2,153 recalls tagged with “stop use immediately”.
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.
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.
Walmart recalls Ozark Trail 64 oz stainless steel insulated water bottles sold at Walmart due to a lid ejection hazard. The one-piece screwcap lid can forcefully eject when opened after liquids are stored inside, creating a risk of impact and laceration. Stop using the recalled bottles and contact Walmart for a full refund.
Dearlomum retractable mesh safety gates sold on Amazon by Signbaby are recalled. The gates violate federal expansion gate standards because a child's torso can fit through the base opening, creating a risk of serious injury or death from entrapment. Stop using the recalled gates immediately and contact Signbaby for a full refund; disassemble, destroy the mesh, and email a photo to regcards.team@gm
Creekliybear recalled its Pack and Play aftermarket mattresses sold on Amazon by Kbabyea on July 10, 2025. The mattresses exceed thickness standards and may not fit certain play yards, creating a suffocation entrapment risk. Parents should stop using the mattresses immediately and contact Kbabyea 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.
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.
SPPTTY recalled kids bicycles sold at Walmart after lead levels exceeded the federal lead content ban in multiple components and on the black paint used on pumps. The recall urges consumers to stop using the bicycles immediately. To receive a refund, dismantle the bicycles, photograph the setup, and email the photo to lishkjie@163.com; after destruction is verified, dispose of the bike.
Haoyunm braided crib bumpers sold on Amazon are recalled for a suffocation risk. The bumpers violate the Federal Safe Sleep for Babies Act. Stop using them immediately and contact Haoyunm for a full refund.
BioFire Defense recalled 130 FilmArray NGDS Warrior Panel NGDS-ASY-0007 kits distributed nationwide in the United States. The recall cites an increased risk of internal control failures when testing positive blood cultures. Clinicians should stop using the device immediately and follow recall instructions provided by BioFire Defense. Notification is by letter to affected facilities.
WLIVE recalled its Fabric 15-Drawer Dressers sold on Amazon after reports of tip-over and entrapment hazards. The dressers can tip when not anchored to a wall, posing serious injury or death risk to children and violating the STURDY standard. Consumers should stop using unanchored dressers and contact WLIVE for a full refund.
Boothwyn Pharmacy recalls 642 vials of semaglutide 2.5 mg/mL injection sold nationwide in the U.S. The recall cites subpotent drug with Class II designation. Consumers and healthcare providers should stop using the product immediately and contact Boothwyn Pharmacy for guidance.
Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.
Boston Scientific Neuromodulation recalls 25,260 Vercise DBS devices worldwide over wire breaks in rechargeable implantable pulse generators. The defect can prevent stimulation and trigger device removal. Patients should contact their provider for guidance and stop using affected devices immediately.
CURAD Alcohol Prep Pads recalled nationwide after tests found isopropyl alcohol levels subpotent. Medline Industries is the maker listed on recall documents. The issue concerns diluted potency below labeled concentration. Stop using immediately and contact Medline for guidance.
Walmart’s ReliOn sterile alcohol swabs are recalled nationwide due to subpotent isopropyl alcohol. The FDA notice lists 3,456,000 pads affected across 4,800 per case and 24 boxes per case. Consumers should stop use and contact Medline Industries or a healthcare provider for guidance.
Medline Industries recalled 6,669,874 units of Alcohol Prep Pads nationwide after detecting subpotent isopropyl alcohol. The pads were distributed nationwide. The recall is classified as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and contact Medline for guidance.
Rite Aid alcohol prep pads distributed nationwide are recalled after subpotent isopropyl alcohol levels were found below label concentration. Medline Industries, LP notified distributors and healthcare providers in a Class II recall dated July 7, 2025. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare provider.
Good Neighbor Pharmacy recalled 66,000 alcohol prep pads for subpotent isopropyl alcohol levels. The pads do not meet the labeled concentration, posing a risk to users. Consumers should stop using the pads immediately and consult their healthcare provider for guidance.