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The Mochi Ice Cream Company recalled My Mochi Strawberry flavored non-dairy frozen dessert (7.5 oz containers, 6 pieces) because a foreign object was found inside a retail container. The affected product has lot number 041-26 with a best-by date of February 20, 2027.

Moderate·FDA·May 6, 2026·My Mochi

Ganesha Enterprises' KLG brand Kesar Mukhwas (a traditional Indian mouth freshener) contains undeclared food colorings—Yellow 6, Blue 1, and Yellow 5—plus an unapproved artificial dye called Acid Red 14. These were not listed on the package label. The product was distributed in California, Georgia, Illinois, New York, and Tennessee.

Moderate·FDA·May 6, 2026

Specially SELECTED brand Vanilla Creme Brulee dessert (3.6 oz) sold at Aldi may contain glass fragments. The product comes in a glass jar and affected units have a best-by date of 5/9/2026. About 2,869 cases were distributed to stores in New York, Indiana, Florida, Illinois, Virginia, Maryland, and Michigan.

Moderate·FDA·May 6, 2026·Specially Selected

Negita Shrimp Crackers (2.8 oz) contain FD&C Yellow 6, a food dye that is not listed on the package label. People with allergies or sensitivities to Yellow 6 could have a reaction if they consume this product without knowing the dye is present.

Moderate·FDA·May 6, 2026

Zonegoing is recalling three flavors of 52USA popping boba: strawberry, passion fruit and mango, all in 7 lb (3.2 kg) bags. The products contain food colors the FDA has not approved: tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6) and allura red (FD&C Red 40). The products were distributed in New York, and no injuries have been reported.

Moderate·FDA·May 6, 2026·52USA3 products

Schreiber Foods Inc. is recalling Einstein Bros Bagels Honey Almond Double-Whipped Shmear (labeled as Plain Whipped Cream Cheese Spread on the cup) because it contains almond that is not declared on the label. People with almond allergies who consume this product could have an allergic reaction.

Moderate·FDA·May 6, 2026

Winfield's Chocolate Bar recalled five dark chocolate products sold at its three Houston locations because the ingredient label failed to list milk, a major food allergen. People with milk allergies or sensitivities could have a serious allergic reaction if they eat these products. No illnesses have been reported so far.

Moderate·FDA·May 5, 2026

My Wife's Slaw is recalling Original and Jalapeno Heat flavored coleslaw sold in 8 oz and 16 oz glass mason jars because the products were made without proper inspection and safety verification. The coleslaw was produced between April 1 and April 28, 2026, and sold online nationwide. No illnesses have been reported so far.

Moderate·FDA·May 5, 2026

Giovanni Rana Rustic Beef Sauce & Creamy Burrata Cheese Ravioli (32-oz packages) sold at Costco in Maryland and New Jersey actually contain shrimp and lobster filling, which are not listed on the label. The mislabeling poses a serious risk to people with shellfish allergies. No illnesses have been reported so far.

Moderate·USDA·May 4, 2026·Giovanni Rana

Waymo's automated driving software in certain 5th and 6th generation systems may allow vehicles to drive onto flooded roadways, which can cause loss of control and increase crash risk. Waymo has already applied a temporary fix to all 3,791 affected vehicles by April 20, 2026, adding weather constraints and updating maps to avoid standing water.

Moderate·NHTSA·May 1, 2026

A loose screw on the Acer AES015 folding electric scooter can cause the front tube to collapse unexpectedly while riding, creating a fall hazard. The scooters were sold online and in stores between June 2023 and February 2026. One injury has been reported internationally.

Moderate·CPSC·Apr 30, 2026

Marquez Brothers is recalling three horchata products: two EL MEXICANO instant horchata drinks (14 oz and 12 oz agua fresca de horchata) and bulk Horchata Powder sold in 25-pound cases. The products may contain milk that is not listed on the label, which is a risk for people with milk allergies. The products were distributed in 30 U.S. states and to Canada and Japan.

Moderate·FDA·Apr 29, 20263 products

Summit Import Corporation's spice powder (4 oz, plastic bag) was found to contain lead levels higher than New York State standards. About 20 cases of the product were distributed across eight states.

Moderate·FDA·Apr 29, 2026

Ethnic Foods is recalling two Bombay Kitchen products, Tikka Sev and Punjabi Mix, both 9 oz (255 g) packages. The labels do not list the colors FD&C Yellow #6 and FD&C Red #40, which the products contain, and the products were distributed in New Jersey. No injuries have been reported.

Moderate·FDA·Apr 29, 20262 products

Mondelez Global found hard corn starch lumps in Chips Ahoy Baked Bites Brookie snack cakes sold in multiple states. The affected products are the 22.4 oz carton (2.8 oz pouch) and 7.7 oz carton (1.4 oz pouch) with specific best-by dates in May 2026.

