cpsc regulated Recalls

2,142 recalls tagged with “cpsc regulated”.

Recalled Bicystar High Chair - model TB-HC6900
HIGH
CPSC

Bicystar High Chairs Recalled Due to Fall and Entrapment Risks

Bicystar recalled children's high chairs on February 26, 2026, due to serious fall and entrapment hazards. The affected high chairs lack required crotch restraints, putting children at risk. Consumers should stop using these chairs immediately and seek a refund.

Bicystar High Chairs
The high
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Recalled Evajoy Above-Ground Pool Model EJ-HF032
MEDIUM
CPSC

Evajoy Pools Recalled Due to Drowning Hazard for Children

Evajoy recalled all above-ground pools 48 inches and taller on February 26, 2026, due to a drowning hazard. The recall affects models EJ-HF032, EJ-HF044, and EJ-HF045, which may allow children to access the pool using footholds. Consumers should stop using the pools and contact Evajoy for a free repair kit.

Shenzhen Danya Tech Co., Ltd.
The compression
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Recalled SumDirect LED Mini Blinking Lights
HIGH
CPSC

SumDirect LED Mini Lights Recalled Over Battery Ingestion Risk

SumDirect recalled LED mini lights on February 26, 2026, due to a serious ingestion risk from button cell batteries. The recall affects products that are easily accessible to children and lack required safety warnings. Consumers should stop using the lights immediately and seek a refund.

SumDirect LED Mini Lights
The recalled
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Recalled TheKiddoSpace Reusable Water Balloons
HIGH
CPSC

TheKiddoSpace Recalls Water Balloons Over Phthalate Risk

TheKiddoSpace recalled its reusable water balloons on February 26, 2026, due to phthalate exposure risks. The recall impacts refillable silicon balls that come with a mesh storage bag. Consumers should stop using these products immediately and contact the company for a free replacement.

TheKiddoSpace
The cord
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Recalled Grtard Magnet Men Stick Figure Toy Set
HIGH
CPSC

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.

Grtard Magnetic Stick Figure Toy Sets
The magnetic
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Health & Personal Care
HIGH
FDA DEVICE

Synthes Bone Taps Recall 33-Unit Lot Swap Causes Incorrect Threading (2026)

Synthes bone taps recalled nationwide in the United States after a lot swap affected 33 units sold through multiple retailers. The defect is an incorrect thread caused by a lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8. Healthcare providers should stop using these devices immediately and follow recall instructions from Synthes.

Synthes
A full
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Everest Bipolar Cutting Forceps 3005 Recalled for Jaw Break Risk in 2026

Olympus Corporation of the Americas is recalling 106 Everest Bipolar Cutting Forceps worldwide. The devices can have welding defects that may cause the jaw to break during use. Stop using immediately and contact Olympus or your healthcare provider for instructions.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus HALO PKS Cutting Forceps HACF0533 Recalled for Jaw Breakage; 2,648 Units Worldwide (2026)

Olympus Corporation of the Americas is recalling 2,648 HALO PKS Cutting Forceps HACF0533 sold to hospitals and clinics worldwide. The jaw can break during surgical use due to a supplier welding-validation issue. Healthcare facilities should stop using the device immediately and follow Olympus recall instructions for disposition.

Olympus Corporation of the Americas
Olympus identified
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Health & Personal Care
HIGH
FDA DEVICE

Olympus PKS Cutting Forceps 920005PK Recalled for Jaw Break Risk (2026)

Olympus Corporation of the Americas recalled 326 PKS Cutting Forceps worldwide. The devices may have welding defects that cause the jaw to break during use. Stop using the device immediately and follow the recall instructions provided by Olympus.

Olympus Corporation of the Americas
Olympus identified
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Food & Beverages
HIGH
FDA FOOD

Novamex Coconut Water Recall Targets 12,000 Cases Over Packaging Nutrition Facts Discrepancy

A Tipp Distributors, Inc. dba Novamex recall affects 12,000 cases of C2O Coconut Water with Pulp sold across multiple states. The outer cardboard box lists an incorrect Nutrition Facts Panel and Ingredient List, omitting added sugar. The can itself has the correct information. Consumers should avoid consumption and seek refund or replacement.

Novamex
The outer
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Food & Beverages
HIGH
FDA FOOD

King Harvest Balsamic Hummus Recalled for Aluminum Shards in 326 10oz Tubs (2026)

King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Fresh CO Recalls King Harvest Spinach Hummus 2026 for Aluminum Fragments

Pacific Coast Fresh CO is recalling 239 containers of King Harvest Spinach Hummus sold in Oregon and Washington. Each 10-ounce tub bears UPC 025726311087 and Best By date 2/27/2026. Stop using the product immediately due to aluminum fragments and call Pacific Coast Fresh CO by telephone for refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Food & Beverages
HIGH
FDA FOOD

King Harvest Black Olive Hummus Recalled for Aluminum Pieces in 319 Containers (2026)

King Harvest Black Olive Hummus, sold in 10-ounce plastic tubs and distributed in Oregon and Washington, is recalled after aluminum fragments were found. The recall cites a foreign material hazard. Consumers who purchased it should not consume it and should contact Pacific Coast Fresh CO by telephone for a refund or replacement.

Pacific Coast Fresh CO
Foreign material
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Atellica CH A1c_E Recall for 21,291 Units (2026)

Siemens Healthcare Diagnostics recalled 21,291 Atellica CH A1c_E units distributed to laboratories nationwide and internationally in 2026. The recall addresses a depressed result bias when A1c_E is processed with RCRP on the same analyzer. Labs using separate analyzers are not impacted. Stop using the affected module immediately and follow manufacturer instructions. Contact Siemens or your lab’s F

Siemens Healthcare Diagnostics
A potential
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