Vitaquest is recalling 11 brands of iron supplements (Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean, Sakara) with non-child-resistant packaging.
ShymeryDirect LED lights with accessible CR2032 coin batteries pose ingestion hazard to children; can cause serious injury or death.
Wybotics is recalling Osprey 700 Max and S1 robotic pool vacuums over lithium-ion battery overheating risk.
Yeeluzan pool drain covers violate federal entrapment safety standards, posing drowning risk.
Silks is recalling children's loungewear sets (sizes 2T–13/14) sold online January 2024–September 2025 due to flammability standard violations and burn hazard risk.
Snooz is recalling Breez 2-in-1 Smart fans (BZ10, BZ02 serial numbers) due to power connector corrosion that can cause overheating and fire risk.
Major Pharmaceuticals is recalling Omega-3-Acid Ethyl Esters Capsules 1 gram (NDC 0904-7495-06) due to failed capsule shell specifications.
Stryker is recalling the FluidSmart Urology Tube Set due to the distribution of nonconforming products.
Apotex is recalling Desmopressin Nasal Spray (NDC 60505-0815-0) due to defective bottle caps with missing or dislodged liners.
3 products
Pure Ground Ingredients is recalling Organic Peppermint Leaf Powder due to potential Salmonella contamination.
Hologic is recalling 15+ models of Selenia Dimensions Mammography Systems due to potential internal bolt failure.
2 productsMedtronic is recalling the A810 software app for SynchroMed pumps due to a display error that can disrupt the programmed infusion schedule.
2 products
Becton, Dickinson and Company is recalling 15+ models of Swan-Ganz Catheters due to a risk of hub leakage or breakage.
3 products
Marquez Brothers International is recalling Bulk Horchata Powder due to undeclared milk, which poses a risk to those with milk allergies.
3 products
Hikma is recalling Alendronate Sodium Oral Solution 70 mg/75 mL (NDC 0054-0282-59) due to out-of-specification assay results.
Becton Dickinson is recalling BD GasPak EZ CO2 and Campy Gas Generating Pouch Systems due to insufficient carbon dioxide production.
2 products
CVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
Teva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products
Kirkland Signature Traditional Madeleines are recalled due to undeclared hazelnut and soy lecithin.
Fresenius Medical Care is recalling Delflex Peritoneal Dialysis Solution due to potential bag leaks and a lack of sterility assurance.
2 products
Quidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
MicroVention recalls LVIS Intraluminal Support Devices (REF 214022-CAS, 214518-CAS, 213517-CAS) due to dimensional nonconformance risking vessel injury or thrombosis.
Liquid Blenz Soursop Bitters are recalled due to potential Clostridium botulinum contamination and unauthorized health claims.
13 products
Dakota Honey Company is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products
DePuy Synthes is recalling the Attune Revision Hinge Femoral component due to a potential loss of sterility from packaging defects.
9 products
Walker Honey Co. is recalling Fain's Blackberry Honey Spread due to potential stainless steel or plastic particle contamination.
10 products
Lundberg Family Farms is recalling 32 oz Jasmine White Rice due to potential foreign material contamination.
Grace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
Coluans Christmas Light-Up Rings (model SJP-50) recalled for accessible button cell batteries posing serious ingestion hazard to children.
Beestech spiral tower toy (model Bee-210316-01) recalled for choking hazard; violates small ball ban for children under 3.
E Mishan recalls Granitestone Diamond Pro Blue sauté pan sets (UPC 0-80313-08131-6) due to detachable metal cap that can eject when heated, causing impact and burn hazards.
TecFlox is recalling Minoxidil Topical Solution bottles lacking child-resistant packaging, posing poisoning risk to children.
HTRC and Haisito T400 battery chargers can ignite, posing a fire hazard and risk of serious injury or death.
ELENKER portable bed rails (models HFK-5115, HFK-5116, HFK-5124) recalled for entrapment and asphyxiation risk; lack required safety labels.
Ocun is recalling Condor HMS Triple Carabiners (batches 24003xx–25006xx) due to gate malfunction risk causing falls.
Samson International recalls Universal Broadmoor canopy bed frames (models M24109230, M24109240, M24107230, M24107240) due to collapsing canopy beams.
Sam's Club recalls Member's Mark children's pajama sets (sizes XS–XL) for violating flammability standards and posing burn hazard.
Tuymec Minoxidil Hair Growth spray bottles lack required child-resistant packaging, posing poisoning risk to children.
Gavoyeat Halloween Light-Up Rings recalled for accessible button cell batteries posing serious ingestion hazard to children.
Sangohe bed rails models 504E and 504Q recalled for entrapment and asphyxiation risk; sold on Amazon August 2023–February 2026.
ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich is recalled due to undeclared sesame.
B. Braun is recalling 3000 mL Sterile Water for Injection USP bags distributed nationwide due to potential sterility and leakage issues.
4 products
Huvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
Huons is recalling Lidocaine HCl injection 1% 5 mL vials due to a lack of assurance of sterility.
9 products
Hemu Trading is recalling 150g packages of Enoki Mushrooms due to potential Listeria monocytogenes contamination.
Siemens is recalling epoc BGEM BUN Test Cards due to the risk of inaccurate pH and carbon dioxide results that may lead to improper treatment.
Merit Medical Systems is recalling the Philips Bridge Prep Kit due to potential catheter resistance during use.
4 products
Cook is recalling Centimeter Sizing Catheters due to a risk of marker band breakage, which may cause vessel injury or life-threatening harm.
3 products
Intuitive Surgical is recalling USM arm sub-assemblies for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products
DFI is recalling the One Step 10A in vitro diagnostic test because it was distributed without required FDA premarket clearance or approval.
7 products