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Week of July 6–12, 2026

The week in recalls

Heart pump kits and sterile trays led the recalls, with leaks and sterility gaps that matter to patients and clinicians. Cars and a few foods filled out the list.

Recall CanaryUpdated

Let's look at what got recalled this week. There were 76 recalls in all, and medical devices made up the largest share of them. The ones that matter most involve heart pumps and the kits used to place them, so let's start there.

Abiomed recalled its Impella heart pumps and introducer kits because the introducer sheaths can leak from under the sheath cap and along the hub score lines. The company says the problem is not something you can see just by looking at the device, and every pump set includes one of these introducers. Oscor separately recalled its Abiomed Impella introducer kits for the same kind of leaking from the sidearm and hub area. Both are high risk. If you work with these devices, check the lot numbers and follow the instructions that came with the recall notice.

Argon Medical recalled cardiovascular and biopsy trays that contain lidocaine ampules which did not meet release criteria for sterility. That means the ampules may not be sterile, so there is a chance of infection. These trays went out nationwide, and they are also high risk.

BMW recalled its BMW 330e iPerformance (2016-2018), BMW 530e iPerformance (2018-2020) because the engine starter relay can corrode and short circuit, which could start a fire. The notice says to park outside, away from your home, until the fix is done. Subaru also recalled its Subaru Ascent (2019-2026), Subaru Crosstrek Hybrid (2026) with an incorrect weight rating on the label, which could lead to overloading. You can find every recall, with lot numbers and contact details, in the full list below.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 76 recalls listed by then.

All 76 recalls this week

Newest first

Recalls the agencies dated Jul 6 to 12. 30 arrived after the week ended. How this list is made

10 recalls that day

Boston Scientific Rapid Refill Continuous Injection System

Device defect

Moderate risk, FDA,

ICU Medical Plum Duo Infusion and Solo Precision IV Pump

Device defect

Moderate risk, FDA,

Oscor Abiomed Impella Introducer Kits

Manufacturing problem

High risk, FDA,

Argon Medical Devices Cardiovascular and Biopsy Trays

Sterility problem

High risk, FDA,

Abiomed Impella Heart Pumps and Introducer Kits

Manufacturing problem

High risk, FDA,

Olympus Evacuators

Sterility problem

Moderate risk, FDA,

NAPA

NAPA Steering Inner Tie Rod Ends

Steering defect

NHTSA, , Part

Grand Design

Grand Design Lineage (2026-2027)

Vehicle equipment defect

NHTSA,

Zoox

Zoox Automated Driving Systems

Electrical system defect

NHTSA, , Part

Intuitive Surgical da Vinci SP Instrument Arm Drape

Device defect

Moderate risk, FDA,

18 recalls that day

Insignia Gas Ranges

Fire hazard

CPSC,

BBRKIN and MouTec Biometric Gun Safes

Injury hazard

CPSC,

Cuisinart Propel+ Four Burner 3-in-1 Gas Grill with Pizza Oven

Cut hazard

CPSC,

Flaunt MagSafe Battery Chargers

Fire hazard

CPSC,

24V and 48V Kobalt Yard Power Tools with USB-C Batteries

Fire hazard

CPSC,

Moodooy Adult Portable Bed Rails

Entrapment hazard

CPSC,

WonderStone Infant Walkers

Fall hazard

CPSC,

Versius Surgical System

Software defect

Moderate risk, FDA,

Think Surgical TMINI Femur and Tibia Tracking Arrays

Device defect

Moderate risk, FDA,

Vitek 2 AST-N447 Test Kit

Device defect

Moderate risk, FDA,

OmniTract Surgical Retractor System

Sterility problem

Moderate risk, FDA,

GSP Neonatal GALT Kit

Device defect

Moderate risk, FDA,

Elekta Brachytherapy Applicators

Device defect

Moderate risk, FDA,

Volvo

Volvo VAH (2026), Volvo VHD (2026), Volvo VN (2026), and 2 more

Steering defect

NHTSA,

Mississippi Blood Services Apheresis Platelets, Leukocytes Reduced, Pathogen Reduced

Moderate risk, FDA, , Ended, Hospital use

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99180

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99179

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99178

20 recalls that day

Somerset Therapeutics Pemetrexed, Bortezomib and Azacitidine for Injection

Manufacturing problem

Moderate risk, FDA,

KL Owen Custom Orthodontic Solution

Device defect

Moderate risk, FDA,

Atellica CH Enzymatic Hemoglobin A1c (A1c_E)

