79 recalls tagged with “mandatory standard violation”.
Kia America, Inc. recalled certain 2023-2025 K5 vehicles on April 7, 2027. The recall involves rear window trim pieces that may loosen and detach, creating a road hazard. Owners should contact Kia for inspection and potential replacement of affected parts.
ShymeryDirect LED Lights are recalled. The recall was issued on April 9, 2026. The recall involves 24 LED lights containing two CR2032 lithium coin batteries each. Packaging code X0037GYJYX is shown on the product. Consumers should stop using the lights and contact Shymeryrecall0402@outlook.com for a full refund.
Besslly recalled its CHD-014-2 Halloween Pumpkin Carving Kit sold on Amazon after the tea lights’ button-cell batteries pose an ingestion risk. The recall involves five tea lights with 15 button batteries and a set of carving tools, emoticon stickers, a handbag, and gloves, and it lacks the Reese’s Law warnings. Stop using the recalled kit now and email tingjmng@outlook.com to receive a fullrefund
SCUBAPRO recalled Monorail Weight Pockets for BCDs sold by retailers worldwide on 2026-04-09 after safety reviews identified a serious entrapment risk. The recall notes a potential for entrapment and drowning and cites missing warning labels. Consumers should stop using the recalled bed rails and contact SCUBAPRO for a full refund.
Maitys is recalling magnetic drinkware charms sold on Amazon in 400-piece sets. The magnets are loose and violate the mandatory standard for magnets. Consumers should stop using the recalled charms immediately and contact Maitys for a full refund.
ELENKER recalled three models of portable bed rails sold on Amazon by Fuzhou Shiahaha Cultural Industry Development. The rails can entrap users or create a gap with the mattress, posing a risk of suffocation and death, and they lack required hazard warnings. Consumers should stop using the rails immediately and contact the company for a full refund.
Goregent is recalling Goregent-branded infant walkers sold on Amazon. The recalled walkers can fit through a standard doorway and fail to stop at the edge of a step. Parents should stop using the recalled walkers immediately and contact Goregent Official Store for a full refund.
Aisstxoer adult bicycle helmets sold on Amazon by YXTDZ Store are being recalled. The helmets fail to meet mandatory safety standards for impact attenuation and stability, creating a serious head-injury risk. Stop using the recalled helmet now and contact YXTDZ Store for a full refund; destroy the helmet and email a photo to yxtdzamz@126.com.
Stoney Games recalled Kluster Fun Tabletop Magnet Chess Games on March 12, 2026, due to a serious ingestion hazard. The games contain loose, high-powered magnets that can be swallowed by children, posing a risk of severe injury or death. Consumers should immediately stop using the games and contact Stoney Games for replacement options.
ProRider recalled several models of bicycle helmets on March 12, 2026, due to a serious risk of head injury. The helmets do not meet mandatory safety standards and can fail in a crash. Consumers should stop using these helmets immediately and seek a refund.
Unique Brands Com recalled Forever 21 Kids Disney Mickey Mouse Pajama Pants on March 5, 2026. The pants pose a significant burn hazard due to flammability standards violations. Parents should stop using them immediately and seek a refund.
Philips Medical Systems Nederland B.V. recalled 345 Azurion 5 M12 X-ray systems distributed worldwide after reports that X-ray imaging may not start or may run intermittently when using the wired foot switch. The defect could affect imaging during patient care. Hospitals should stop using the device immediately and follow the recall instructions in the notification letter.
Philips recalls 298 Azurion 3 M12 X-ray imaging systems used by healthcare providers worldwide. The issue is that X-ray imaging may not start or may be intermittent when using the wired foot switch. Stop using the affected devices immediately and follow recall instructions from Philips.
Civco Medical Instruments recalled 10 eTRAX Needle Sensor 16G units for Aurora Trackers. An inspection and programming error could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.
Synthes bone taps recalled nationwide in the United States after a lot swap affected 33 units sold through multiple retailers. The defect is an incorrect thread caused by a lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8. Healthcare providers should stop using these devices immediately and follow recall instructions from Synthes.
Mentor Texas, LP is recalling Artoura Breast Tissue Expanders with infusion sets worldwide, including the United States and Canada. The infusion sets may contain dull or blunt needle tips that are difficult to advance or may break. Patients and healthcare providers should stop using the device and follow recall instructions.
Merit Medical Systems recalled 47,153 BioFlo DuraMax Catheters distributed worldwide through medical distributors after a design defect in the 16F dual-valved splittable sheath introducer may fail to split as intended. The defect can cause hemorrhage, foreign bodies, and delays in procedures. Clinicians and patients should stop using the device immediately and follow recall instructions from Merit
Burlington Medical recalled 402 Half Aprons sold worldwide after potential attenuation degradation. Attenuation material Xenolite 800 may degrade over time, reducing shielding lifespan. Patients and healthcare providers should stop using the aprons immediately and contact Burlington Medical for recall instructions.
Burlington Medical recalled 15,438 attenuation vests distributed worldwide after potential attenuation degradation over time. The vests use Xenolite 800 attenuation material and were produced between January 16, 2025 and January 21, 2026. Healthcare providers and patients should stop using the vest immediately and follow recall instructions.
Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.