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Week of June 22–28, 2026

The week in recalls

Contaminated moringa capsules and an eye ointment carrying bacteria led the list. Between them, the week's recalls touched food, drugs, heart pumps and a large batch of vehicles.

Recall CanaryUpdated

Time for this week's recall roundup. Officials listed eighty-five recalls this week, and they were mostly medical devices and biologics, with food and drugs close behind. The ones that matter most involve a supplement that may carry Salmonella and a compounded eye ointment that may carry bacteria, so let's start there.

TNVitamins Organic Moringa Capsules and Powder may be contaminated with Salmonella, which can cause serious infections, especially in young children, older adults, and anyone with a weakened immune system. This one carries a high risk rating and was sold nationwide, so if you have the capsules or powder at home, stop using them and check the recall notice for what to do next. Separately, MFV Compounding Pharmacy Diclofenac Sodium Eye Ointment was found to contain Bacillus cereus, a bacterium that has no business being in something you put in your eye. It went to eight states. If you have this ointment, do not use it.

Two other recalls are worth a minute. Abiomed Impella CP Sets and Low Profile Introducer Kits carry a high risk rating because a blood clot may form during prolonged use of the introducer, a serious concern for patients relying on these heart pumps. And Hyundai Tucson, Tucson Hybrid, and Tucson Plug-In Hybrid vehicles from the 2025 and 2026 model years may have an instrument panel display that fails, which can raise the risk of a crash.

That is the shape of it for now. You can find every recall from the week, along with the steps to take, in the full list below.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 85 recalls listed by then.

All 85 recalls this week

Newest first

Recalls the agencies dated Jun 22 to 28. 41 arrived after the week ended. Also 1 update to an earlier recall. How this list is made

14 recalls that day

La Colonia Foods Requeson Cheeses

Listeria

High risk, FDA,

TNVitamins Organic Moringa Capsules and Powder

Salmonella

High risk, FDA,

MFV Compounding Pharmacy Diclofenac Sodium Eye Ointment

Contamination

High risk, FDA,

Blue Ribbon Classics French Vanilla

Contamination

Moderate risk, FDA, , Ended

Medline Convenience Kits Containing Recalled Swan-Ganz Catheters

Device defect

Moderate risk, FDA,

Mentor Texas Syringes

Device defect

Moderate risk, FDA,

Diamond Coach

Diamond Coach VIP Motorcoaches

Mobility equipment defect

NHTSA,

Nissan

2025 Nissan Sentra

Transmission or drivetrain defect

NHTSA,

Altec

Altec Digger Derrick

Vehicle equipment defect

NHTSA,

Thomas Built Buses

Thomas Built SAF-T-LINER HDX2 Transit Buses

Electrical system defect

NHTSA,

Thomas Built Buses

Thomas Built SAF-T-LINER HDX2 and EFX2 School Buses

Electrical system defect

NHTSA,

OneBlood Apheresis Red Blood Cells, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99092

OneBlood Apheresis Red Blood Cells, Leukocytes Reduced

Labeling error

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99091

Mississippi Blood Services Apheresis and Red Blood Cells

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

22 recalls that day

High Valley Orchard Chocolate Covered Raisins

Undeclared peanut

High risk, FDA, , Ended

Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough

Undeclared soy

Moderate risk, FDA, , Ended

Molly's Kitchen California Style Pasta Salad

Undeclared milk

High risk, FSIS, , Ended

Povi-One, 10% Povidone-Iodine Oral Antiseptic

Wrong drug strength

Moderate risk, FDA,

Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump

Device defect

Moderate risk, FDA,

Medline Convenience Kits with 10mL Polycarbonate Colored Syringes

Unapproved product

Moderate risk, FDA,

Abiomed Impella CP Sets and Low Profile Introducer Kits

Device defect

High risk, FDA,

Honlyne LED Party Favors

Swallowing hazard

CPSC,

Kith-Branded Children's Loungewear Sets

Burn hazard

CPSC,

Small Fish Montessori Busy Board Toys

Swallowing hazard

CPSC,

Raychy Children's Light Sneakers Unisex

Swallowing hazard

CPSC,

Lomi Roll-On Waxing Kits

Fire hazard

CPSC,

MedPride Baby Oil

Poisoning hazard

CPSC,

Sunderwell XW-A17 Electric Youth ATVs

Crash hazard

CPSC,

Mississippi Blood Services Apheresis Platelets and Red Blood Cells

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

Medic Apheresis Red Blood Cells, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

