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Week of June 8–14, 2026

The week in recalls

Infant formula pulled over botulism risk, and a heart pump controller that can fail mid-treatment. The week's recalls leaned heavily on devices and vehicles.

Recall CanaryUpdated

Another week, another round of recalls. There were 88 recalls this week, and many of them were medical devices and vehicles. The ones that matter most involve an infant formula and a heart pump controller, so let's start there.

Nara Organics Whole Milk Organic Infant Formula was recalled at high risk because it may be contaminated with the bacteria that causes botulism. For babies, that can mean constipation, poor feeding, weak crying and low muscle tone, and it can become serious quickly. If you have this formula at home, stop feeding it and check the recall notice for what to do next. Automated Impella Controller from Abiomed was also recalled because a software error can affect the left ventricular heart pumps it runs, and this controller is used in patients whose hearts need mechanical support, so a failure matters. Hospitals and clinicians should check whether their units are affected.

A couple of others deserve a minute. Arrow International Vascular Access and Catheterization Kits were recalled at high risk because the lidocaine, bupivacaine and saline inside came from a supplier with quality problems, and if the sterile fluid is compromised that is a serious concern. And Ford Expedition vehicles from 2018 to 2024 were recalled because the chrome on the center console can bubble and peel into sharp edges that can cut you.

That is the shape of it. The full list below has every recall from the week, with links to the notices and the details you need to check your own products.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 88 recalls listed by then.

All 88 recalls this week

Newest first

Recalls the agencies dated Jun 8 to 14. 25 arrived after the week ended. Also 1 update to an earlier recall. How this list is made

3 recalls that day

Nara Organics Whole Milk Organic Infant Formula

Botulism

High risk, FDA,

Arrow International Vascular Access and Catheterization Kits

Sterility problem

High risk, FDA,

Waymo

Waymo 5th Generation Automated Driving Systems

Electrical system defect

NHTSA, , Part

15 recalls that day

Fry Pie Factory Pepperoni Rolls

Undeclared milk

Moderate risk, FDA, , Ended

Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments

Manufacturing problem

Moderate risk, FDA,

Inventia Healthcare Chlorthalidone Tablets

Drug dissolving problem

Moderate risk, FDA,

Sandoz Focalin XR Extended-Release Capsules

Labeling error

Low risk, FDA,

IntegraDose Compounding Services Vasopressin Syringes

Wrong drug strength

Moderate risk, FDA,

VistaPharm Kerr Insta-Char Activated Charcoal

Quality testing problem

Moderate risk, FDA,

Medline Convenience Kits

Device defect

Moderate risk, FDA,

Automated Impella Controller (AIC)

Software defect

High risk, FDA,

Winnebago

Winnebago Revel and Winnebago Revel Sport (2026-2027)

Vehicle equipment defect

NHTSA,

Thomas Built Buses

Thomas Built SAF-T-LINER HDX2 School Buses

Vehicle structure defect

NHTSA,

Kawasaki

Kawasaki W230 (2025-2026)

Exterior lighting defect

NHTSA,

Altec

Altec AT Series Aerial Device Vehicles

Transmission or drivetrain defect

NHTSA,

Waltco

Waltco MDV Series Liftgate

Vehicle structure defect

NHTSA, , Part

30 recalls that day

Azuma Foods TAKO WASABI Seasoned Octopus with Wasabi

Undeclared fish

High risk, FDA,

Golden State Medical Supply Niacin Extended-Release Tablets

Drug dissolving problem

Moderate risk, FDA,

Fresh Roast Systems ColorTrack

Device defect

Moderate risk, FDA,

Halyard Pain, Towel, Drape and Eye Bag Packs

Sterility problem

Moderate risk, FDA,

MOSAIQ Oncology Information System

Software defect

Moderate risk, FDA,

Boston Scientific Orca Single Use Air/Water and Suction Valves

Device defect

Moderate risk, FDA,

Merlin Patient Care System (PCS)

