
FDA•MODERATE
Hotline Fluid Warming Set
ICU Medical is recalling Hotline Fluid Warming Sets due to a risk of leakage at the tubing-to-connector bond.

ICU Medical is recalling Hotline Fluid Warming Sets due to a risk of leakage at the tubing-to-connector bond.

Paragon 28 is recalling the Phantom Hindfoot TTC/TC Ball Tipped Guide Rod (item P31-955-1800-S) due to sterile packaging breaches.

Altec is recalling 2024-2026 AT Series vehicles due to improperly heat-treated turntable fasteners that may fail and cause separation.

Boston Scientific recalls FARADRIVE Steerable Sheath Clear IDE over valve damage risk that may cause air embolism.
4 products
Foretravel recalls 2027 Realm Presidential Motorcoaches over MaxxAir fan PCB overheating fire risk.
2 products
Evenflo recalls Reo by Revolve360 child seats over headrest shift risk in a crash.

Great Dane recalls 2027 Champion dry van trailers missing rear impact guard extension channels, increasing crash injury risk.

Turtle Top recalls 2026 Terra Ford Transit buses: wheelchair lift contactor may fail, causing unintended movement and injury risk.

Currey & Company is recalling Nottaway chandeliers due to an electrocution hazard caused by a lack of proper electrical grounding.

Hollis 200LX diving regulators are recalled due to a risk of drowning from potential inlet tube breakage.

Jobon torch lighters are recalled for lacking child-resistant mechanisms, posing fire and burn hazards to users.

Liizousuda paint thinner is recalled because its non-child-resistant packaging poses a poisoning and chemical pneumonia risk to children.

Madewell is recalling women's sweaters due to a violation of federal clothing textile standards, posing a serious burn and injury risk.

Noerishia adult portable bed rails are recalled due to a serious entrapment and asphyxiation hazard.

Oitnlaughter LED finger lights are recalled due to a battery ingestion hazard that can cause serious injury or death.

Panasonic is recalling model NB-G200 electric toaster ovens due to shock and fire hazards from insufficient power cord insulation.

Boon PIVOT toddler tower step stools are being recalled due to tip-over and fall hazards that pose a risk of serious injury or death.

Wade Logan 9-drawer fabric dressers are recalled due to tip-over and entrapment hazards that violate federal safety standards.

Tosoh is recalling ST AIA-Pack Testosterone test kits due to potential for inaccurate results that may impact clinical treatment decisions.

International is recalling certain MV and HV vehicles because the battery cable may short circuit, posing a fire risk.

Altec is recalling 2013-2025 AP45A trucks due to a damaged boom stow switch wire that may overheat and cause a fire.

International is recalling 2025-2027 IC Bus EVSB and CESB school buses due to body panel joints that may separate during a crash.

Land Rover is recalling 2021-2025 Discovery Sport vehicles due to a rearview camera defect that may reduce driver visibility.

Chrysler is recalling 2026 Jeep Gladiator and Wrangler vehicles due to steel wheels that may crack or detach, increasing crash risk.
2 products
IC Bus CECB buses recalled: body panel joints may lack epoxy, risking separation in crashes.

CareFusion is recalling BD ChloraPrep Clear sterile solution applicators due to a potential lack of sterility from incomplete packaging seals.

Daavlin recalls Photera 400 phototherapy device due to incorrect UV sensor gain causing inaccurate output.
3 products
Medline recalls Total Knee Pack kits with Zimmer Biomet mixing bowls and spatulas over sterility risk.
2 products
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System is recalled due to an out-of-specification sterilization dose.

Medtronic recalls DLP Pediatric Arterial Cannula (CFN 77010) over loose foreign material with trace blood.
2 products
Papablic is recalling replacement brush heads over a choking hazard from breakage.
2 products
Orange EV is recalling certain e-TRIEVER, T-Series, and HUSK-e terminal trucks due to frame rails that may crack and separate.
E-One is recalling 2025-2026 Commercial, Typhoon N, and Cyclone N emergency vehicles due to a risk of sudden loss of drive power.

Nissan is recalling certain Armada, QX56, and QX80 vehicles with 22-inch wheels due to incorrect GAWR labels that may lead to overloading.

Chiesi USA is recalling Cleviprex (clevidipine injectable emulsion) 50 mg/100 mL vials due to a lack of assurance of sterility.

Bell Pharmaceuticals recalls carbamide peroxide 6.5% earwax removers (CVS Health, Clinere, TopCare, etc.) for subpotency.
11 products
Orthofix recalls MINIRAIL Standard Lengthener (M101) over incorrect labeling.
8 products
Winnebago is recalling 2027 Navion and View RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board fire risk.
2 products
Hyundai is recalling 2025 Kona Electric and 2026 Kona vehicles because the rear center seat belt buckle may fail to restrain occupants.

Ford is recalling 2016-2019 Explorer vehicles because roof rail covers may detach, creating a road hazard.

Ford is recalling 2020-2027 Aviator and 2020-2026 Explorer vehicles because a faulty seat switch may cause second-row seats to move unexpectedly.
Ford is recalling ITRM accessory kits for 2021-2026 F-150s due to a potential loss of trailer brakes and lighting.

Wabash is recalling 2025-2026 Dry Freight trucks because broken liftgate deck pins may cause the platform to fall, posing an injury risk.

Padagis is recalling 15 g tubes of Nystatin Cream USP due to subpotent drug results found during stability testing.

GE HealthCare recalls Optima XR200/220/240amx systems after column replacement due to risk of arm drop and patient injury.
3 products
Nutricia recalls Liquid Hope and Nourish organic meal replacement formulas due to subpotent Vitamin A.
2 products
Boston Scientific is recalling the Rapid Refill Continuous Injection System due to a risk of syringe disconnection during use.

ICU Medical recalls Plum Duo Infusion Pump v1.2.3 due to risk of delivering up to twice the programmed VTBI.
2 products
Argon recalls Transvenous Pacing Electrode Trays due to non-sterile lidocaine ampules in kits.
6 products
Abiomed recalls Impella RP Flex introducers over sheath leakage risk.
13 products