

Buckhead Tuna

Chemical contamination

Moderate risk, FDA,

Captus 4000e Thyroid Uptake System

Device defect

Moderate risk, FDA,

Abiomed Impella Controllers

Device defect

High risk, FDA,

Medline Convenience Kits for Anesthesia, Minor Procedures, Myringotomy and Cataract Surgery

Sterility problem

Moderate risk, FDA,

Datex-Ohmeda Aisys Anesthesia Systems

Device defect

Moderate risk, FDA,

Stryker Sustainability Solutions Ethicon XCEL Bladeless Trocars

Device defect

Moderate risk, FDA,

Boston Scientific StoneSmart Connect Console

Device defect

Moderate risk, FDA,

Medical Action Blood Culture Collection Kits

Sterility problem

Moderate risk, FDA,

Elegant Foods Carrot Cake, Coconut Flakes, and Golden Raisins

Undeclared allergen

Moderate risk, FDA,

Howmedica Osteonics Orthopaedic Implant Components

Device defect

Moderate risk, FDA,

restor3d Kinos Axiom Total Ankle System with Axiom PSR, Flat-Cut (Cut Guide)

Device defect

Moderate risk, FDA,

Hemospray Endoscopic Hemostat

Device defect

Moderate risk, FDA,

Wild Coast Brew Loose-Leaf Teas

Undeclared color or additive

Low risk, FDA, , Ended

Rivian

Rivian R1S (2022-2027), Rivian R1T (2022-2026), and Rivian R2 (2027)

Backup camera defect

NHTSA,

Rewaco

Rewaco PUR3 GT (2024-2025), Rewaco PUR3 GT Touring (2024-2026), Rewaco RF1 GT Touring (2024-2026), and 2 more

Suspension defect

NHTSA,

Embecta Nano Pro Un-Cannulated Demo Samples

Labeling error

Moderate risk, FDA,

American National Red Cross Red Blood Cells and PF24 Plasma

Sterility problem

Moderate risk, FDA, , Ended, Hospital use

16 recalls that day

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert

Foreign object

Moderate risk, FDA,

Bettergoods Lemon Alfredo Fettuccine

Listeria

High risk, FDA,

Taro Nystatin Cream

Quality testing problem

Moderate risk, FDA,

Amneal Phytonadione Injectable Emulsion

Drug impurity

Low risk, FDA,

Mercer's Ice Cream Sandwiches

Undeclared peanut

Moderate risk, FDA,

VERIQA RT MonteCarlo 3D v3 Software

Software defect

Moderate risk, FDA,

Straumann GM Helix Implant

Device defect

Moderate risk, FDA,

SunMed Tracheal Tube

Device defect

Moderate risk, FDA,

GE Healthcare Centricity Enterprise Archive, Enterprise Archive, Centricity PACS, Centricity PACS Server, Workflow Core Services, and Core Services Hub Software

Device defect

Moderate risk, FDA,

NOxBOXi Nitric Oxide Delivery System

Device defect

Moderate risk, FDA,

Happiest Baby SNOO Sleep Sacks

Device defect

Moderate risk, FDA,

American National Red Cross Apheresis Plasma

Sterility problem

Moderate risk, FDA, , Ended, Hospital use

American Natl. Red Cross Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

BD Alaris Pump Infusion Sets

Device defect

High risk, FDA,

Innovative Blood Resources Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

American National Red Cross Red Blood Cells and Pooled Cryoprecipitated AHF

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

8 recalls that day

A&P Creations biQ-FEL and X10 Natural Enhancement Supplements

Hidden drug ingredient

High risk, FDA,

Halyard IV Start Kits

Contamination

High risk, FDA,

Medline Convenience Kits

Contamination

High risk, FDA,

Safecor Health Fluphenazine HCl Oral Elixir

Quality testing problem

Moderate risk, FDA,

Grand Design

Grand Design Lineage (2026-2027)

Tire defect

NHTSA,

New York Blood Center Enterprises Plasma and Red Blood Cells

Low risk, FDA, , Ended, Hospital use

Nuclein DASH Rapid PCR Instrument

Software defect

Moderate risk, FDA,

LifeShare Blood Center Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

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