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Momcozy

Shenzhen Lutejiacheng Supply Chain Management Co., Ltd. · Model A1-IR-D · UDI-DI 06975983271065

ISA
10
510(k) clearances
163
Adverse events (4 deaths)
10
Recalls
791
Facilities

Recalls

DateFirmReason
2026-06-23Therabody, IncCharging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has received reports alleging the prod
2025-10-09Pivotal Health Solutions, Inc.The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to s
2025-10-09Pivotal Health Solutions, Inc.The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to s
2025-04-09Richard Wolf GmbHThe high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell.
2020-12-15Wahl Clipper CorpThe connection between the massager and heat element can overheat causing smoke or spark, which may pose a fire hazard
2011-08-30King InternationalThe covered rotating mechanism can catch on user's clothing, jewelry (e.g. necklace), and hair. There have been reports of one death and a strangulation associated with using the
2008-06-18Sybaritic, IncMisbranded and sale without pre-market notification.
2005-11-01Wahl Clipper CorpThe massager may develop a crack in the cord insulation where it exits out of the strain relief. A crack in the insulation may expose live conductors resulting in a possible elect
2005-11-01Wahl Clipper CorpThe massager may develop a crack in the cord insulation where it exits out of the strain relief. A crack in the insulation may expose live conductors resulting in a possible elect
2004-12-10Wahl Clipper CorpThe housing of the massager's heating applicator attachment may crack during use. If the plastic housing cracks and breaks it could expose the user to live electrical connections

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.