185 recalls tagged with “federal law violation”.
Siemens Medical Solutions USA recalled one MAMMOMAT Fusion operator table on October 24, 2025. The table was sold with a bus-installation kit but is intended for stationary use only. This recall affects distribution in Arkansas, California, New York, and internationally in Australia, Canada, and India.
Mindray DS USA, Inc. recalled 54 units of the Isoflurane V90 Electronic Vaporizer on October 20, 2025. The recall stems from a potential anesthesia leakage issue that poses serious health risks. Affected devices were distributed in the U.S. and Canada.
VESTA.DS recalled VST-brand tankless water heaters on October 16, 2025. The recall affects multiple models due to a carbon monoxide poisoning hazard. Consumers should stop using the heaters immediately.
DermaSensor recalled 343 diagnostic devices on October 13, 2025, due to a risk of incorrect results. The recall affects nine units specifically identified for failing to meet specifications. This issue could delay patient referrals for necessary treatment.
STAQ Pharma Inc. recalled Hydromorphone HCL PF injections on October 9, 2025, due to incorrect or missing lot and expiration dates. The recall affects products distributed nationwide across the U.S. Healthcare providers and consumers must immediately cease using the affected medication.
Volkswagen recalled certain 2025 ID. Buzz vehicles on October 4, 2025. The brake system warning light may display incorrect symbols and colors. This defect increases the risk of a crash.
In Motion Design recalled Evermore Surprise Eggs on October 2, 2025. The toys contain lead levels exceeding federal limits, posing serious health risks to children. Consumers should stop using the eggs and seek refunds immediately.
Gunaito recalled 10,000 dressers on October 2, 2025, due to serious tip-over risks. The recalled dressers can cause injuries or death to children if not anchored to the wall. Consumers should stop using them immediately and seek a refund.
Persilux recalled zebra blinds on September 25, 2025, due to strangulation and entanglement hazards. The recalled blinds pose a serious risk of injury or death to children. Consumers should stop using the blinds immediately and contact Persilux for a repair kit.
Becton Dickinson & Co. recalled 38 units of BD Veritor Connect Software on September 23, 2025. Unauthorized access to product service credentials may compromise data confidentiality and integrity. Users must stop using the software immediately and follow recall instructions.
Becton Dickinson & Co. recalled 1,086 units of its BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a risk to data security. Affected systems include the BACTEC 9120 with catalog numbers 445570 and 445702.
ARVIS recalled 21 units of its Shoulder Surgical Navigation Software on September 19, 2025. A complaint identified issues that may cause implant malalignment and decreased range of motion. Healthcare providers and patients must stop using the software immediately.
LXDHSTRA recalled baby loungers on September 18, 2025, due to suffocation and fall hazards. The loungers violate federal safety standards for infant sleep products. Consumers must stop using them immediately and return them for a full refund.
EnHomee recalled its Fabric 13-Drawer Dressers on September 18, 2025. The dressers pose a serious tip-over risk if not anchored to a wall. This recall affects an unspecified number of units sold by EnHomee Direct.
GE Medical Systems recalled 37 LOGIQ P9 ultrasound systems on September 18, 2025. The devices may display inaccurate liver steatosis data, risking inappropriate clinical decisions. Healthcare providers must stop using the devices immediately and follow recall instructions.
Cook Medical recalled 695 Zenith Alpha 2 Thoracic Endovascular Grafts on September 18, 2025. The recall follows reports that PTFE coating scrapings could cause intravascular embolization during deployment. Patients and healthcare providers must stop using the device immediately.
GE HealthCare recalled 37 nuclear medicine gamma cameras on September 12, 2025. The recall follows concerns that inadequate detector support during transport could lead to life-threatening falls. The affected systems are past the End of Guaranteed Service and pose serious risks to patients and healthcare providers.
Major Pharmaceuticals recalled 866 blister packs of Chlorpromazine Hydrochloride Tablets on September 12, 2025. The recall follows the detection of N-Nitroso Desmethyl Chlorpromazine above safe limits. The affected products were distributed nationwide and are classified as a Class II hazard.
GE HealthCare recalled 11 Cardial nuclear medicine gamma cameras on September 12, 2025. The recall follows concerns over inadequate detector support potentially leading to life-threatening falls. The affected systems were transported without proper safeguards, compromising safety.
Unique Pharmaceuticals Labs recalled 9,936 bottles of Cetirizine Hydrochloride Tablets on September 12, 2025. The tablets were imprinted with the wrong ID, posing a potential health risk. Consumers should stop using the product immediately and seek guidance from healthcare providers.