
FDA•MODERATE
Wellsley Farms Farm-Raised Atlantic Salmon
Wellsley Farms Farm-Raised Atlantic Salmon (32 oz) recalled for Listeria monocytogenes contamination.

Wellsley Farms Farm-Raised Atlantic Salmon (32 oz) recalled for Listeria monocytogenes contamination.

Italianway Import is recalling Vergani 1944 Milano Pandoro Classico Gluten Free due to potential Teflon fragment contamination.

LEO Pharma is recalling Adbry injection autoinjectors (NDC 50222-350-91, 50222-350-02) due to wool fiber contamination affecting sterility.

Ortho Dev. Trimax Pegged Drill Plates for the Lantern Knee System are recalled due to a manufacturing error causing excessive bone cuts.
2 products
LeMaitre Vascular is recalling Artegraft Vascular Grafts due to a labeling mix-up that resulted in incorrect lot information on packaging.

Medline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.

Boston Scientific is recalling EndoVive Safety PEG Kits due to potentially compromised sterile packaging on included ChloraPrep swabsticks.

Vee Tyre Taiga AT tires (LT235/85R16) may separate, causing tire failure and crash risk.

Volvo Trucks is recalling 2024–2027 VNL (4) vehicles for inadequate parking brake force in weight bias mode, risking rollaway.

Nova Bus is recalling 2013–2020 LFS transit buses; seat mounting rails may crack and cause seats to fall.

Vizzoni Dreamliner A/T tires (LT265/75R16) recalled for sidewall separation risk.

H & N Group is recalling 1 lb bags of frozen cooked medium shrimp due to potential Cesium-137 contamination.

Hortex Spring vegetable mix is being recalled due to potential contamination with glass.

Meitheal Pharmaceuticals recalls Cetrorelix Acetate injection kits (NDC 71288-558-90) due to missing or duplicated needles.

RefleXion X1 Radiotherapy System Model RXM1000 recalled for software defect causing incorrect radiation dose delivery.

Abbott is recalling ID NOW Influenza A & B 2 test kits (Model 427-000) due to an increased rate of invalid test results.

Harley-Davidson is recalling 2021–2026 Sportster S motorcycles due to upper triple clamp fracture risk.

SmartPak Equine is recalling smart & simple Turmeric Pellets due to elevated aflatoxin levels.

Oshkosh is recalling 2025–2026 NGDV vehicles; brake pedal mounting pin and retaining clip may be missing, risking brake failure.

Valley Springs is recalling 100% Natural Bottled Water (1 Gal) due to insanitary bottling conditions.
4 products
International Life Sciences is recalling the Artelon FlexBand Dynamic Matrix due to failure to meet bacterial endotoxin testing requirements.
3 products
BD Kiestra ReadA modules may experience connectivity issues after a reboot, potentially delaying plate retrieval.

Hitachi is recalling its Proton Beam Therapy System due to a software error that may cause inaccurate patient positioning during treatment.
2 products
Mercedes-Benz Metris (2020, 2022–2023) air bag control units may fail to deploy due to water accumulation.

Hyundai is recalling 2025–2026 IONIQ 5 and 2026 IONIQ 9 vehicles over high voltage battery short-circuit fire risk.

Hyundai is recalling 2026 Kona vehicles with defective front steering knuckles that may crack, causing loss of steering control.

Volvo is recalling 2017 S60L vehicles with defective door latches that may open unexpectedly.

Altec is recalling 2021–2025 Digger Derrick and AM Series Aerial Device vehicles; engine may start unexpectedly due to missing diode in power distribution module.

Toyo is recalling Open Country A/T III tires (265/70R18, 265/60R20) due to tread separation risk.

Tippy Toes Apple Pear Banana baby food is recalled due to potential patulin contamination.

Fagron Sterile Services is recalling Thiamine HCl 500 mg injection due to a lack of assurance of sterility.
5 products
Remel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.

Jaguar is recalling 2020–2021 I-PACE vehicles; high voltage battery may overheat and catch fire.

Diagnostica Stago is recalling the STA Liatest D-Di kit due to a positive bias that may cause inaccurate D-Dimer test results.
2 products
Somerset Therapeutics is recalling Dexamethasone Sodium Phosphate Injection (NDC 70069-025-10/01) due to out-of-specification impurities at expiry.

Diagnostica Stago is recalling STA Liatest Free Protein S kits due to the risk of inaccurate test results for normal patient plasma levels.

Fontaine Modification is recalling 2024–2025 Freightliner Business Class M2 vehicles over insufficient steering gearbox oil that may cause steering difficulty.

Daimler Coaches is recalling 2026 Mercedes Benz Tourrider transit buses with defective door control valves that may prevent door opening.

Ember is recalling 2026 E-Series and Overland Series travel trailers with incorrect cargo capacity labels that may cause overloading.

BMW is recalling 2026 228i and M235i Gran Coupe vehicles with rear lights that may not function properly, increasing crash risk.

React Health PHOENIX 5L Oxygen Concentrator recalled due to devices not meeting quality specifications.

Fresenius Kabi is recalling the Ivenix Infusion System LVP due to a risk of the cassette loading lever breaking during use.

Pure Solutions recalling 1 fl oz sleep formula bottles due to undeclared milk allergen from bovine colostrum.

Coco's Italian Market is recalling Cannoli Making Kits due to undeclared wheat and milk allergens.
2 products
Exactech is recalling the Equinoxe Ergo Modular Impactor Handle due to a missing cross-pin that may cause device failure.
2 products
GE Medical Systems is recalling Imactis CT-Navigation System (Models E85101LA, E85101LP) due to potential needle trajectory/tip position discordance.

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

Ford is recalling 2026 E-Transit vehicles over missing washers in the high-voltage battery pack that may cause electrical arcing and fire.

Ford is recalling 2023–2024 Transit vehicles over improperly secured engine crossmember that may cause loss of drive power or brake failure.

Pro Numb is recalling 5% Lidocaine Tattoo Numbing Spray due to cGMP manufacturing deviations.
2 products