All Recalls

Omnicell is recalling i.v.STATION syringe label stock due to the potential for mislabeled IV medication syringes.

GE Healthcare is recalling Omnipaque (iohexol) injection due to the presence of particulate matter.

Nova Bus is recalling LFS and LFS Artic transit buses (2016–2023) due to driver seat belt tension-relieving device failure.

Toyota and Lexus are recalling 2024–2026 Tundra, Tacoma, RAV4, and other models with incorrect load capacity labels that may cause overloading and crash risk.

Toyota is recalling 2022–2024 Lexus LX vehicles over front passenger air bag deployment risk from seat-frame clearance issues.

Storyteller is recalling 2024–2026 GXV Hilt RVs; entry steps may deploy while in transit, increasing crash risk.

Bentley is recalling 2025 Bentayga vehicles with incorrect tire placard information that may lead to wrong tire size or pressure.

Major Pharmaceuticals is recalling Memantine Hydrochloride Extended-Release 7 mg capsules (NDC 0904-6734-61) due to failed dissolution specifications.

Salute Seasonings Ground All Spice (16 oz) recalled for possible Salmonella contamination.

Ayco Farms is recalling whole fresh cantaloupes due to potential Salmonella contamination.

Foundation Medicine recalls PCT software v1.3.0 for Hamilton AutoLys STAR due to risk of spontaneous software closures during protocol execution.

Remel is recalling Yeastone Broth due to the potential for inaccurate antimicrobial susceptibility testing results.

Medline is recalling custom Namic Angiographic Manifolds due to the presence of particulate matter within the fluid path.

ICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.

White Oak Pastures Grassfed Ground Beef (16 oz) may contain metal; do not consume.

Winnebago is recalling 2017–2022 Brave, Itasca Sunova, Adventurer, and Sunstar motorhomes over undersized front turn signal lenses.

Daimler Coaches is recalling 2009–2020 Setra S417 and 2012–2019 S407 buses due to dashboard switch illumination failures that may distract drivers.

Hino is recalling 2026 NV7G, NV7D, NJ7E, NJ7D, NH7K, NE7D, and NH7G vehicles over incorrect U-bolt maintenance instructions that may cause bolt breakage and crash risk.

Booey's Dragon's Breath sauce is recalled for undeclared fish (anchovy) and sesame allergens.

Gentuity is correcting the HF-OCT Imaging System (Model G10-01) to address a software issue that may cause inaccurate length measurements.

Olympus is recalling Thunderbeat II Shears (Model TB2-0520FC) due to the risk of a distal tip component detaching during use.

Hologic is correcting Genius Review Station displays due to unauthorized configuration changes that deviate from validated settings.

Advanced Bionics is recalling M Zn-Air Battery Paks for cochlear implants due to a non-compliant battery door design.

Tangent Endoscopy is recalling single-use digital catheters due to a risk of fractures at the distal shaft tip.

Fagron is recalling Vancomycin HCl 1.5g/250mL injection due to sterility concerns and a potential detachment of the administration port part.

Mercedes-Benz is recalling 2026 GLC models with center rear seat belts that may fail to properly restrain child seats.

Hyundai is recalling 2026 Palisade and Palisade Hybrid (Limited/Calligraphy trims) over faulty third-row seat belt status indicator that may fail to alert unfastened occupants.

Altec is recalling 2025 AC Series Crane and DT Series Digger Derrick vehicles due to missing chassis lighting harness that may disable body or trailer lights.

Grand Design is recalling 2025–2026 Lineage motorhomes; entry steps may deploy while in transit, increasing crash risk.

Braun is recalling 2023–2024 Ram ProMaster vehicles with incorrect emergency exit window glass that fails FMVSS 226 safety standards.

Kia is recalling 2027 Telluride Hybrid second-row power seats that may fail to detect and stop for a person.

Exchange Select Honey Lemon Cough Drops are recalled due to manufacturing facility inspection observations that may impact product quality.

Leading Pharma is recalling Furosemide Tablets 80 mg (NDC 69315-118-01) due to N-nitroso-Furosemide above recommended limits.

Foundation Medicine is recalling Sequencing Agent SEQ0067 component of FoundationOne CDx due to possible false-positive BARD1 variants.

Centinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up between 5mm and 6mm sizes.

Riverence is recalling Smoked Trout Dip due to an undeclared milk allergen.

Amneal is recalling tramadol 50 mg tablets (NDC 60219-2348-5) due to elevated N-nitroso-desmethyl-tramadol impurity.

Teva Pharmaceuticals is recalling Clonidine Transdermal System 0.2 mg/day due to the use of an unapproved raw material during manufacturing.

International is recalling 2023–2027 IC Bus CESB and 2025–2027 EVSB school buses over insufficient epoxy on body panel joints that may separate in a crash.

Terex is recalling 2019–2026 General 65, 80, 95, C4000, C5000, C6000 digger trucks; pole guide arm may fall due to cracked weld.

Lippert is recalling certain 8K axles with incorrect seals that can cause oil leakage, bearing failure, and wheel loss.

GM is recalling 2018–2019 Silverado and Sierra Crew Cab trucks over roof rail air bag inflator end cap detachment or rupture risk.

Ford is recalling certain 2022–2025 Lincoln Navigator, Nautilus, Aviator, and Explorer vehicles over Image Processing Module resets causing loss of rearview camera and ADAS features.

Boston Scientific is updating software for Essentio, Proponent, Accolade, and Altrua 2 pacemakers to address dual-chamber device performance.

Integra LifeSciences is recalling Cytal Wound Matrix 2-Layer 5x5 cm dressings due to out-of-specification endotoxin results.

Philips is recalling AneurysmFlow software due to unreliable MAFA ratio data that may lead to incorrect clinical decisions.

B. Braun is recalling Streamline Bloodline Sets for Dialog iQ machines due to a risk of air bubble accumulation in the arterial line.

Elekta is recalling the Leksell Vantage Arc System due to a defect in the locking mechanism that may cause coordinate shifting during procedures.

Medline is recalling various neuro sponges due to higher-than-expected endotoxin levels.

American Contract Systems is recalling Medline Namic Angiographic Control Syringe kits due to a risk of syringe disconnection during use.