Recall database
All Product Recalls
- Active recalls
- 4,441
- Current page
- 84

Surreal Brands Recalls Tubby Tots Bath Foam Sets Over Impact Hazard
Surreal Brands recalled Tubby Tots Fizzy Flask Bath Magic bath foam sets on February 26, 2026. Moisture can cause pressure to build up, posing an impact hazard. Consumers should stop using these products immediately and seek a refund.


TheKiddoSpace Recalls Sensory Swing Over Strangulation Risk
TheKiddoSpace recalled its sensory swings on February 26, 2026. The swings pose a high risk of serious injury or death from strangulation. Consumers should stop using the swings immediately and seek a refund.

Somgem and Yomin Toilet Lighters Recalled for Fire Hazard
Somgem and Yomin recalled pig and toilet lighters on February 26, 2026. The lighters lack child-resistant features, posing serious burn risks. Consumers should stop using these products immediately and seek refunds.

Evajoy Pools Recalled Due to Drowning Hazard for Children

TheKiddoSpace Recalls Handwriting Kits Due to Lead Hazard
TheKiddoSpace recalled children’s handwriting practice kits on February 26, 2026. The kits contain pens with lead levels exceeding federal limits. This poses a risk of lead exposure to young children.

Grtard Magnetic Stick Figures Recalled Due to Magnet Hazard
Grtard recalled magnetic stick figure toy sets on February 26, 2026. The toys pose a serious risk of injury or death from magnet ingestion. Consumers should stop using the toys immediately and seek a refund.


Joyreal Busy Board Toys Recalled Over Choking and Laceration Hazards
Joyreal recalled busy board toys on February 26, 2026, due to choking and laceration hazards. The toys can have small parts that pose serious risks to children. Consumers must stop using these toys immediately and seek refunds.

Trankerloop Baby Bath Seats Recalled Due to Drowning Risk
Trankerloop recalled baby bath seats on February 26, 2026. The seats pose a drowning risk due to instability. Consumers should stop using them immediately and seek a refund.


SumDirect LED Mini Lights Recalled Over Battery Ingestion Risk
This recall involves SumDirect-branded LED mini lights. The recalled blinking lights rotate and have a built-in loop for hanging. Each of the 24 multicolored lights includes three preinstalled LR41 button cell batteries.
WeiKFiELD Custard Powder Kesar Pista, Net Wt. 300g (10.6 OZ.), Poly Jar , 24 units per outer case.
The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.
Novamex Coconut Water Recall Targets 12,000 Cases Over Packaging Nutrition Facts Discrepancy
Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB; 2) MANIFOLD KIT LOW PRESSURE OFF, Model Number: VASCSLPOFF1; 3) EP MANIFOLD KIT, Model Number: VASC1018A
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Namic Syringes: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB;
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF, Model Number: DYNJT2164M; 4) ANGIOGRAPHY TRAY, Model Number: DYNJT3078; 5)...
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Kits: 1) HYSTEROSCOPY PACK, Model Number: DYNJ48399C; 2) SLING PACK, Model Number: DYNJ62849B
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.