cpsc regulated Recalls

1,716 recalls tagged with “cpsc regulated”.

Food & Beverages
HIGH
FDA FOOD

POCAS International Recalls Popping Boba RTD Mango Passion Fruit Green Tea 12 x 13.8 oz (2026)

Pocas International recalled 517 cases of Popping Boba RTD Mango Passion Fruit Green Tea distributed to NY, VA, FL, MA, TX, LA, UT, CA and Canada. A packaging integrity issue may compromise product quality. Consumers who purchased it should not consume the beverage and should contact Pocas International for refund or replacement via email.

Pocas International
Packaging integrity
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Recalled 17 Stories Furniture 14-Drawer Dresser (front)
HIGH
CPSC

17 Stories Furniture Dressers Recalled Over Tip-Over Risk

17 Stories Furniture recalled its 14-drawer dressers on March 12, 2026, due to serious tip-over hazards. The dressers, sold in black, white, and brown, can pose risks of injury or death to children if not anchored. Model numbers include 55SCDR14KDBRDL and 55SCDR14KDCHDL.

Online at Wayfair.com from September 2023 through January 2026 for about $135.
The recalled
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Recalled LIVEHOM 11-Drawer Dresser – brown
HIGH
CPSC

LIVEHOM Dressers Recalled Over Tip-Over Hazard Risk

LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.

LIVEHOM 11-Drawer Dressers
The recalled
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Recalled Toddler Bike Helmet
HIGH
CPSC

ProRider Recalls Bicycle Helmets Over Serious Head Injury Risk

ProRider recalled several models of bicycle helmets on March 12, 2026, due to a serious risk of head injury. The helmets do not meet mandatory safety standards and can fail in a crash. Consumers should stop using these helmets immediately and seek a refund.

ProRider
The recalled
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Recalled Kluster Fun Tabletop Magnet Chess Game (Sold in White Pouch)
HIGH
CPSC

Stoney Games Recalls Kluster Magnet Chess Games Over Ingestion Risk

Stoney Games recalled Kluster Fun Tabletop Magnet Chess Games on March 12, 2026, due to a serious ingestion hazard. The games contain loose, high-powered magnets that can be swallowed by children, posing a risk of severe injury or death. Consumers should immediately stop using the games and contact Stoney Games for replacement options.

Stoney Games
The recalled
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Food & Beverages
HIGH
FDA FOOD

Lone Star Dairy Products Recalls 1.79M Lbs Spray Dried Dairy Powder Over Salmonella Risk (2026)

Lone Star Dairy Products LLC issued an active recall of 1.79 million pounds of spray dried dairy powder sold in the United States after Salmonella spp. was identified in finished product testing. The affected product is packaged in 25 kg bags or 1 metric ton totes. Consumers should not consume the product and should contact Lone Star Dairy Products LLC for refund or replacement information via e‑m

Lone Star Dairy Products
Salmonella spp.
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Food & Beverages
HIGH
FDA FOOD

Nuts.com Espresso Malted Milk Balls Recalled for Undeclared Wheat and Soy (2026)

Nuts.com recalled 10,190 pounds of Espresso Malted Milk Balls distributed nationwide in the United States. The recall cites undeclared wheat and soy allergens from soy lecithin in the ingredient statement. Consumers who bought this product should not consume it and should contact Nuts.com for a refund or replacement via email.

Nuts.com
Undeclared Allergen
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Health & Personal Care
HIGH
FDA DEVICE

Philips Vue Motion V12 Recall for 3,552 Units Over Cine Frame Sequencing Error (2026)

Philips Medical Systems Nederland B.V. recalled 3,552 Vue Motion V12 devices worldwide, including the United States. The recall is due to a potential that mis-ordered frames during dynamic cine runs may display out of sequence. Stop using the device and follow the recall instructions provided by the manufacturer.

Philips Medical Systems Nederland B.V.
Potential that
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Food & Beverages
HIGH
FDA FOOD

JFE Franchising Dumpling Party Tray Recall for Glass Contamination (2026)

JFE Franchising Inc. recalls Dumpling Party Tray products and a Cheetos Flamin Hot Loaded Dumpling item after glass fragments were found in the trays. The FDA enforcement report lists glass as the foreign object hazard. Consumers should not eat these products and should seek refunds or replacements via email.