Device defect

Moderate risk, FDA,

MiniMed 780G Insulin Pump

Software defect

Moderate risk, FDA,

Medline Convenience Kits

Device defect

Moderate risk, FDA,

Gasco and Drogueria San Juan Isopropyl Alcohol

Wrong drug strength

Moderate risk, FDA,

Fresenius Medical Care 5008X Blood Tubing Sets

Device defect

Moderate risk, FDA,

Boston Scientific Neuromodulation Intracept Access Instruments

Sterility problem

Moderate risk, FDA,

Encore Medical EMPOWR 3D Knee Implants

Packaging defect

Moderate risk, FDA,

BMW

BMW 330e iPerformance (2016-2018), BMW 530e iPerformance (2018-2020), and 2 more

Fire risk when parked

High risk, NHTSA,

Husqvarna

GasGas ES 350 (2024), GasGas ES 500 (2024), Husqvarna FE 350S (2022-2024), and Husqvarna FE 501S (2022-2024)

Brake defect

NHTSA,

Peterbilt

Kenworth T680 (2027) and Peterbilt 579 (2026-2027)

Brake defect

NHTSA,

Forest River

Forest River Wildwood and Salem Travel Trailers

Vehicle equipment defect

NHTSA,

Toyota

Lexus TX, Lexus TX Hybrid, Lexus TX Plug-In Hybrid, and 2 more (2026)

Transmission or drivetrain defect

NHTSA,

Utilimaster

Utilimaster Velocity (2016, 2019, 2021)

Exterior lighting defect

NHTSA,

BMW

BMW 2 Series, 3 Series, 4 Series, 5 Series, X3, X4, Z4 and Toyota Supra Vehicles

Electrical system defect

NHTSA,

LifeServe Blood Center Apheresis Red Blood Cells, Leukocytes Reduced

Quality testing problem

Low risk, FDA, , Ended, Hospital use

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99177

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99175

Lifesouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99174

21 recalls that day

Vitalant Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use

Fresh to You Burger Chicken Fillet

Salmonella

High risk, FDA, , Ended

Trafa Pharmaceuticals Organic Moringa Leaf Powder

Salmonella

High risk, FDA,

QuVa Pharma Methohexital Sodium

Drug impurity

Moderate risk, FDA,

Giant Vanilla Dessert Shells

Undeclared soy

Moderate risk, FDA, , Ended

Wondermade Alabama Banana Pudding Marshmallows

Foreign object

Moderate risk, FDA, , Ended

Medline Remedy Specialized Silicone Cream (Hydraguard-D)

Quality testing problem

Moderate risk, FDA,

Shimoga Chemicals Clomiphene Citrate Active Pharmaceutical Ingredient

Manufacturing problem

Moderate risk, FDA,

Beauty Pie Super Healthy Hair Blow Dry Spray

Contamination

Moderate risk, FDA,

Avet Methohexital Sodium for Injection

Drug impurity

Moderate risk, FDA,

ConvaTec Aquacel Ag Surgical SP

Quality testing problem

Moderate risk, FDA,

Wise Onion Rings

Undeclared color or additive

Moderate risk, FDA, , Ended

Olympus Single Use Distal Cover

Device defect

Moderate risk, FDA,

Braun

Braun Chevrolet Traverse Vehicles

Fuel system defect

NHTSA,

Kenway

Kenway 12V LED Towing Light Kits and 12V Submersible Lights

Exterior lighting defect

NHTSA, , Part

Subaru

Subaru Ascent (2019-2026), Subaru Crosstrek Hybrid (2026), Subaru Forester (2025-2026), and 1 more

Vehicle equipment defect

NHTSA,

Wabash

Wabash Econex Refrigerated Body Vehicles

Vehicle structure defect

NHTSA,

Tesla

Tesla Model 3 (2024) and Tesla Model Y (2026)

Air bag defect

NHTSA,

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99173

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99172

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99171

7 recalls that day

Fayus Ola-Ola Pounded Yam

Undeclared milk

High risk, FDA,

Adams Extract & Spice Seasonings and Mixes

Undeclared sesame

High risk, FDA, , Ended

American Seating

Prime-Time Ford Med Transit Vans With Q'Straint Max Wheelchair Retractors

Mobility equipment defect

NHTSA, , Part

Toyota

Toyota Tundra (2026) — Equipment

Vehicle equipment defect

NHTSA,

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced, Irradiated

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99163

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99161

LifeSouth Community Blood Centers Apheresis Platelets, Leukocytes Reduced

Quality testing problem

Moderate risk, FDA, , Ended, Hospital use, FDA event number 99160

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