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Week of August 10–16, 2026

The week in recalls

A heavy week for medical devices, with air bubbles in infusion sets and a sterility lapse in a common saline injection. Food and vehicles filled out the rest, including a granola that may carry Salmonella.

Recall CanaryUpdated

Here's your weekly look at what got recalled. Ninety-five recalls were listed this week, and medical devices were the biggest group, with problems that could reach patients directly. Food and vehicles made up much of the rest, and a few of those are worth your attention too.

Baxter's Duo-Vent Solution Set and Male Luer Lock Adapter can develop air bubbles in the drip chamber and tubing, especially when a pressure cuff is in use or the line is flushed wide open. Air in an infusion line can travel to the bloodstream, which is why this one carries a high risk rating. If you use this set at home or in a clinic, check the lot numbers against the recall notice and stop using affected stock. The other device recall worth your attention is Spectra Medical Devices Sodium Chloride Injection, which may not be sterile. That means patients could be exposed to microorganisms or foreign matter, and the agency rates it high risk as well. Clinics and pharmacies in the affected states should pull it and follow the instructions.

Two food recalls also deserve a minute. The Hampton Grocer Lacnola Small Batch Lactation Granola may be contaminated with Salmonella, which can cause serious infections, particularly in people who are pregnant or immune compromised. If you have a bag, do not eat it. And Oma's Pride Pet Food Woof Complete Canine Chicken Recipe may also carry Salmonella, which matters both for the animals eating it and for anyone handling the food.

Drivers should also know about the Chrysler Pacifica and Voyager Vehicles, where the rearview camera image may not appear when you shift into reverse, cutting your view behind the car. Check your VIN if you drive one. The full list below has every recall from the week, with links to the notices and what to do next.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 95 recalls listed by then.

All 95 recalls this week

Newest first

Recalls the agencies dated Aug 10 to 16. 29 arrived after the week ended. How this list is made

24 recalls that day

The Hampton Grocer Lacnola Small Batch Lactation Granola

Salmonella

High risk, FDA,

Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower

Undeclared wheat

High risk, FDA, , Ended

Spectral Instruments Lago X and Ami HTX Imaging Systems

Device defect

Moderate risk, FDA,

Raw Bistro Dog Fare Free Range Turkey Entree Raw Dog Food

Salmonella

High risk, FDA,

Nutrient Protein Cereal Cocoa Crunch

Undeclared soy

Moderate risk, FDA, , Ended

Amneal PEMRYDI RTU (Pemetrexed Injection)

