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Week of April 27–May 3, 2026

The week in recalls

Infant formula and a surgical stapler reload topped the safety notices, while a seasoning and a hot cocoa mix carried contamination worries. A carmaker's blank dashboard also earned a place on the list.

Recall CanaryUpdated

Time for this week's recall roundup. There were 78 recalls listed, and most were medical devices. The ones that matter most involve an infant formula, a surgical stapler reload, and a seasoning. Let's start with the formula.

The a2 Milk Company recalled A2 Platinum Premium Infant Formula Milk-Based Powder with Iron because it may be contaminated with cereulide toxin, which can cause gastrointestinal illness in infants. This is a high risk recall, and the product was sold nationwide. If you have this formula, do not feed it to your baby. Check the package and return it to where you bought it or throw it away.

Cook Incorporated recalled Cook Centimeter Sizing Catheters because marker bands may crack or break. The broken pieces could cause vessel injury or make a procedure take longer. If you work in a cath lab, check your stock. Also, Intuitive Surgical recalled Intuitive 8 mm SureForm 30 Gray Reloads because they may produce an incomplete staple line. Surgeons and hospital staff should set these aside.

In food, Pork King Good Onion & Sour Cream Seasoning may be contaminated with Salmonella. The seasoning was made with milk powder that was already recalled for the same reason. It was sold in 26 states. If you have it, throw it out. Ghirardelli also recalled Ghirardelli Frappe Mixes, Sweet Ground Powders and Hot Cocoa Mix for possible Salmonella contamination. That recall covers 27 states. Check your pantry and do not use these products. That is a lot to keep track of, but checking your kitchen and your medicine cabinet is a good start. For the full list of this week's recalls, see below.

Written by Recall Canary from the agencies’ records on .

What changed

: First written on November 4 from the 78 recalls listed by then.

All 78 recalls this week

Newest first

Recalls the agencies dated Apr 27 to May 3. 15 arrived after the week ended. How this list is made

1 recall that day

A2 Platinum Premium Infant Formula Milk-Based Powder with Iron

Contamination

High risk, FDA, , Ended

17 recalls that day

Second Nature Keto Crunch Smart Mix

Undeclared tree nut

Moderate risk, FDA, , Ended

Unichem busPIRone Hydrochloride Tablets

Wrong drug strength

Low risk, FDA,

Spacelabs Ultraview SL Command Module

Manufacturing problem

Moderate risk, FDA,

Centinel Spine Prodisc C SK Total Cervical Disc Replacements

Labeling error

Moderate risk, FDA,

Halyard Cardiac Cath and Cath Lab Kits

Device defect

High risk, FDA,

Cook Centimeter Sizing Catheters

Device defect

High risk, FDA,

Boston Scientific LUX-Dx II Arrhythmia Detectors and Alarms

Software defect

Moderate risk, FDA,

Erbe ERBEFLO CleverCap CO2 Tubing and Cap Sets

Device defect

Moderate risk, FDA,

Da Vinci X, Xi Surgical System

Device defect

Moderate risk, FDA,

VOCSN V+Pro Package

Device defect

High risk, FDA,

Intuitive 8 mm SureForm 30 Gray Reloads

Device defect

High risk, FDA,

Mercedes-Benz

Mercedes-Benz AMG GT, C-Class, E-Class, SL, CLE, and GLC Vehicles

Electrical system defect

NHTSA,

Ram

Ram ProMaster (2026)

