
FDA•MODERATE
SnapshotGLO Wound Imaging Device
Kent Imaging recalls SnapshotGLO wound imaging devices due to battery charging failure.

Kent Imaging recalls SnapshotGLO wound imaging devices due to battery charging failure.

Micro Therapeutics recalls Pipeline Flex Embolization Devices due to incorrect labeling of implant sizes.
4 products
AVID Medical recalls Halyard Standard Line Insertion Pack (Model PVHM234-01) over silicone seal defects causing leakage.
Emano Flow v2.0.0 recalled due to audio sampling mismatch causing biased flow rate and volume estimates.

Boston Scientific recalls TheraSphere 360 Y-90 Platform due to software anomaly causing incorrect dose calculations.

Olympus recalls UHI-4 insufflation unit over unexpected display shutdown and air delivery loss.

Coach and Equipment recalls Phoenix/Metrolite buses with S-Series wheelchair lifts due to contactor failure that may prevent stopping.

ATC recalls 2026 RM500 and RM700 trailers over winch remote incompatibility that may cause unexpected movement.
2 products
Heil recalls 2025-2026 side loader garbage trucks with HH Technologies ReVamp high voltage cabinets (part 372-9585) over water intrusion risk.
2 products
Volkswagen recalls 2024-2026 Atlas vehicles over rearview camera display failure.

Daimler Trucks recalls 2026-2027 Freightliner models over low beam headlight software error that reduces visibility.

Hiab recalls K-HiPro 425 and 505 cranes due to weld fatigue that may cause column collapse.

PT Organics recalls Peter Rabbit Organics Banana & Strawberry puree pouches due to possible plastic strands.
2 products
Medtronic is recalling the Ventriculostomy Kit due to endotoxin levels that exceed safety limits for cerebrospinal fluid contact.

Penumbra is recalling the RED 68 Reperfusion Catheter due to a manufacturing issue that may cause the device to fracture during use.

Wilcox is recalling all BOSS Xe aiming lasers to implement a safety-related software enhancement.
3mensio software may report inaccurate cardiovascular measurements when analyzing specific Philips 3D echo datasets.

The Silent Nite Sleep Appliance (Model SILNT) is being recalled because it lacks required FDA clearance.

Ember recalls 2027 Overland, E-Series, and Touring trailers over incorrect VIN on certification label.

Ford recalls 2026-2027 Explorer and Aviator over driver's seat that may recline unexpectedly.

Olympus is recalling the 4K UHD LCD Monitor (model OEV321UH) due to a potential connector fault that may cause image loss or abnormalities.

AVID Medical is recalling the Eye Pack convenience kit (Model LVEY27) due to an incorrect concentration of Betadine solution.

SeaSpine is recalling the Polyaxial Head due to a manufacturing error that may cause the component to detach during surgery.

Ford recalls 2021-2026 Bronco and Bronco Raptor over wiring harness short circuit fire risk.

Blue Bird recalls 2022-2027 Vision buses over brake line damage that may cause fluid leak, fire, or crash risk.

Blue Bird recalls 2022-2027 Vision school buses over brake line damage risk from cotter pin contact.

Cat & Jack children's sandals are recalled due to a choking hazard from detachable pearls on the footwear.

Rising Pharma recalls Cyproheptadine HCl Syrup 2mg/5 mL due to crystallization and floating particles.

Major Pharmaceuticals recalls Levothyroxine 25 mcg tablets due to subpotency.
12 products
Ascend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets (10 mg/20 mg) due to failed dissolution specifications.

Bionpharma recalls Divalproex Sodium 500 mg tablets due to foreign tablets/capsules.

Ferno is recalling the Power F2 Powered Fastening System due to a risk of the rail mechanism lodging and preventing stretcher movement.

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.
