Latest Product Recalls Today

Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the patient's mouth there is an increased risk of fractures under functional stress.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Sterile anchors my lack sterility assurance.

Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuration (128 or 256 channels) running firmware version 2022.02 were displayed with a shift of 1 second between the 64channels blocks. In rare circumstances, a fixed 1-second temporal delay may appear between two 64-channel modules with firmware 2021.02, 2022.01 or 2022.02 in a multi-module SEEG configuration, potentially leading to misinterpretation of results.

Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

Reusable electrodes may not meet expected performance levels.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product correctly identifies the product code and the solution contained in the bag. In the event the incorrect GTIN labeling is used as the singular source for product identification, unrecognized use of a potassium solution with a concentration differing from the prescription may result.

GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Storyteller Overland, LLC (Storyteller) is recalling certain 2024-2026 GXV Hilt vehicles. The secondary alternator pulley may fail, resulting in a loss of power brakes and power steering. An unexpected loss of power brakes increases the distance required to stop. A loss of power steering increases the amount of effort needed to control the vehicle. Both situations may increase the risk of a crash.

Forest River, Inc. (Forest River) is recalling certain 2023-2024 XLR Toy Hauler recreational trailers. The listed Gross Vehicle Weight Rating (GVWR) exceeds the weight rating on the upper deck chassis. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims-Other than Passenger Cars." Referencing the incorrect GVWR may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

Wabash National Corporation (Wabash) is recalling certain 2027 Wabash van trailers. The bumper tube bolts may have been improperly tightened, reducing the protection provided by the rear impact guard. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 223, "Rear Impact Guards." An improperly installed guard may not sufficiently protect a following vehicle, increasing the risk of injury during a rear end crash.

Waymo LLC (Waymo) is recalling certain 5th Generation Automated Driving Systems (ADS). The software may allow the vehicle to enter a closed freeway construction zone and continue driving at speed. Driving through a closed construction zone increases the risk of a crash.

Editor’s Note: June 12, 2026 – This release has been revised to reflect the accurate BEST BY date for the first product listed. The correct date is 13 DEC 2026, replacing the incorrect date of 23 DEC 2026. WASHINGTON, May 31, 2026 – Synear Foods USA, LLC, a Chatsworth, Calif. establishment, is recalling approximately 71,603 pounds of frozen not-ready-to-eat (NRTE) pork and crab soup dumpling products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains peanut, a known allergen, which is not declared on the product label. The frozen NRTE pork and crab soup dumpling products were produced between October 15, 2025, and February 23, 2026. The following products are subject to recall [ view labels ]: 13.23-oz. plastic bag packages containing “Synear SUPREME SOUP DUMPLING PORK & CRAB” and “BEST BY” dates 15 OCT 2026, 10 NOV 2026, 13 DEC 2026, 26 JAN 2027, or 23 FEB 2027. 375-g. plastic bag packages containing “Synear SUPREME SOUP DUMPLING DUMPLINGS À LA SOUPE SUPRÊME PORK & CRAB PORC ET CRABE” with “Product of USA/Produit des E.-U” and best by dates 2026 OC 15 or 2027 JA 26. The products subject to recall bear establishment number “EST. 45942” inside the USDA mark of inspection. These items were shipped to retail locations in California, New Jersey, and Washington. These products were also exported to Canada. The problem was discovered by FSIS inspection personnel during a routine allergen verification task. FSIS personnel identified that the products were formulated with peanut oil, but peanuts were not declared on the finished product label. The establishment determined that a formulation change led to the mislabeling. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider. FSIS is concerned that some product may be in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls . Consumers and members of the media with questions about the recall can contact Judy Zhu, CEO, Synear Foods USA, LLC, at 818-341-3588 EXT. 101 or [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .

Winnebago Industries, Inc. (Winnebago) is recalling certain 2026-2027 Revel and Revel Sport recreational vehicles. The tire information label states an incorrect tire. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, "Tire Selection and Rims." Referencing the incorrect information could cause owners to install the wrong size replacement tires, increasing the risk of a crash.

Marion Body Works Inc. (Marion Body Works) is recalling certain Waltco MDV series liftgates installed on Morgan aluminum dry vans. The deck pins may break, resulting in the liftgate platform falling. A liftgate that falls unexpectedly increases the risk of injury.

Altec industries, Inc. is recalling certain 2014-2026 AT Series Aerial Device vehicles. The transmission park interlock may be missing, allowing the aerial device to operate while the chassis is not in park. An aerial device that operates while the vehicle is in gear or neutral can cause unexpected vehicle movement and increase the risk of injury.