All Recalls

Evajoy above-ground pools are being recalled due to a drowning hazard caused by a compression strap that can act as a foothold for children.

Grtard magnetic stick figure toy sets are recalled due to a serious magnet ingestion hazard that can cause severe injury or death in children.

Bicystar is recalling gray high chairs due to fall and entrapment hazards caused by a missing crotch restraint.

Vevor is recalling safety gates (models YJ-3355, YJ-3371, YJ-33110) due to an entrapment hazard that violates federal safety standards.

Joyreal busy board toys are recalled due to choking and laceration hazards from a detachable, sharp-edged mirror.

Dupray is recalling Neat Steam Cleaners due to a boiler rupture risk that can cause burns or serious injury.

Somgem pig-shaped and Yomin toilet-shaped lighters are recalled for lacking mandatory child-resistant mechanisms, posing fire and burn risks.

PQL is recalling various 2-foot and 4-foot High Bay Linear LED light fixtures due to a fire hazard from loose internal LED boards.

TheKiddoSpace children's flashcard toys are recalled due to toxic lead and phthalate levels and a battery short circuit hazard.

TheKiddoSpace is recalling children's handwriting practice kits because the included pens contain lead levels exceeding federal safety limits.

TheKiddoSpace is recalling children's fabric story books due to a choking hazard from detachable felt parts.

KiddoSpace fingerpainting kits are recalled due to toxic methanol, ethylene glycol, and phthalate content.

TheKiddoSpace sensory swings are recalled due to a strangulation hazard posed by the fabric forming loops that can entangle a child.

TheKiddoSpace Montessori egg puzzle toys are recalled due to a choking and suffocation hazard for children under three.

SumDirect LED mini lights are recalled due to a serious battery ingestion hazard and lack of required safety warnings.

TheKiddoSpace children's Christmas tree play sets are recalled due to lead exposure risk and failure to meet federal toy safety standards.

Tubby Tots Fizzy Flask bath foam sets (batch 082025) are recalled due to an impact hazard from pressure buildup in the containers.

Trankerloop baby bath seats are recalled due to a drowning hazard, as they are unstable and can tip over during use.

Magnetic chess games are recalled due to a serious magnet ingestion hazard that can cause severe internal injuries or death in children.

TheKiddoSpace peg doll toys are recalled due to a choking hazard that violates the federal small parts ban for children under three.

TheKiddoSpace is recalling reusable water balloons because the storage bag cord locks contain a regulated phthalate, violating a federal ban.

Zelbuck children's chess games (model 999-9) are recalled due to a serious magnet ingestion hazard that can cause severe injury or death.

Concord 360 Degree Rechargeable Light-Up bike helmets are recalled for failing to meet federal safety standards, posing a head injury risk.

Teva recalls Metoprolol Succinate ER tablets (25-200 mg) over failed dissolution specs.

Abiomed recalls Impella RP Flex with SmartAssist due to sensor drift risk.

Roche is recalling Cobas Pro analytical units due to a software defect that can cause the system to report erroneous, repeated test results.

GE Healthcare is recalling Centricity Universal Viewer software due to a risk of patient information and image mismatch.

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

Remel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.

Agiliti is recalling the Adapt Pump (model 61600200) for a software failure that prevents the Microclimate Management function from restarting.

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

Medline is recalling kits containing Tego Connectors due to potential silicone seal defects that may cause fluid leakage or therapy delays.

Encore Medical is recalling EMPOWR 3D Knee and RSP Humeral Socket implants due to incorrect labeling.

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

Slate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.

AvKARE is recalling Amantadine HCl Capsules 100 mg (NDC 50268-069-15) nationwide due to failed dissolution specifications.

LEO Pharma is recalling Adbry (tralokinumab-ldrm) injection due to a lack of sterility assurance following the discovery of wool fiber.

Gerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.

JJGoo LED balloon lights (Model MY1005E-Colorfu1-100) are recalled due to a serious battery ingestion and chemical burn hazard to children.

Huaker magnetic toy building sets (Model 20A-13) are recalled due to a serious choking hazard from small balls.

Joly's 80% Vinegar is recalled for missing mandatory safety labels, posing risks of poisoning and chemical burns.

Prismatic 3D Prints is recalling Book Nooks because their spare coin batteries are easily accessible, posing a serious ingestion hazard.

Vive Health is recalling models LVA1024 and LVA3031BLK bed rails due to a serious entrapment and asphyxiation risk.

SAMIT youth multi-purpose helmets are recalled for failing federal safety standards, posing a risk of serious head injury or death.

Domino Foods recalls Sodexo Stars Saccharin Packets due to undeclared aspartame.

Kirkland Signature Mini Beignets are recalled due to undeclared hazelnut, which poses a risk to consumers with allergies.

Accord BioPharma is recalling Udenyca injection due to improper storage temperature conditions.

American Health Packaging is recalling Oxycodone 5 mg tablets due to defective blister card seals that may cause tablets to fall out.

Meitheal Pharmaceuticals is recalling Cetrorelix Acetate injection kits due to missing or duplicated needles in the delivery system.

Olympus is recalling the UHI-3 High Flow Insufflation Unit due to a software issue that may cause dangerous overpressure events.