All Recalls

Prestige is recalling Supernova and Typhoon butane lighters because they lack required child-resistant mechanisms, posing fire and burn risks.

Happiness Light LED lights are recalled due to a serious battery ingestion hazard that can cause severe internal chemical burns and death.

Muscccm pool drain covers are recalled due to entrapment and drowning hazards for failing to meet federal safety standards.

Member's Mark 7' Pre-Lit Twinkling Buck is recalled due to a burn hazard caused by an overheating resistor.

Shenzhen Shijingjie is recalling male-to-male extension cords (models RY-US-06 and RY_US-1.5) due to electrocution, fire, and CO poisoning risks.

ShymeryDirect LED lights are recalled due to a serious battery ingestion hazard and missing safety warnings.

Yeeluzan pool drain covers are recalled due to entrapment and drowning hazards, as they violate federal safety standards.

Pure Palm Medjool Dates recalled due to mislabeling—coconut-covered bites labeled as regular date bites.

HydroPeptide Clear Alliance Serum recalled due to benzene contamination.

Cipla recalls Cinacalcet HCl 30 mg tablets over N-Nitroso impurity above acceptable limit.

Exchange Select Honey Lemon Cough Drops recalled over quality concerns from FDA inspection.

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

LinkBio CORE Workstation (87-9136) may display incorrect Planning Date on Start Case menu.

Philips is recalling AneurysmFlow software because the MAFA ratio provides unreliable prognostic data for aneurysm treatment decisions.

Arjo Tenor patient lifts (Models KHA1000 US, KHA1010 US) recalled for actuator failure risk causing sudden arm drop.

BISSELL is recalling Steam Shot handheld steam cleaners due to a burn hazard from attachments that can detach and expel hot water or steam.

Easymake adult portable bed rails are recalled due to an entrapment and asphyxiation hazard that violates federal safety standards.

SCUBAPRO is recalling Monorail Weight Pockets for BCDs because the D-ring handle can detach, posing a drowning hazard.

Maitys magnetic drinkware charms are recalled due to an ingestion hazard from loose magnets that can cause serious injury or death.

The products lack required child-resistant packaging, posing a risk of serious injury or death from poisoning if swallowed by young children.

Wybotics is recalling Osprey 700 Max and S1 robotic pool vacuums due to battery overheating, posing burn and fire hazards.

Silks children's loungewear sets are recalled for violating federal flammability standards, posing a serious burn risk to children.

SNOOZ is recalling Breez 2-in-1 Smart Bedroom fans due to an overheating fire hazard caused by power connector corrosion.

Cipla recalls Lanreotide Injection 120 mg/0.5 mL over sterility assurance concerns.

GE Healthcare recalls Omnipaque (iohexol) Injection 350 mg/mL due to particulate matter.

Stryker is recalling tourniquet cuffs that may detach from the bladder, preventing the device from maintaining pressure.

Blaine Labs recalls multiple topical antiseptic/antifungal gels and creams due to Lysinibacillus fusiformis contamination.

Divided Sunset Multi Collagen Peptides are recalled for failing to declare egg and fish allergens on the product label.

Viatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.

Brahms recalls PlGF Plus KRYPTOR test (REF 859075N) due to QC underestimation risk causing false preeclampsia risk classification.

Fagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.

Geri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.

Medline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.

Siemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.

Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.

Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.

Wawa recalls 16 oz Iced Tea Lemon, Diet Iced Tea Lemon, Diet Lemonade, and Fruit Punch over undeclared milk allergen.

Coluans Christmas Light-Up Rings (model SJP-50) are recalled due to a battery ingestion hazard that can cause serious injury or death.

Beestech spiral children's tower toys (Model Bee-210316-01) are recalled due to a choking hazard from small balls.

Elenker portable bed rails are recalled due to a serious entrapment and asphyxiation hazard that violates federal safety standards.

Samson International is recalling Universal Broadmoor canopy bed frames due to a collapse hazard that poses a risk of impact and injury.

Member's Mark children's pajama sets are recalled for violating federal flammability standards, posing a risk of burn injuries.

Tuymec Minoxidil Hair Growth Kits are recalled due to a lack of child-resistant packaging, posing a poisoning risk to young children.

Gavoyeat Halloween Light-Up Rings (model 43398-68657) are recalled due to a battery ingestion hazard that can cause serious injury or death.

Sangohe is recalling models 504E and 504Q adult portable bed rails due to serious entrapment and asphyxiation hazards.

Fresenius Kabi recalls 14 lots of Sodium Chloride and Dextrose Injections due to sterility concerns.

Tornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.

Medline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.

GE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.

Medtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.