Software defect

Moderate risk, FDA,

Boston Scientific Neuromodulation Clik X Anchor

Sterility problem

Moderate risk, FDA,

Boston Scientific CSK and TCN Electrodes

Device defect

Moderate risk, FDA,

Fresenius Medical Care Holdings Bicarby Dialysate

Labeling error

Moderate risk, FDA,

Hasuit 7-Drawer Dressers

Tip-over hazard

CPSC,

The Black Sheep Fam Children's Pajamas

Burn hazard

CPSC,

Arctic Zone Titan Pro Coolers

Choking hazard

CPSC,

Kidisle Coffeemakers

Burn hazard

CPSC,

Hopelight Adult Portable Bed Rails

Entrapment hazard

CPSC,

Houoto 642-2150V Pool Drain Covers

Entrapment hazard

CPSC,

Kitchen HQ Thermal Insulated Bowls

Fire hazard

CPSC,

Joyin Sloosh Dive Sticks

Impalement hazard

CPSC,

LiKee Pull String Teething Toys

Choking hazard

CPSC,

Nimood Adult Portable Bed Rails

Entrapment hazard

CPSC,

School Specialty Plastic Tip Restraint Kits

Tip-over hazard

CPSC,

Timechee Changing Table Dressers

Tip-over hazard

CPSC,

Yamaha Drive2 Electric Fleet Golf Cars

Crash hazard

CPSC,

Yamaha UMAX Bistro and Bistro Deluxe Vehicles

Injury hazard

CPSC,

Great Dane

Great Dane 2026 Champion Dry Van Trailers

Vehicle structure defect

NHTSA,

International

International HV

Brake defect

NHTSA,

E & S Grocery & Bakery Taro Cakes

Undeclared egg

High risk, FDA, , Ended

Altec

Altec AC Series Crane Vehicles

Vehicle equipment defect

NHTSA,

10 recalls that day

Amneal Primidone Tablets

Contamination

Low risk, FDA,

Ascend Laboratories Minocycline Hydrochloride Extended-Release Tablets

Drug dissolving problem

Moderate risk, FDA,

NEURO NOURISH Dietary Supplement

Quality problem

Moderate risk, FDA,

Zep Alcohol Sanitizer Spray

Sterility problem

Moderate risk, FDA,

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit

Device defect

Moderate risk, FDA,

DRAGONFLY Thai Ginger Powder

Chemical contamination

Moderate risk, FDA, , Ended

DT MedTech Hintermann Series Talar Implant

Labeling error

Moderate risk, FDA,

Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC)

Device defect

Moderate risk, FDA,

Park St. Deli Macaroni & Cheese

Undeclared soy

Moderate risk, FDA, , Ended

24 recalls that day

Clover Hill Dairy Cheeses and Soft Ricotta

Listeria

High risk, FDA,

MMB of Louisiana Pasteurized Donor Human Milk

Contamination

Low risk, FDA, , Ended

ESTRELLA, Bebida de Parcha (Passion Fruit Drink)

Undeclared color or additive

Low risk, FDA, , Ended

Farm Rich Pizza Cheese Crunchers

Foreign object

Moderate risk, FDA, , Ended

Medartis APTUS Cannulated Compression Screws

Device defect

Moderate risk, FDA,

EXENT Analyser

Device defect

Moderate risk, FDA,

Galaxy RG Cakes, Rolls and Cheesecakes

Undeclared color or additive

Moderate risk, FDA, , Ended

Ford

Ford Expedition

Vehicle structure defect

NHTSA,

Lincoln

2019 Ford Mustang, Lincoln Nautilus, and Lincoln Navigator Vehicles

Electrical system defect

NHTSA,

Ford

Ford Explorer (2024)

Transmission or drivetrain defect

NHTSA,

Ford

Ford Focus

Fuel system defect

NHTSA,

Cummins Clean Fuel Tech

Cummins Clean Fuel Technologies 75DGE CNG Fuel Systems

Fuel system defect

NHTSA, , Part

Vermeer

Vermeer BC1800XL (2002-2026)

Vehicle equipment defect

NHTSA,

Ford

Ford F-150 (2017)

Electrical system defect

NHTSA,

Midwest Automotive Design

Midwest Automotive Design Athletic Series (2023-2024) and 16 more

Electrical system defect

NHTSA,

Ford

Ford Focus and Fusion Cars

Transmission or drivetrain defect

NHTSA,

Ford

Ford F-150 (2018)

Transmission or drivetrain defect

NHTSA,

Ford

Ford Escape (2017)

Driver visibility defect

NHTSA,

Ford

Ford F-150 (2018-2020) — Exterior Lighting

Exterior lighting defect

NHTSA,

Ford

Ford F-150 (2014)

Transmission or drivetrain defect

NHTSA,

Lincoln

Lincoln Nautilus

Driver assistance defect

NHTSA,

Sagemax Bioceramics NexxZr T Multi Dental Zirconia

Device defect

Moderate risk, FDA,

Blood Bank of Hawaii Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

6 recalls that day

Sun Pharmaceutical Industries Budesonide Inhalation Suspension

Foreign object

Moderate risk, FDA,

Breckenridge Duloxetine Delayed-Release Capsules

Drug impurity

Moderate risk, FDA,

NeoSpan SuperElastic Compression Staple w/Instruments

Labeling error

Moderate risk, FDA,

WeiKFiELD Custard Powder Kesar Pista

Labeling error

Low risk, FDA, , Ended

LifeServe Blood Center Red Blood Cells, Leukocytes Reduced, Irradiated

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Updates to earlier recalls (1)

Records agencies added this week to recalls listed in an earlier week. They are not counted above.

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.

A record an agency added this week to a recall listed in an earlier week, such as an FSIS expansion, is under Updates to earlier recalls and is not counted above.

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