Browse through 3,495 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
DJO Surgical is recalling 447 ALTIVATE Reverse Glenoid Reamer Sleeve devices distributed nationwide in the United States. The device may kick or bind up during or immediately prior to use. Healthcare providers and patients should stop using the device and follow recall instructions issued by Encore Medical, LP via email.
DJO Surgical recalled 907 units of the ALTIVATE reverse wedge glenoid reamer boss drill 6.5mm sold nationwide in the United States. The device may kick or bind up during use. Healthcare providers and patients should stop using the device immediately and follow recall instructions from Encore Medical, LP.
DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.
DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The products are contaminated with the bacteria Burkholderia cepacia, which poses significant health risks. Consumers must stop using the soap immediately and contact DermaRite for guidance.
DermaRite Industries’ DermaKleen antiseptic lotion soap is recalled nationwide after contamination with Burkholderia cepacia. The Class I recall covers 11,321 bag-in-box units sold nationwide. Consumers are urged to stop using the products and contact the company for guidance.
Deale International is recalling CasaClean Handheld Steamers DF-958 sold on HSN for burn risk. The steamers can leak steam or spray boiling water, creating a serious burn hazard. Consumers should stop using the product and contact Deale for a full refund.
Babyletto recalled its Kiwi Electronic Recliner and Glider chairs due to an overheating USB module. The USB module can overheat and spark, posing an overheating hazard. Consumers should stop using the recalled chairs and contact Babyletto for a free repair kit.
4,300 SureStep Foley Tray System Bardex I.C. Complete Care catheter tray units are recalled nationwide by C.R. Bard. The trays may contain incorrect inserts, creating a risk of infection or an allergic reaction. Healthcare providers and patients should stop using the device and follow Bard’s recall instructions.
Primark recalled the DTR Stitch Scented Highlighters 4-pack sold by Primark due to phthalate exposure risk. The highlighters resemble slushies with straws and carry the Kimball Number 0688701. Consumers should stop using them and return to Primark for a full refund.
Five thousand seven hundred three bottles recalled nationwide for microbial contamination with Burkholderia cepacia. DermaRite Industries LLC issued the recall on July 17, 2025. The product is PeriGiene Health Care Antiseptic, 222 mL bottles. Consumers should stop use and contact DermaRite for guidance.
CR Bard recalled 3,670 SureStep Foley Tray System A942216 Foley Catheter Trays nationwide after discovering incorrect inserts. Mislabeling could cause infection or allergic reactions. Healthcare providers should stop using the device immediately and follow recall instructions from the manufacturer.
iStore recalled its Magnetic Wireless Power Bank, 5000 mAh, imported by Tomauri. The lithium-ion battery can overheat and ignite while charging. Only IST-09991/W05 units are affected; consumers should stop using the recalled power bank and return it for a full refund.
Tractor Supply recalled three Traveller aluminum loading ramps on July 17, 2025 after determining a fall hazard. The ramps can bend or break under load. Stop using the recalled ramps and seek a full refund from Tractor Supply.
VIVI recalled 36-volt lithium-ion batteries included with certain VIVI brand e-bikes sold by VIVI. The batteries can overheat and pose fire and burn hazards. Stop using affected e-bikes immediately and contact VIVI for a free replacement battery and charger.
DermaRite Industries recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025 due to microbial contamination. The product, sold nationwide, carries NDC 61924-189-08 and Lot 40187.2 with an expiration date of February 2026. Consumers should stop using the product immediately and contact DermaRite for guidance.
C.R. Bard Inc. recalls 4,300 SureStep Foley Tray System Lubri-Sil I.C. Complete Care infection control Foley catheter trays nationwide in the United States. The trays may contain incorrect inserts that misrepresent material composition. The mismatch could trigger infections or allergic reactions. Health care providers should stop use and follow recall instructions immediately.
Quest International recalls 376 Measles IgM ELISA kits nationwide in Utah, Texas and Arizona after discovering the product lacks premarket approval or clearance. The high-risk health device carries a Class II designation. Stop using the device immediately and follow manufacturer recall instructions.
Stryker Communications recalls 40 surgical light systems nationwide after reports of stress lines in the powder coating. The devices include CH00000001 and the SLX to Oculan NFC Upgrade Kit, P60034. The recall is active as of July 15, 2025. Patients and healthcare providers should stop using the devices immediately and follow manufacturer recall instructions.
AUGNORYE recalled padded cushioned crib bumpers sold on Amazon by YIXIA. The bumpers can obstruct an infant's breathing, creating a suffocation hazard. Parents should stop using immediately and contact YIXIA for a full refund.
Giant Bicycle recalls Momentum Vida E+ electric bicycles after a fork crash hazard. The recall affects bikes with specific serial numbers. Stop riding and contact Giant Bicycle for a fork replacement.