stop use immediately Recalls

1,862 recalls tagged with “stop use immediately”.

Food & Beverages
HIGH
FDA FOOD

JFE FRANCHISING INC Dumpling Vegetable and Loaded Dumpling Vegetable Recalled for Glass (2 SKUs, 202

JFE FRANCHISING INC recalled two dumpling products sold at retailers nationwide: Dumpling Vegetable 4.5 oz (UPC 011110658067) and Loaded Dumpling Vegetable 5.7 oz (UPC 011110696953) due to a glass contamination risk. The recall is Class II with a high hazard level. Consumers should not eat the dumplings and should contact JFE FRANCHISING INC by email for refund or replacement.

JFE FRANCHISING
Foreign Object
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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 HALO Magic Sleepsuit
HIGH
CPSC

HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard

HALO Dream recalled its Magic Sleepsuit on March 5, 2026, after discovering a choking hazard. The recall affects specific batch codes PO30592, PO30641, and PO30685. Parents should immediately stop using these sleepsuits and seek a refund or replacement.

HALO Dream
The zipper
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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

Trader Joe's Vegetable Fried Rice Recalled for Glass Fragments in 9.9 Million Pounds (2026)

Ajinomoto Foods North America recalled Trader Joe's Vegetable Fried Rice sold at Trader Joe's nationwide after glass fragments were found in the product. The contamination involves glass shards ranging from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should contact Ajinomoto Foods North America for refunds or replacements.

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

Philips Azurion 5 M12 X-ray System Recall 2026: 345 Worldwide Units Affected

Philips Medical Systems Nederland B.V. recalled 345 Azurion 5 M12 X-ray systems distributed worldwide after reports that X-ray imaging may not start or may run intermittently when using the wired foot switch. The defect could affect imaging during patient care. Hospitals should stop using the device immediately and follow the recall instructions in the notification letter.

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

Oxoid Microbact 12L Kit 20 Tests Recalled for Misidentification Risk (2026)

Oxoid recalled 2 Microbact 12L Kit 20 Tests MB1128A lot 4494873 distributed nationwide in the United States, including Georgia and California. The kit may identify the wrong organism due to inconclusive color reactions in wells. Laboratories should stop using the kit immediately and follow recall instructions from Oxoid.

Oxoid
Oxoid Ltd.,
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Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 B20 Interventional X-ray System Recall for 1,523 Units (2026)

Philips Medical Systems Nederland B.V. recalls 1,523 Azurion 7 B20 interventional X-ray systems used by hospitals nationwide after possible failure to initiate X-ray imaging. The defect affects whether imaging starts when using the wired foot switch. Hospitals should stop using the device and follow Philips recall instructions immediately.

Philips
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20 Biplane OR Table Recall for 4 Units Over Intermittent X-ray Activation (202

Philips Medical Systems Nederland B.V. recalls 4 units of the Allura Xper FD20 Biplane OR Table after identifying intermittent or failed X-ray initiation when using the wired foot switch. The recall covers System Codes 722020 and 722025. Healthcare facilities were notified by letter. Stop using the affected devices and follow Philips instructions.

Philips Medical Systems Nederland
Philips has
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Foods North America Recalls 3,059,808 Lbs Trader Joe's Fried Rice For Glass Contamination

Ajinomoto Foods North America recalls 3,059,808 pounds of Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed sold nationwide after glass fragments were found in the product. The glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the product and should seek a refund or replacement. The recall number is H-0591-2026.

Ajinomoto Foods North America
Foreign objects
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Tai Pei Shrimp Fried Rice Recalled for Glass Shards in 9,913 Cases (2026)

Ajinomoto Foods North America recalled 9,913 cases distributed nationwide after glass fragments were found in Tai Pei Shrimp Fried Rice. The glass pieces measure 1-3 cm long and 2-4 mm wide. Consumers should not eat the product and should contact Ajinomoto for refund or replacement information.

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

Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems in 2026

Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
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Tag Statistics

Total Recalls
1,862

Related Tags

laceration riskimmediate actionreturn for refundreplacement availablefda regulatedelectrical hazardcpsc regulatednhtsa regulatedpet relatedkitchenfederal law violationglass