
FDA•MODERATE
Medline Medcrest Surgical Gowns
Medline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
Medline is recalling Medcrest surgical gowns due to fabric delamination risks that may lead to infection or delays in patient care.
3 products
Lutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.

Honda is recalling 2023–2025 CMX300, CMX500, and CL500 motorcycles; handlebar lock screw may detach and interfere with steering.

Rolls-Royce is recalling 2020–2026 Cullinan vehicles; loose bolts may damage rear seat belt webbing and reduce crash protection.

Vision Wheel is recalling aftermarket aluminum wheels (part numbers 640-6744GBMF38, 640-6765GBMF40, 640-7710GBMF40, 640-7744GBMF40, 640-7765GBMF40) that may crack and cause loss of vehicle control.
2 products
Gillig is recalling 2021–2026 Low Floor transit buses over air compressor intake pipe contacting fuel line, risking fuel leak and fire.

Chrysler is recalling 2024–2026 Jeep Wagoneer S vehicles; liftgate hinge cover may detach and create a road hazard.

Gillig is recalling 2023–2026 Low Floor transit buses over high voltage cable overheat and fire risk.

Rising Pharmaceuticals is recalling Temozolomide Capsules 5mg (NDC 16571-816-51) due to failed impurities and degradation specifications.

Mylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.

Radnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.

Artelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.
3 products
Beckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.
2 productsHealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.
2 products
Boston Scientific is recalling EndoVive Safety PEG Kits due to compromised seals on the included antiseptic swabsticks.

ATC is recalling 2023–2026 PL700 and PL750 trailers over carbon monoxide entering the cabin from generator exhaust.

Mack is recalling 2022–2027 TerraPro trucks; ECU software may allow engine start in gear, risking unexpected movement.

Volkswagen is recalling 2025–2026 Jetta vehicles over loose transmission ground wire fire risk.

Volvo is recalling 2025–2026 EX30 and 2026 EX30CC vehicles over a faulty seat belt warning chime system.

ARBOC is recalling 2018–2026 Spirit of Freedom/Mobility buses over rear ABS malfunction that increases crash risk.

Endo-Model Replacement Plateau is recalled due to a risk of bushing detachment from the screw shaft caused by longitudinal fractures.
13 products
Instrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause ejection and delay patient results.
20 products
Physio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that could impact therapy delivery.
2 products
Medartis is recalling APTUS 2.5 TriLock Screws (model A-5750.16/1) due to a mix-up with 2.8mm screws.
2 products
Palmetto Gourmet Foods is recalling Vegetarian Chicken Flavor Ramen 3oz packages due to undeclared Yellow #5.
2 products
Exactech recalls Equinoxe Core Instrument Kit and Ergo Impactor Handle over missing cross-pin risk.
2 products
Raz Design is recalling various mobile shower commode chairs due to a seat bracket issue that may pose a fall risk to users.
2 products
BD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.

IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.

Mercedes-Benz is recalling 2026 GLA 250 vehicles over an incorrectly installed door cable that may prevent opening from inside.

Pebble is recalling 2026 Flow trailers; solar panels may detach due to adhesive failure.

Kia is recalling 2027 Telluride and 2026 K4 vehicles over rear seat belt buckles that may not latch properly.

Tomum Minoxidil Hair Growth Treatment is recalled because the non-child-resistant packaging poses a poisoning risk to young children.

Cubimana Island Storm building sets (Model HG1004) are recalled because the LED light's battery compartment poses a serious ingestion hazard.

Forever 21 Kids Disney Mickey Mouse Pajama Pants are recalled for violating federal flammability standards, posing a serious burn hazard.

Kirkman recalls Vasocaine Spray and Zone 1/2 Lidocaine Creams over unsupported expiry dates.
3 products
Forest River is recalling 2026 Impression fifth wheel trailers with improperly stripped wires that may cause electrical arcing and fire.

Escape Trailer recalls 2025 E17, E19, E21, E5.0 trailers; spare tire carrier may detach due to welding defect.

Forest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes over improper electrical distribution panel grounding that may cause electrocution risk.

Webasto is recalling CV Standard Gen1 Batteries (part nos. 5613175, 5610618, 5610610) over potential failure causing crash or fire risk.

GM recalls 2025–2026 Express and Savana Cutaway vehicles with damaged tire sidewalls that may cause sudden air loss.

GM recalls 2025–2026 Silverado 3500 and Sierra 3500 dual-tank models for fuel pump failure risk causing engine stall.

Mitsubishi Fuso is recalling 2024–2025 Rizon trucks (FEC7K, FEC9K, FECXK) for electrical control unit errors that may prevent driving.

Toyota is recalling 2021–2024 Highlander and Highlander Hybrid vehicles over second-row seat back latch failure.

Medline is recalling the Nail Kit (model DYKM1528) because the included sterile saline wound wash may not meet sterility requirements.
5 products
Kumho is recalling Solus TA11 tires (225/60R16) due to potential tread separation and crash risk.

Audi is recalling 2019 Q8, A7, A6 vehicles; lane departure warning may be deactivated due to software error.

Major Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.

Olympus is recalling the MAJ-210 single use biopsy valve due to the potential for rubber fragments to detach during use.
2 productsDatascope is updating the Instructions for Use for the CS300 IABP (software version C.01) to correct battery runtime and cycle specifications.
2 products