All Recalls

Edermy is recalling PIE PAK trolley systems (models P2HC-A, P2HC-S, P2HC) due to a lack of required 510(k) clearance.

MG Foods is recalling 10 oz Spicy Breakfast Burritos due to potential contamination with small hard plastic fragments.

Sodexo Stars Saccharin (Pink) packets are recalled due to undeclared aspartame, which may pose a risk to individuals with PKU.

Medtronic is recalling Octopus Nuvo Tissue Stabilizer (TSMICS1) due to incorrect tubing assembly that may affect surgical tissue stabilization.

Laerdal is recalling Compact Suction Unit 4 RTCA models due to potential electromagnetic noise interference exceeding safety standards.

Baxter is recalling Spectrum IQ Infusion Pumps (Model 3570009) because they were released without full occlusion alarm testing.

McCain Foods is recalling Sonic Tots frozen potato products due to potential contamination with small hard plastic fragments.

Teva is recalling Isotretinoin 40 mg capsules due to superpotency and subpotency concerns that may affect treatment efficacy or safety.

Waldemar Link is recalling the Endo-Model Replacement Plateau due to a risk of fracture that may cause the bushing to detach.

ADM Animal Nutrition recalls MasterPlex 75P 30/30 RU 55010CDH medicated cattle feed due to incorrect labeling causing monensin/urea toxicity.

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 Screw 16mm (Model A-5750.16/1) due to a packaging 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.

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.

Outside The Breadbox is recalling 8 oz Bread Crumbs due to undeclared egg and milk allergens.

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 seal defects that may cause fluid leakage, therapy delays, or contamination risks.

Olympus is recalling ShockPulse-SE Lithotripsy System generators due to a mis-wired component that may cause 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 due to a manufacturing defect that may cause the device to deform and lose function.

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

Philips is recalling Brilliance iCT CT systems because loose gantry rotor fasteners could cause parts to become unsecured or expelled.

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

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

Karison is recalling Panjiri due to an undeclared milk allergen.

Carrot Top Kitchens is recalling 8 oz Lime Ginger Hummus due to undeclared sesame.

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

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

HerbsForever is recalling Gastro Care herbal supplement capsules due to undeclared wheat.

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.