JFE Franchising
Foreign Object
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Recalled Cubimana Pirate Ship Building Set box with model number (front)
HIGH
CPSC

Cubimana Island Storm Building Sets Recalled Over Battery Ingestion Risk

Cubimana recalled its Island Storm 3 In 1 Building Sets on March 5, 2026, due to a risk of serious injury or death from battery ingestion. The sets violate safety standards as they contain accessible button cell batteries. Consumers should stop using and return the product immediately for a full refund.

Cubimana Island Storm 3 In 1 Building Sets
T The
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Health & Personal Care
HIGH
FDA DEVICE

Koven Technology BiDop 3 Pocket Doppler ES-100V3 Recalled for Fetal Labeling Issue (2026)

Koven Technology recalled 34 BiDop 3 Pocket Dopplers with BT2M20S8C fetal probes nationwide after regulators found the fetal indication on the labeling was not cleared under 510(k). The defect is labeling that misrepresents fetal use. Healthcare providers and patients should stop using the devices and follow recall instructions from the manufacturer.

Koven Technology
Product labeling
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Golden Tiger Vegetable Fried Rice Recalled for Glass Contamination (2026)

Ajinomoto Foods North America recalls Ajinomoto Golden Tiger Vegetable Fried Rice sold at multiple retailers nationwide. Glass fragments measuring 1-3 cm long and 2-4 mm wide have been found in frozen rice. Consumers should not eat the product and should contact Ajinomoto for refunds or replacements.

Ajinomoto Foods North America
Foreign objects
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 M20 X-ray System Recall Affects 5,167 Units Worldwide (2026)

Philips Medical Systems Nederland recalled 5,167 Azurion 7 M20 X-ray imaging systems sold to healthcare facilities in the U.S. and internationally. The wired foot switch can fail to initiate imaging or produce intermittent imaging. Hospitals and clinics should stop using the device and follow recall instructions from Philips, with notification by letter to affected parties.

Philips Medical Systems Nederland
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD20 Recall for 5,084 Units Over Intermittent X-ray Imaging (2026)

Philips Medical Systems Nederland B.V. recalled 5,084 ALLURA Xper FD20 imaging systems sold nationwide and internationally after finding that the wired foot switch may fail to initiate X-ray imaging or perform intermittently. The defect can delay or interrupt imaging during patient care. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD10 OR Table Recalled for Intermittent X-ray Activation (2 Units, 2026)

Philips Medical Systems Nederland B.V. recalls 2 ALLURA Xper FD10 OR Tables after reports that X-ray imaging may not start or may delay when using the wired foot switch. The defect could affect patients during imaging procedures. Healthcare providers should stop using the device and follow recall instructions from the manufacturer.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DRUG

KC Pharmaceuticals Recalled Sterile Eye Drops AC 182,424 Bottles Nationwide (2026)

KC Pharmaceuticals recalled 182,424 Sterile Eye Drops AC bottles sold nationwide under multiple brands including Quality Choice Eye Drops Irritation Relief and Goodsense Ultra Lubricant Eye Drops. The recall cites a lack of assurance of sterility. Consumers should stop using the product immediately and contact KC Pharmaceuticals for guidance.

Quality Choice Eye Drops Irritation Relief
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD10/10 Imaging System Recalled for Intermittent X-ray Activation (112 Units)

Philips recalled 112 ALLURA Xper FD10/10 imaging systems nationwide in the United States and internationally after reports that X-ray imaging may not start or may intermittently stop when using the wired foot switch. The defect affects system codes 722005, 722011, and 722027. Healthcare providers should stop using the devices and follow Philips recall instructions.

Philips Medical Systems Nederland B.V.
Philips has
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Tag Statistics

Total Recalls
1,716

Related Tags

immediate actionstop use immediatelyreturn for refundreplacement availablefda regulatedglasslaceration riskkitchenpet relatedtip over riskchildren productfabric