Quality problem

Moderate risk, FDA,

Libtayo (Cemiplimab-Rwlc) Injection

Sterility problem

Moderate risk, FDA,

Paragon 28 Navicular Cage Foot Implants

Device defect

Low risk, FDA,

Blanketrol II, Blanketrol III, and Innercool Coolblue Console

Device defect

Moderate risk, FDA,

Paragonix Technologies KidneyVault Portable Renal Perfusion System

Software defect

Moderate risk, FDA,

Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen

Device defect

Moderate risk, FDA,

Halyard LAVH Packs

Device defect

Moderate risk, FDA,

Getinge Y Sensor Module, Servo-U, Servo-N

Device defect

Moderate risk, FDA,

Boston Scientific OverStitch Suture Cinch and Suture Cinch Long

Device defect

Moderate risk, FDA,

Prospector Popcorn Gourmet Popcorn

Wrong nutrient levels

Moderate risk, FDA,

Tobii Dynavox TD Navio Maxi and Midi Speech Generating Device

Device defect

Moderate risk, FDA,

Arrowhead DE Arrow-LOK Implant

Sterility problem

Moderate risk, FDA,

Kico Knee Innovation Arvis Surgical Navigation System GEN 2

Device defect

Moderate risk, FDA,

Philips Cardiac Workstation 5000 and 7000

Device defect

Moderate risk, FDA,

Dentsply Sirona Capsule Mixer

Device defect

Moderate risk, FDA,

Intersurgical Guedel Oropharyngeal Airways

Device defect

Moderate risk, FDA,

Foundation Medicine Hamilton Microlab STAR Liquid Handler

Software defect

Moderate risk, FDA,

EndoFLIP System

Device defect

Moderate risk, FDA,

Horton

Horton Type I, Type III, and Critical Care Ambulances

Vehicle equipment defect

NHTSA,

33 recalls that day

Grand Central Bakery Potato Sourdough Bread

Foreign object

Moderate risk, FDA,

Shoolin Pharma Chem Sildenafil Citrate and Tadalafil

Manufacturing problem

Moderate risk, FDA,

CLEAR EYES Maximum Itchy Eye Relief

Sterility problem

Moderate risk, FDA,

New York Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

Hoxworth Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99471

Cardinal Health Presource Kits

Contamination

Moderate risk, FDA,

BD Intravascular Administration and Extension Sets

Sterility problem

Moderate risk, FDA,

COMMOWNER Electric Pressure Washers

Electric shock hazard

CPSC,

Cooluli Minifridges

Fire hazard

CPSC,

CuberShop Magnetic Stickerless Speed Cubes

Swallowing hazard

CPSC,

Deli Jerry Fuel Containers

Burn hazard

CPSC,

DUMOS Nine-Drawer Dressers

Tip-over hazard

CPSC,

Zimtown Portable Gas and Fuel Cans

Burn hazard

CPSC,

Merax Murphy Beds

Impact hazard

CPSC,

Goody King Magnetic Building Cubes and Blocks

Swallowing hazard

CPSC,

Hampton Bay Halwin 52-Inch Ceiling Fans

Impact hazard

CPSC,

Qabefy Mattresses

Fire hazard

CPSC,

Ritchey Carbon Fiber Bicycle Forks

Fall hazard

CPSC,

Shengsen Prank Sound Maker

Swallowing hazard

CPSC,

Brookstone-Branded Tabletop Fire Pits

Fire hazard

CPSC,

SUGIFT Electric Pressure Washers

Electric shock hazard

CPSC,

TooyBing Wooden Bead Stacking Toys

Choking hazard

CPSC,

Yamazuki Youth All-Terrain Vehicles (ATVs)

Crash hazard

CPSC,

Ford

Ford Explorer (2026)

Engine defect

NHTSA,

Jeep

2026 Jeep Grand Cherokee and Grand Cherokee L Vehicles

Driver visibility defect

NHTSA,

Dodge

Dodge Durango Vehicles

Vehicle structure defect

NHTSA,

Land Rover

Land Rover Range Rover Vehicles

Steering defect

NHTSA,

Nissan

Nissan Altima (2025) — Air Bags

Air bag defect

NHTSA,

Walter L. Shepeard Community Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use

15 recalls that day

Oma's Pride Pet Food Woof Complete Canine Chicken Recipe

Salmonella

High risk, FDA,

Marketside Tomato Bisque Soup Kit

Listeria

Moderate risk, FDA,

Dairyland Produce Pepper Jalapeno

Salmonella

High risk, FDA,

Whole Foods Guacamole Dips, Salsas and Trio Dip

Salmonella

High risk, FDA, , Ended

LifeShare Blood Centers Apheresis 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, FDA event number 99418

Erbe USA ERBECRYO 2 Cryosurgical Unit

Device defect

Moderate risk, FDA,

ProNephro AKI (NGAL) Reagent Kit

Device defect

Moderate risk, FDA,

BIOFIRE Respiratory Panel 2.1 (RP2.1)

Device defect

Moderate risk, FDA,

BMW

BMW 840i, 540i, M550i xDrive and 750e xDrive Vehicles

Transmission or drivetrain defect

NHTSA,

BMW

BMW X3

Steering defect

NHTSA,

Grote

Grote Marker Lights

Exterior lighting defect

NHTSA, , Part, NHTSA campaign number 26E055000

Grote

Grote Marker Lights

Exterior lighting defect

NHTSA, , Part, NHTSA campaign number 26E054000

Odyne

Odyne Systems Hybrid System Batteries

Electrical system defect

NHTSA, , Part

The Blood Connection Red Blood Cells, Leukocytes Reduced

Quality testing problem

Low risk, FDA, , Ended, Hospital use

8 recalls that day

Salata Jalapeño Avocado Dressing

Salmonella

High risk, FDA,

Vitasia Asian Style Wok Spice Mix

Salmonella

High risk, FDA,

Schwarzkopf Professional Osis Grip Mousse

Packaging defect

Moderate risk, FDA,

Frankie's Organic Plant-Based Puffs Vegan Cheddar

Undeclared milk

High risk, FDA, , Ended

Straumann Bone Level Tapered (BLT) Implant

Labeling error

Moderate risk, FDA,

Waldemar Link Endo-Model Tibial Plateau Replacement Sets

Device defect

Moderate risk, FDA,

Baxter Duo-Vent Solution Set and Male Luer Lock Adapter

Device defect

High risk, FDA,

Spectra Medical Devices Sodium Chloride Injection

Sterility problem

High risk, FDA,

15 recalls that day

Tyenne (Tocilizumab-Aazg) Injection

Foreign object

High risk, FDA,

Philips Azurion

Software defect

Moderate risk, FDA,

Philips Azurion Interventional Fluoroscopic X-Ray Systems

Software defect

Moderate risk, FDA,

Hoxworth Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99417

Straumann GM Helix Dental Implants

Labeling error

Moderate risk, FDA,

Philips Allura Xper FD Interventional Fluoroscopic X-Ray Systems

Software defect

Moderate risk, FDA,

Terumo Glidesheath Slender A-Kit

Device defect

Moderate risk, FDA,

Blue Bird

Blue Bird Vision Transit Bus (2023-2027)

Electrical system defect

NHTSA,

Blue Bird

Blue Bird Vision School Bus (Electric)

Electrical system defect

NHTSA,

Marion

Marion Body Works 2025 Pumper Fire Engines

Vehicle equipment defect

NHTSA,

Thomas Built Buses

Thomas Built Buses Saf-T-Liner C2 School Buses

Fuel system defect

NHTSA,

Thomas Built Buses

Thomas Built Buses Saf-T-Liner C2 Transit Buses

Fuel system defect

NHTSA,

LifeShare Blood Center Red Blood Cells, Leukocytes Reduced

Donor screening problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99416

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