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Week of June 1–7, 2026

The week in recalls

The week's recalls were mostly medical devices, with a pair of high-risk notices standing out: a pediatric care bed that can trap children and a coolant-contaminated antacid. Drivers also got warnings.

Recall CanaryUpdated

Here's this week's recall roundup. There were 81 recalls, and most were medical devices. The ones that matter most are a pediatric care bed that can trap children and a contaminated antacid, so let's start there.

The KayserBett IDA Pediatric Care Bed is a high risk recall. If the hand control is not locked with the provided key when a child is unattended, the child or other children can operate it and become trapped under the bed frame or between the bed frame and the floor. That can lead to serious injuries or death. If you use this bed, check that the hand control is locked whenever a child is left alone, and follow the instructions for the key.

Gas-X Extra Strength Softgels were recalled because they may be contaminated with a diluted propylene glycol-based coolant from a machine leak during packaging. This is a high risk recall. The coolant could cause nausea, vomiting, and abdominal pain. If you have these softgels, do not take them. Also, Yamaha XTZ690 motorcycles from 2025 have turn signals that may fail, and the recall carries a do not drive warning. If you own one, do not ride it until the turn signal issue is fixed.

Those are the recalls worth your attention today. You can find the full list for the week below, with details on each one and what to do if you have the product.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 81 recalls listed by then.

All 81 recalls this week

Newest first

Recalls the agencies dated Jun 1 to 7. 23 arrived after the week ended. How this list is made

1 recall that day

BD ChloraPrep Clear Applicators

Sterility problem

High risk, FDA,

14 recalls that day

Nelson & Isa Lacteos Requeson Soft Ricotta

Listeria

High risk, FDA,

Fresenius Kabi Epinephrine Injection

Drug impurity

Low risk, FDA,

DigitalDiagnost C90 Flex/Value/Chest/ER

Device defect

Moderate risk, FDA,

Micromed S.p.A. Natus SD LTM 64 PLUS EEG Amplifier/recorder

Software defect

Moderate risk, FDA,

CGuard Prime Carotid Stent System

Device defect

Moderate risk, FDA,

CORFLO and MIC Safety PEG Kits

Sterility problem

Moderate risk, FDA,

Mahurkar Elite PASS Trays

Labeling error

Moderate risk, FDA,

Allia Angiographic X-Ray System

Device defect

Moderate risk, FDA,

Fresenius Medical Care Bicarby Dialysate

Device defect

Moderate risk, FDA,

Plum Duo Infusion, Duo Precision IV, and Solo Precision IV Pump

Device defect

Moderate risk, FDA,

D.O.R.C. TDC VELOCE Two Dimensional Cutters

Device defect

Moderate risk, FDA,

EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves

Labeling error

Moderate risk, FDA,

Sporetraq Mail-In Spore Testing Service

Processing problem

Moderate risk, FDA,

Yamaha

Yamaha XTZ690 (2025)

Do not drive

High risk, NHTSA,

28 recalls that day

Gas-X Extra Strength Softgels

Chemical contamination

High risk, FDA,

Pearl Milling Company Original Pancake & Waffle Mix Complete

Undeclared milk

High risk, FDA, , Ended

Up & Up Fragrance Free and Fresh Cucumber Scented Baby Wipes

Contamination

High risk, FDA,

Siemens Artis Pheno and Artis Icono Interventional Fluoroscopic X-Ray Systems

Device defect

Moderate risk, FDA,

The Coffee Connexion Cheese, Alfredo and Cream Sauces

Salmonella

High risk, FDA,

Draeger Atlan A350 and A350XL Anesthesia Workstations

Device defect

High risk, FDA,

SSC- Surgical Specialties Sharpoint Microsurgical Knife

Labeling error

Moderate risk, FDA,

KayserBett IDA Pediatric Care Bed

Device defect

High risk, FDA,

Grace Medical Stapes Prosthesis

Labeling error

Moderate risk, FDA,

Da Vinci 5

Device defect

Moderate risk, FDA,

Gudook Adult Bike Helmets

Impact hazard

CPSC,

Crenlux Pool Drain Covers

Entrapment hazard

CPSC,

Little Grape Land Nursing Pillows

Suffocation hazard

CPSC,

Broqixin Pool Drain Covers

Entrapment hazard

CPSC,

SUNS SS6291 Solenoid Interlock Switches

Injury hazard

CPSC,

Children's Tiny Land Play Tents

Injury hazard

CPSC,

Boon NURSH Reusable Baby Bottles

Choking hazard

CPSC,

Vornado SRTH Small Room Tower Heaters

Fire hazard

CPSC,

Wyze Solar Cam Pan Security Cameras

Fire hazard

CPSC,

IC Bus

IC Bus CESB School Buses

Mobility equipment defect

NHTSA,

Jeep

Jeep Wrangler, Wrangler 4XE and Gladiator Vehicles

Fire risk when parked

High risk, NHTSA,

Chrysler

Chrysler Pacifica (2020-2022)