Moderate·FDA·Apr 29, 2026·CHIPS AHOY!

Teva Pharmaceuticals is recalling specific lots of Claravis (isotretinoin) 10 mg capsules because they contain higher-than-allowed levels of tretinoin, a related chemical impurity. The affected lots are 100067507 and 100067508, which expire on July 31, 2026. No injuries have been reported so far.

Moderate·FDA·Apr 29, 2026

General Motors is recalling certain containers of ACDelco GMW DOT 3 brake and clutch fluid (lot #01977 091222) because the fluid may contain visible sediment. Sediment in brake fluid can reduce braking performance and increase the risk of a crash.

Moderate·NHTSA·Apr 23, 2026

Philips has identified three software issues in the Spectral CT on Rails Model 728334 that may affect scan operations. The gantry (rotating scanner) may not move to the correct position after pressing start; a required confirmation message may not appear; and a menu option may become unavailable during brain imaging setup. Three systems worldwide are affected.

Moderate·FDA·Apr 22, 2026

Medline distributed one lot of CENTURION Circumcision Kits (lot number 25KLA002) without completing the required sterilization process. This means the kits are not sterile and could pose an infection risk if used. The affected kits were distributed in South Carolina.

Moderate·FDA·Apr 22, 2026

The Gentuity HF-OCT Imaging System may display repeated image frames during a pullback procedure when used with certain catheters, which could affect the accuracy of length measurements. This issue affects specific software versions (21.11 to 23.3.13) paired with Vis-Rx and Vis-Rx Prime catheters. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·Gentuity

The centrifuge bowl on certain Cellex Photopheresis System kits may be difficult to install properly onto its holder. If not installed correctly, the bowl can break during use, which could delay patient treatment and cause blood loss.

Moderate·FDA·Apr 22, 2026·Theranos

Clariance-SAS is recalling multiple lots of Elegance Anterior Cervical Plates (used in neck spine surgery) due to burrs found on some finished plates. The burrs are sharp edges that could cause injury during or after implantation. No injuries have been reported so far.

Moderate·FDA·Apr 22, 2026·Clariance

Integra LifeSciences is recalling five sizes of Cytal Wound Matrix and Cytal Burn Matrix products because an increased rate of endotoxin test results fell outside acceptable limits. The recall covers 879 units distributed across many US states. No injuries have been reported.

Moderate·FDA·Apr 22, 20265 products

3B Medical distributed 2 units of the React Health PHOENIX 5L Oxygen Concentrator that did not meet the company's internal quality standards. The devices were distributed in New York. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·3B Medical

Siemens has recalled certain ARTIS Pheno VE30A and VE40A imaging systems used in hospitals and medical facilities. During 3D imaging procedures, these systems may produce images with uneven brightness, potentially leading to less accurate reconstructions and unintended low-dose radiation exposure to patients.

Moderate·FDA·Apr 22, 2026

Wilson-Cook Medical is recalling Instinct Plus Endoscopic Clipping Devices (model G58010) due to increased complaints about potential device malfunction during use. The recall affects units manufactured between September 2, 2023 and April 20, 2025 and distributed worldwide. No injuries have been reported.

Moderate·FDA·Apr 22, 2026

The LinkBio CORE Workstation, part of the CORE Shoulder System, may show an incorrect Planning Date when you view cases in the Start Case menu. This could lead to confusion about case timing. Five units are affected across Alabama, Florida, and Kansas.

Moderate·FDA·Apr 22, 2026·Linkbio

Remel's Yeastone Broth (11ML, 10/BOX, model YY3462) may give wrong results when labs use it to test how fungi respond to antifungal medicines. If a lab doesn't catch the bad result during its own quality checks, doctors might delay treatment or switch to a different antifungal drug unnecessarily.

Moderate·FDA·Apr 22, 2026

Philips AneurysmFlow is software used by doctors to help evaluate aneurysm treatment with flow diverter stents. The software's Mean Aneurysm Flow Amplitude (MAFA) ratio does not reliably predict whether the aneurysm is successfully closed, but doctors may be using it to make treatment decisions based on the user manual.

Moderate·FDA·Apr 22, 2026

Pure Palm Medjool Dates (16 oz, UPC 852160007005, Lot PP0576D1) are labeled as regular date bites but actually contain coconut coating. The mislabeling means customers with coconut allergies may unknowingly consume the product. Approximately 50 cases were distributed to retailers across Delaware, Pennsylvania, New Jersey, Maryland, and New York.

Moderate·FDA·Apr 22, 2026