All Recalls

Terex is recalling 2025 TL-Series, LT-Series, LTM40, HR40, HR46, and SCM55 areal devices with overheating hydraulic control valves.

Rising Pharmaceuticals is recalling Furosemide Tablets 40 mg (NDC 64980-563-10) due to foreign substance contamination.

Diva Fam is recalling Sea Moss Gel Superfood due to potential Clostridium botulinum contamination.

Medartis is recalling APTUS 2.5 TriLock screws (Model A-5750.16/1) due to a potential mix-up with 2.8mm screws.

Maquet is recalling Venous Bubble Sensors for 3/8" x 3/32" tubing due to cable durability issues that may cause sensor failure.

Land Rover is recalling 2026 Range Rover Sport vehicles with incorrect weight information on the certification label, increasing crash risk.

Goodyear is recalling Cooper Discoverer SRX 255/50R20 tires with incorrect Tire Identification Numbers.

FDR Visionary Suite X-ray generators are being recalled due to a risk of overheating and smoke caused by faulty electromagnetic contactors.

Diowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.

Island Crab Corporation is recalling Smoked Grouper Dip due to undeclared milk, eggs, and sodium metabisulfite.

Medline is recalling kits with Tego Connectors due to defective silicone seals that may cause leakage or therapy interruption.

Olympus is recalling ShockPulse-SE lithotripsy generators due to a mis-wired component that may cause system reliability issues and treatment delays.

Isla Rae magnetic wireless chargers (model RM5PBM) sold at T.J. Maxx and Marshalls can explode, posing fire and burn hazards.

BabyBond retractable safety gates (model SH20.006DB) recalled due to entrapment risk between gate and floor.

Agrish adult portable bed rails (models 2512, 2513, 2516) pose entrapment and asphyxiation risk; violate mandatory safety standard.

DR Power Equipment is recalling walk-behind and tow-behind leaf vacuums (models WL33006DMN, LL21009DMN, LLVX13, and others) due to laceration hazard from loose pieces or debris ejection.

Joyful Journeys baby loungers recalled for fall and entrapment hazards due to low sides and wide foot openings; sold online Dec 2023–Oct 2025.

Kori Gey Water Elf Kit recalled due to easily accessible button cell battery posing ingestion hazard to children.

Lterfear Multifunction Pounding Game (model D888) recalled for detachable high-powered magnets posing serious ingestion hazard to children.

Julie and Judah pajama pants and shorts violate children's sleepwear flammability standards, posing a burn injury risk.

Vasicar 18-Drawer Dressers (models VR-US18D) sold on Amazon pose tip-over and entrapment risks to children if not wall-anchored.

RH is recalling 48" and 60" Natural Antler Chandeliers (SKUs 10036671, 10035099) that may detach and fall when hung at angles on vaulted ceilings or sloped beams.

YOLAAH Bed Rails model BR-01 pose entrapment and asphyxiation hazards and lack required warning labels.

NFSVLB Baby Bath Seat Model ZY2025 recalled for tipping and entrapment risk; poses drowning hazard.

PNW Components is recalling Loam Pedal Gen 2 mountain bike pedals due to axle cracking that can cause detachment and falls.

Kalencom is recalling SARO Braided Crib Bumpers (Model 1374) due to suffocation risk; violates federal crib bumper ban.

Rattan 6-Drawer Dresser model YD001 poses tip-over and entrapment hazard to children; must be wall-anchored per STURDY Act.

Sangohe adult portable bed rails (Model KDB504A01FT) recalled for entrapment and asphyxiation risk; lack required safety labels.

Rich Products Corp is recalling Gluten Free 14" Seasoned Vegan Pizza Crust due to undeclared milk and egg allergens.

Hannaford hamburger dill pickle chips (UPC 0 41268 14889 9) recalled due to glass contamination.

Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Model KD-V411M-1520) due to a risk of device deformation and performance loss.

Medline is recalling various surgical and biopsy convenience kits due to potential issues with sterilization and packaging equipment calibration.

Philips is recalling Brilliance iCT and Spectral CT 7500 gantry rotors due to a risk of unsecured parts becoming displaced during rotation.

Wanli is recalling Aptany Eco Sendero M/T2 tires (LT265/75R16) due to sidewall separation risk.

Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient record linking.

Medline is recalling convenience kits due to potential sterilization issues that may affect product sterility.

Karison is recalling Panjiri due to an undeclared milk allergen.

Vantive is recalling the Prismaflex M100 Set due to a potential deaeration chamber dislodgement from the control unit.

Straumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.

Blue Bird is recalling 2026 Vision and All American buses with QRT-Deluxe and QRT-Max wheelchair restraints that may not lock.

Encon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.

BioMérieux is recalling 30+ VITEK 2 susceptibility card variants over risks of quality control failures and false resistant test results.

Raz Design is recalling various mobile shower commode chairs due to a seat bracket installation issue that may cause seat instability.

Medline is recalling the Nail Kit (model DYKM1528) due to potential sterility issues with the included saline wound wash.

Encore Medical is recalling EMPOWR acetabular liners and knee inserts due to a packaging discrepancy that may cause surgical delays.

LS2 Rebellion helmets (XL, XXL, July 2024–July 2025) recalled for inadequate impact protection.

Rivian is recalling 2022–2025 R1S and R1T vehicles; toe link joint may separate after service, increasing crash risk.

Blue Bird is recalling 2022–2024 All American transit buses over a loose 12-volt cable that may cause loss of brake assist, drive power, and steering.

Halyard Transport Bag Kit LIFE0080-01 recalled due to Tyvek bag seal issue that may compromise sterility.

Alphatec Spine is recalling the ATEC Lateral Navigation Disc Prep Osteotome due to a design defect in the navigated array connection.