Fire risk when parked

High risk, NHTSA,

Honda

Acura MDX (2014-2020), Honda Passport (2019-2023), Honda Pilot (2016-2022), and Honda Ridgeline (2017-2023)

Vehicle structure defect

NHTSA,

Honda

Honda Accord Hybrid (2023-2026), Honda CR-V Fuel Cell EV (2025-2026), and Honda CR-V Hybrid (2023-2026)

Tire defect

NHTSA,

LifeShare Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98846

LifeShare Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 98845

LifeShare Blood Centers Red Blood Cells, Leukocytes Reduced

Donor screening problem

Low risk, FDA, , Ended, Hospital use

Bloodworks Platelets Extended Dating

Quality testing problem

Low risk, FDA, , Ended, Hospital use

16 recalls that day

Lannett Niacin Extended-Release Tablets

Drug dissolving problem

Moderate risk, FDA,

Guardian Drug Antacid Tablets

Foreign object

Moderate risk, FDA,

Forte BioPharma Xyvona (Levorphanol Tartrate Tablets)

Labeling error

Moderate risk, FDA,

Wilco Peanut Raw Shelled Peanuts

Undeclared tree nut

High risk, FDA,

DeRoyal Covaderm Plus Vascular Access Dressings

Sterility problem

Moderate risk, FDA,

Asclemed USA Duloxetine DR Capsules

Drug impurity

Moderate risk, FDA,

Aligned Medical Fluids Kit

Device defect

Moderate risk, FDA,

Fresenius Kabi Ivenix Infusion System LVP Software

Software defect

High risk, FDA,

GE MAC 5 Resting ECG Analysis Systems

Software defect

Moderate risk, FDA,

CareFusion 303 BD Pyxis Medication Cabinets

Device defect

Moderate risk, FDA,

Bayer Avanta Multi-Patient Administration Tube Sets

Device defect

Moderate risk, FDA,

B Braun Spinal Needle Procedure Kits

Device defect

High risk, FDA,

Entegra

Entegra Qwest SE, Condor, Jayco Granite Ridge, and Melbourne Recreational Vehicles

Electrical system defect

NHTSA,

Jayco

2026 Entegra Qwest and Jayco Melbourne Prestige Recreational Vehicles

Electrical system defect

NHTSA,

Aston Martin

Aston Martin Valkyrie

Brake defect

NHTSA,

American Red Cross Blood Services Blood Components

Moderate risk, FDA, , Ended, Hospital use

15 recalls that day

Prime Food Processing Dried Herring Fish

Botulism

High risk, FDA,

University of California Health Donor Human Milk

Contamination

Moderate risk, FDA, , Ended

Spectra Medical Devices Lidocaine HCl Injection

Sterility problem

Moderate risk, FDA,

Lunds & Byerly's Curry Powder Sweet

Labeling error

Moderate risk, FDA,

Albertsons: 121 products

Undeclared tree nut

Moderate risk, FDA, , Ended

Sato Yunker Energy & Health Herbal Supplement with Vitamins

Wrong nutrient levels

Low risk, FDA,

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Tablets

Drug dissolving problem

Moderate risk, FDA,

Arvis Hip & Knee 2.0 and 3.0 Instrument Set

Device defect

Moderate risk, FDA,

Shimadzu Digital Angiography and Radiography Systems

Device defect

Moderate risk, FDA,

Ram

Braun Ram ProMaster Seat Belts

Seat belt defect

NHTSA,

Kia

Kia Telluride and Kia Telluride Hybrid (2027)

Seat belt defect

NHTSA,

Chrysler

Braun Chrysler Pacifica and Voyager Vehicles

Air bag defect

NHTSA,

Nova Bus

Nova Bus LFS (1997-2002, 2005-2024) and Nova Bus LFS Artic (2009-2014, 2016-2024)

Brake defect

NHTSA,

Daavlin Phothera 200 Phototherapy Devices

Device defect

Moderate risk, FDA,

Creative Compounds Betaine Anhydrous

Foreign object

Moderate risk, FDA, , Ended

7 recalls that day

PhaseOne Antimicrobial Solution

Foreign object

Moderate risk, FDA,

CASE v7.0 Cardiac Testing System

Device defect

Moderate risk, FDA,

HiResolution Bionic Ear System Cochlear Implants

Labeling error

Moderate risk, FDA,

Neptune Smart Docking Station

Device defect

Moderate risk, FDA,

Covidien EndoStitch Polysorb Single Use Loading Unit

Sterility problem

Moderate risk, FDA,

Grand Design

Grand Design Reflection Fifth Wheel Recreational Trailers

Suspension defect

NHTSA,

Philips Azurion 3M12, 3M15, 5M12 and Other Angiography Systems

Device defect

Moderate risk, FDA,

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