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Week of June 15–21, 2026

The week in recalls

Infant resuscitation systems and a heart pump drew the highest-risk labels, while a pistachio sweet and a batch of chocolate raisins carried food hazards worth a look.

Recall CanaryUpdated

Here's your weekly look at what got recalled. There were 62 recalls this week, and most were medical devices. The ones that matter most are a pair of infant resuscitation systems and a heart pump, so let's start there.

The Giraffe and Panda infant resuscitation systems are used in hospitals to help newborns breathe. A knob that controls how much oxygen is mixed in can loosen, so the system may deliver more or less oxygen than the care team intended. That can be a high risk for a fragile infant. If you work in a hospital or clinic that uses these, check whether your unit is affected and follow the maker's instructions for inspecting and repairing the knob. Separately, the Impella CP Set with SmartAssist is a heart pump that supports blood flow in people with severe heart failure. A low purge pressure alarm can keep sounding, and in some cases the pump may stop providing support. It has been linked to cases in seven states. Clinicians should review the maker's guidance on managing the alarm and have a backup plan ready.

In food, a Halawa Extra Pistachio sweet may be contaminated with Salmonella. It was sold in two states, and that recall has ended, but if you still have some at home, throw it out. A batch of dark chocolate raisins may contain peanuts that are not listed on the label, which matters for anyone with a peanut allergy. That one was sold in a single state, so check your pantry if you bought them.

That's the week's main news. For the full list of everything recalled, including the vehicle and consumer product notices, see below.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 62 recalls listed by then.

All 62 recalls this week

Newest first

Recalls the agencies dated Jun 15 to 21. 20 arrived after the week ended. How this list is made

2 recalls that day

MaxxAir

Airxcel MaxxAir N-Series Maxxfan Rooftop Ventilation Fans

Vehicle equipment defect

NHTSA, , Part

Indian

Indian Motorcycle Company 2026 Chief Vintage Motorcycles

Vehicle equipment defect

NHTSA,

29 recalls that day

MorningStar Farms Plant Protein Nuggets and Sausage Patties

Contamination

Moderate risk, FDA, , Ended

Power Plate Meals Frozen Meatloaf with Garlic Mashed Potatoes

Undeclared egg

Moderate risk, FSIS,

Arizer Solo III Portable Electronic Vaporizers

Fire hazard

CPSC,

BABESIDE Doll and Stroller Toys

Choking hazard

CPSC,

Pyro Diablo "Diablo Rising" Fireworks

Explosion hazard

CPSC,

GOPO TOYS Pull String Teething Toys

Choking hazard

CPSC,

Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller

Fall hazard

CPSC,

CooCooBaby Baby Loungers

Suffocation hazard

CPSC,

Michley Children's Pajamas

Burn hazard

CPSC,

Veseacky Pajama Sets

Burn hazard

CPSC,

Keystone Topical Anesthetic Gels

Packaging defect

Moderate risk, FDA,

Fairhope Roasting Company Cold Brew Coffee Concentrate

Labeling error

Moderate risk, FDA, , Ended

Datex-Ohmeda Giraffe and Panda Infant Resuscitation Systems

Device defect

High risk, FDA,

HeartMate 3 Left Ventricular Assist System Kits, System Controller, and Backup Battery

Device defect

Moderate risk, FDA,

International Food Products Dairy Powders and Dressing Stabilizer

Salmonella

Moderate risk, FDA, , Ended

United Salt Plain and Iodized Salt

Labeling error

Low risk, FDA, , Ended

STAAR ICL Calculation Software

Software defect

Moderate risk, FDA,

Inspire Respiratory Sensing and Stimulation Lead

Labeling error

Moderate risk, FDA,

Adndale Magnesium Glycinate Gummies

Undeclared color or additive

Moderate risk, FDA, , Ended

Impella CP Set with SmartAssist

Device defect

High risk, FDA,

BD Connecta Stopcocks

Device defect

Moderate risk, FDA,

Merit Medical Systems Splashwire Hydrophilic Guide Wire

Packaging defect

Moderate risk, FDA,

Piaggio

Piaggio 2026 Liberty 50 and Liberty 150 motorcycles

Electrical system defect

NHTSA,

Subaru

2026 Toyota BZ, Lexus RZ, and Subaru Solterra Battery Electric Vehicles

Electrical system defect

NHTSA,

Farber Specialty

Farber Specialty 2025 45 MCXCR and 2025-2026 HX620 SBA 6X4 Emergency Vehicles

Vehicle equipment defect

NHTSA,

Cadillac

Cadillac Vistiq

Seat defect

NHTSA,

Beta Bionics iLet Bionic Pancreas

Software defect

Moderate risk, FDA,

Rhode Island Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98960

Rhode Island Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98956

8 recalls that day

Endo Buprenorphine HCl Injection

Quality problem

Moderate risk, FDA,

Howmedica Osteonics Tri TS Baseplate

Labeling error

Moderate risk, FDA,

Medline Urethral Catheters and Procedure Kits

Quality testing problem

Moderate risk, FDA,

GE HealthCare Giraffe OmniBed Devices

Device defect

Moderate risk, FDA,

ConMed AirSeal Access Ports and Obturators

Device defect

Moderate risk, FDA,

Mito Red Light Super Mobile

Device defect

Moderate risk, FDA,

Department of Air Force Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

ImpactLife Red Blood Cells, Leukocytes Reduced

Donor screening problem

Low risk, FDA, , Ended, Hospital use

12 recalls that day

Philips MultiDiagnost Eleva and Allura Xper Systems

Device defect

Moderate risk, FDA,

Nutrisystem Chocolate Cheesecake

Undeclared soy

Moderate risk, FDA,

Al Yaman Halawa Extra Pistachio

Salmonella

High risk, FDA, , Ended

Great Value Hawaiian Rolls

Quality problem

Moderate risk, FDA, , Ended

AMD Medicom Ritmed Neurological Sponges

Contamination

Moderate risk, FDA,

DirectCHECK ACT-LR Whole Blood Quality Control, Level 2

Labeling error

Moderate risk, FDA,

Mid Dolciaria Sicilian Cannoli and Crunchy Gluten Free Cannoli

Undeclared color or additive

Moderate risk, FDA,

Smith & Nephew Trigen Proximal Straight Humeral Nail

Manufacturing problem

Moderate risk, FDA,

Arrogantf Spa Drain Covers

Entrapment hazard

CPSC,

Storyteller Overland

Storyteller Overland GXV Hilt Vehicles

Electrical system defect

NHTSA,

We Are Blood Apheresis Platelets, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Community Blood Center of the Ozarks Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

11 recalls that day

FIRST STREET Dark Chocolate Raisins

Undeclared peanut

High risk, FDA,

Ajanta Pharma Aripiprazole Tablets

Labeling error

Moderate risk, FDA,

Medtronic O-Arm O2 Imaging System

Software defect

Moderate risk, FDA,

ALYON and HarmonyAIR A-Series Surgical Lighting System

Device defect

Moderate risk, FDA,

HarmonyAIR A-Series Surgical Lighting System

Device defect

Moderate risk, FDA,

Forest River

Forest River XLR Toy Hauler Recreational Trailers

Vehicle equipment defect

NHTSA,

Wabash

Wabash Van Trailers

Vehicle structure defect

NHTSA,

Blood Bank of Hawaii Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Coastal Bend Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Suncoast Communities Blood Bank Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98882

Suncoast Communities Blood Bank Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98878

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