ARUP Laboratories Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

25 recalls that day

Sun Pharmaceutical Perampanel CIII Tablets

Labeling error

Moderate risk, FDA,

Camber Lacosamide Tablets

Foreign object

Moderate risk, FDA,

El David Gelee, Bonbons with Fruits Soft & Juicy

Undeclared color or additive

Moderate risk, FDA,

ANI Pharmaceuticals Hydroxyzine Hydrochloride Oral Solution

Foreign object

Low risk, FDA,

Philips Telemetry Monitor 5500 1.4 GHz

Labeling error

Moderate risk, FDA,

Lunch Box Kitchen Roast Beef and Cheddar Closed Face Sandwich

Labeling error

Low risk, FDA, , Ended

Persona Revision Trabecular Metal Femoral Distal Augment

Device defect

Moderate risk, FDA,

Thuvera Laser Console

Software defect

Moderate risk, FDA,

Medline Convenience Kits

Device defect

High risk, FDA,

GE Healthcare AW Server 3.2 ext.6.5

Device defect

Moderate risk, FDA,

PReye Vitamin See Antioxidant Preservative Free Eye Drops

Sterility problem

Moderate risk, FDA,

Octopus 4, Evolution, and Evolution AS Tissue Stabilizer

Manufacturing problem

Moderate risk, FDA,

Surgify Halo Surgical Drills and Burrs

Device defect

Moderate risk, FDA,

Stryker Neurovascular Inzone Detachment System

Device defect

Moderate risk, FDA,

Airstream

Airstream Classic (2026) and Airstream Interstate (2025-2027)

Electrical system defect

NHTSA,

Ford

Ford Bronco

Vehicle structure defect

NHTSA,

Lincoln

Ford Expedition (2018-2021), Ford Explorer (2020-2021), Ford F-150 (2021), and 2 more

Transmission or drivetrain defect

NHTSA,

Harbinger Motors

Harbinger Motors Step Van and Stripped Chassis

Steering defect

NHTSA,

Elgin

Elgin Pelican (2024-2026)

Electrical system defect

NHTSA,

New York Blood Center Fresh Frozen Plasma and Red Blood Cells

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Kentucky Blood Center Red Blood Cells, Leukocytes Reduced

Processing problem

Low risk, FDA, , Ended, Hospital use

Vitalant Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

Abbott Determine HIV 1/2 Ag/Ab Combo

Device defect

Moderate risk, FDA,

13 recalls that day

Direct Rx Duloxetine and Cymbalta Capsules

Drug impurity

Moderate risk, FDA,

Acumed Hexalobe Screws

Manufacturing problem

Moderate risk, FDA,

Amgen Corlanor and Sensipar Tablets

Foreign object

Moderate risk, FDA,

Zimmer Off-Axis Comprehensive Shoulder System Reamer Guides

Device defect

Moderate risk, FDA,

Joy Gourmet Foods Lassi

Processing problem

Moderate risk, FDA,

PFM Medical Multi-Snare Sets

Device defect

Moderate risk, FDA,

Ventec Life Systems VOCSN+Pro Package

Device defect

Moderate risk, FDA,

Chevrolet

Chevrolet Express and GMC Savana Vehicles

Steering defect

NHTSA,

Rockford Fosgate

Rockford Fosgate Amplifier Kits

Electrical system defect

NHTSA, , Part

Ricon

Ricon S-Series and K-Series Wheelchair Lifts

Mobility equipment defect

NHTSA, , Part

Medic Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

The Blood Connection Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Rhode Island Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

11 recalls that day

Major Methylergonovine Maleate Tablets

Wrong drug strength

Moderate risk, FDA,

Midwest Legacy Raw Beef Dog Food BLT & Bones

Salmonella

High risk, FDA, , Ended

Ajanta Pharma Fenofibrate Capsules

Manufacturing problem

Moderate risk, FDA,

Philips Avalon Fetal Monitor

Device defect

Moderate risk, FDA,

Boichik Bagels Whitefish Salad, Tuna Salad and Pumpernickel Bagels

Undeclared egg

Moderate risk, FDA,

Intuitive Surgical Da Vinci PSS SP1098

Device defect

Moderate risk, FDA,

TMJ Solutions Bilateral Implants

Device defect

Moderate risk, FDA,

Forest River

Forest River 2025-2026 NOBO, Ibex, and 2025-2027 RPOD Recreational Trailers

Electrical system defect

NHTSA,

Blood Bank of Hawaii Apheresis Red Blood Cells, Pooled Cryoprecipitated AHF and Red Blood Cells

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

ImpactLife Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

LifeShare Blood Center Red Blood Cells, Leukocytes Reduced

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