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Zhejiang Luyao Electronics Technology Co., Ltd. Pingyang County Wenzhou China

Zhejiang Luyao Electronics Technology Co., Ltd. Pingyang County Wenzhou China Recalls

All product recalls associated with Zhejiang Luyao Electronics Technology Co., Ltd. Pingyang County Wenzhou China.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 2041–2060 of 37661 recalls

Homedics Leg Massager (Luyao Electronics) – packaging error (2025)

Regulatory documentation error and misleading color packaging claim.

Low

FDAJan 17, 2025Nationwide• Zhejiang Luyao Electronics Technology Co., Ltd. Pingyang County Wenzhou China

Timken Wheel Hub Bearing (Timken) – oil plug issue (2025)

Timken Company (Timken) is recalling certain model TP1HUBA wheel hub bearings sold on or before December 31, 2024. The oil plug port may be threaded incorrectly, allowing oil to leak.

High

NHTSAJan 17, 2025Nationwide• TIMKEN

Forest River Ahara Trailer (Forest River) – water heater venting (2025)

Forest River, Inc. (Forest River) is recalling certain 2025 East to West Ahara fifth wheel trailers. The water heater exhaust is ventilated directly under the slideroom, allowing carbon monoxide to enter the vehicle.

Very High

1...101 102103104 105...1884

Page 103 of 1884Next

NHTSA

Jan 17, 2025

Nationwide

• FOREST RIVER

Biostime Kids Calm & Sleep Fruity Bites (H&H) – Foreign Metal Objects (2025)

Due to foreign object: metal balls (tiny non-magnetic metal balls measuring less than 2mm inside the gummies) intended for children

Class IIModerate

FDAJan 17, 2025CA, IL, IN +1 more• Health and Happiness (H&H) LLC.

Badger Sunscreen SPF 50 (Badger) – Labeling Omission (2025)

Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.

Class IIILow

FDAJan 17, 2025Nationwide• The W.S. Badger Company, Inc.

Quantum Perfusion Blood Pump (Spectrum) – fluid leakage (2025)

Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.

Moderate

FDAJan 16, 2025Nationwide• Spectrum Medical Inc

Peterbilt 535 (Peterbilt) – accelerator pedal issue (2025)

PACCAR Incorporated (PACCAR) is recalling certain 2023-2024 Peterbilt 535, 536, 537, 548, 2023-2024 Kenworth T280, T380, T480, and 2024 Kenworth T180 trucks. The throttle pedal assembly may contain an oversized magnet carrier, slowing the responsiveness or causing the pedal to stick.

High

NHTSAJan 16, 2025Nationwide• PETERBILT

RayStation Planning System (RaySearch) – density uncertainty (2025)

Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a HU-to-mass density CT calibration curve used in RayStation version 4.5 to 2024B including some service packs.

Moderate

FDAJan 16, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Ranger XD 1500 ROVs (Polaris) – Vehicle Safety Issue (2025)

This recall involves certain VINs of Polaris Model Year 2024-2025 RANGER XD 1500 and RANGER CREW XD 1500 ROVs. The recalled ROVs were sold in camouflage, red, silver and titanium colors. The vehicles were sold in three- and six-seat configurations and have "POLARIS" stamped on the front grille. The VIN is printed on a portion of the left rear frame (on the driver's side of the vehicle) under the cargo box. In addition, this recall involves doors purchased as an accessory with part numbers 2212292, 2212291, 2638498, 2638499, 2638500, 2638501, 2889075 or 2889076. All accessory doors purchased for Polaris Model Year 2024-2025 RANGER XD 1500 and RANGER CREW XD 1500 ROVs prior to November 11, 2024 are affected by this recall.

High

CPSCJan 16, 2025Nationwide• Polaris Industries Inc., of Medina, Minnesota

IntelliVue Patient Monitor (Philips) – Alarm Failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

High

FDAJan 15, 2025FL, NC• Philips North America Llc

DeRoyal AMG Suction Connector (DeRoyal) – Seal Integrity (2025)

The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.

Moderate

FDAJan 15, 2025AZ, AR, GA +18 more• DeRoyal Industries Inc

IntelliBridge EC10 Module (Philips) – alarm failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

High

FDAJan 15, 2025FL, NC• Philips North America Llc

Sevoflurane Vaporizer (Getinge) – chemical degradation (2025)

Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.

High

FDAJan 15, 2025CT, KY• Getinge Usa Sales Inc

IntelliVue Patient Monitor (Philips) – alarm failure (2025)

Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.

High

FDAJan 15, 2025FL, NC• Philips North America Llc