Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.
Aspiration system, for endoscopic examination/treatment of urinary tract and kidney interior, to have labeling update adding additional instructions, for patients with high viscosity fluid in the kidney, not to continue providing fluid inflow in the presence of unresolved slow or absent fluid outflow because this can create intrarenal pressure imbalance, and lead to excessive intrarenal pressure.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Zhangzhou Jiesi Intelligent Technology Co. Ltd., of China
🏠 Consumer Products Class II - Moderate
The recalled dressers are unstable if they are not properly anchored to the wall, posing serious tip-over and entrapment hazards, and the two additional metal support legs also present tripping hazards. The dressers violate performance and warning label requirements of the STURDY Act.
Delweld Industries Corp., of Stoystown, Pennsylvania
🏠 Consumer Products Class II - Moderate
The recalled children's bunk beds violate the federal regulations for bunk beds because the spacing between the guardrail and end support and the spacing around the mattress supports are greater than allowed, posing entrapment and strangulation hazards to children.
The recalled jewelry-making kits contain a resin that, when liquid, can cause skin, eye and respiratory irritation or sensitization when inhaled, touched or ingested. The resin contains an acrylate (hydroxyethylmethacrylate "HEMA") in amounts prohibited in children's products by the Federal Hazardous Substances Act. Already created jewelry should be inspected to confirm it is fully cured. If there is liquid or any liquid residue present, the jewelry should not be worn and should be stored away from children. Once cured, the resin no longer presents the hazard.
The recalled window shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window shades are in violation of the federal regulations for window coverings and present a substantial product hazard. The window shades also violate federal regulations for labeling of window coverings.
Nutritional Fundamentals for Health (dba NFH), of Canada
🏠 Consumer Products Class II - Moderate
The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.