Seat defect

NHTSA,

New Flyer

New Flyer 2022 XE40 Transit Buses

Electrical system defect

NHTSA,

Waymo

Waymo Automated Driving Systems

Electrical system defect

NHTSA, , Part

GELLEN Time to Shine Nail Removal Kit

Chemical contamination

Moderate risk, FDA,

25 recalls that day

Richelieu Foods Meat and Poultry Products

Salmonella

FSIS,

My Mochi Strawberry Flavored Non-Dairy Frozen Dessert

Foreign object

Moderate risk, FDA, , Ended

Calypso Tropic Tango Lemonade

Undeclared color or additive

Moderate risk, FDA, , Ended

Ganesha Enterprises KLG Kesar Mukhwas

Undeclared color or additive

Moderate risk, FDA, , Ended

CVS Pharmacy Lidocaine Wound Gel

Quality testing problem

Low risk, FDA,

Medline and Centurion Medical Convenience Kits

Sterility problem

Moderate risk, FDA,

Medline Neuro Sponges

Quality testing problem

Moderate risk, FDA,

Hepo Adult Portable Bed Rails

Entrapment hazard

CPSC,

Honda Off-Road Motorcycles

Crash hazard

CPSC,

Afrin Original Nasal Spray Travel Size Bottles

Poisoning hazard

CPSC,

Malker Bicycle Light Sets

Swallowing hazard

CPSC,

Earthtec Pool Drain Covers

Entrapment hazard

CPSC,

Build-A-Bear Workshop Heartwarming Hugs Bears

Choking hazard

CPSC,

UHOMEPRO 5-Drawer Dressers

Tip-over hazard

CPSC,

DGIVOVO US Electric Pressure Washers

Electric shock hazard

CPSC,

Qumeney Bicycle Light Sets

Swallowing hazard

CPSC,

Thermos Food Jars and Beverage Bottles

Impact hazard

CPSC,

Segmart 4-Drawer Dressers

Tip-over hazard

CPSC,

Grand Design

Grand Design Lineage (2025-2026)

Seat defect

NHTSA, , NHTSA campaign number 26V277000

Grand Design

Grand Design Lineage (2025-2026)

Vehicle equipment defect

NHTSA, , NHTSA campaign number 26V276000

Nova Bus

Nova Bus LFS (2022-2025)

Electrical system defect

NHTSA,

18 recalls that day

Pork King Good Onion & Sour Cream Seasoning

Salmonella

High risk, FDA,

Hikma Pharmaceuticals Alendronate Sodium Oral Solution

Quality testing problem

Moderate risk, FDA,

North American Rescue AIDBAG First Aid Kits

Software defect

High risk, FDA,

Immuno-Mycologics Myco DDR Trident Neutralization Buffer B

Contamination

Moderate risk, FDA,

Depuy Synthes Attune Revision Hinge Femoral

Sterility problem

Moderate risk, FDA,

Siemens Epoc BGEM BUN Test Cards

Device defect

Moderate risk, FDA,

Straumann N!Ce Full-Arch Restorations

Device defect

Moderate risk, FDA,

Becton Dickinson BD GasPak EZ CO2 and Campy Pouch Systems

Device defect

Moderate risk, FDA,

Merit Medical Systems Philips Bridge Prep Kit

Device defect

Moderate risk, FDA,

Abbott Point of Care i-STAT EG7+, EG6+, and G3+ Cartridges

Manufacturing problem

Moderate risk, FDA,

Leksell Vantage Arc System

Device defect

Moderate risk, FDA,

Heraeus PALAMIX Duo and Uno

Device defect

Low risk, FDA,

Beta Bionics iLet Bionic Pancreas

Software defect

Moderate risk, FDA,

Newmar

Newmar Freedom Aire (2026)

Vehicle structure defect

NHTSA, , NHTSA campaign number 26V272000

Solutions

Dorman Transmission Gearshift Cables

Transmission or drivetrain defect

NHTSA, , Part

Newmar

Newmar Freedom Aire (2026)

Vehicle equipment defect

NHTSA, , NHTSA campaign number 26V273000

Storyteller Overland

Storyteller Overland Stealth, Classic, and Beast Mode Vehicles

Engine defect

NHTSA,

12 recalls that day

B. Braun Lactated Ringer's Injection

Foreign object

High risk, FDA,

Optase Dry Eye Intense Drops (Glycerin 0.2%)

Sterility problem

Moderate risk, FDA,

iVIZIA Sterile Lubricant Eye Drops

Sterility problem

Moderate risk, FDA,

Negita Shrimp Crackers

Undeclared color or additive

Moderate risk, FDA,

American Regent Levocarnitine Injection

Labeling error

Low risk, FDA,

Specially Selected Vanilla Creme Brulee

Foreign object

Moderate risk, FDA, , Ended

Wells Pharma Phenylephrine, Fentanyl and Ketamine Injectable Solutions

Manufacturing problem

Moderate risk, FDA,

Jayco

Entegra Condor and Jayco Granite Ridge Motorhomes

Vehicle equipment defect

NHTSA,

Ford

Ford Ranger and Bronco Front Seats

Seat defect

NHTSA,

Lode King

Lode King SDF50-3, Lode King SDF53-3, and Lode King SDG53-3 (2019-2026)

Vehicle structure defect

NHTSA,

5 recalls that day

Philips MRI Systems with MR Elastography

Software defect

Moderate risk, FDA,

Hemu Trading Enoki Mushrooms

Listeria

High risk, FDA, , Ended

HiResolution Bionic Ear System M Zn-Air Battery Pak

Device defect

Moderate risk, FDA,

Proliance

Proliance High Voltage Batteries

Electrical system defect

NHTSA, , Part

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