replacement available Recalls

280 recalls tagged with “replacement available”.

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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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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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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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 Kroger Chinese Inspiration Fried Rice Recalled for Glass Contamination (2026)

Ajinomoto Foods North America recalled 109,741 cases of Kroger Chinese Inspiration Vegetable Fried Rice sold at Kroger stores after glass fragments were found. Glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should seek a refund or replacement from Ajinomoto Foods North America.

Ajinomoto Foods North America
Foreign objects
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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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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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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 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 Azurion 7 M12 Recall 2026 for Intermittent X-ray Imaging in 1994 Units

Philips recalled 1,994 Azurion 7 M12 interventional X-ray systems, including 360 units in the United States, for a wiring-foot switch defect that may fail to initiate imaging. The issue can cause imaging to not start or operate intermittently. Hospitals and clinicians should stop using affected devices immediately and follow the manufacturer’s recall instructions.

Philips
Philips has
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Ling Ling Restaurant Style Fried Rice Recall: 3,780 Cases Glass Fragments (2026)

Ajinomoto Foods North America recalled 24,796 pounds of Ling Ling Restaurant Style Fried Rice Savory Vegetable sold in multiple states. Glass fragments were found in the product and measure 1–3 cm long and 2–4 mm wide. Consumers should not eat the product and should contact Ajinomoto Foods North America for a refund or replacement.

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

Ajinomoto Vegetable Gyoza Dumplings 12ct Recalled for Glass Shards (2026)

Ajinomoto Foods North America recalled 8,097 cases of Ajinomoto Vegetable Gyoza Dumplings sold nationwide through retailers. Glass fragments measuring 1 to 3 cm long and 2 to 4 mm wide were found in the product. Consumers should not eat the dumplings and should contact Ajinomoto Foods North America for refund or replacement.

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

Philips Allura Xper FD10C X-ray System Recall for 15 Units Worldwide (2026)

Philips Medical Systems Nederland B.V. recalled 15 Allura Xper FD10C radiography systems worldwide, including 7 in the United States and 8 overseas. The devices may fail to initiate X-ray imaging or intermittently stop imaging when using the wired foot switch. Facilities should stop using the devices and await recall instructions from Philips.

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

Philips Allura Xper FD20 Biplane Recalled for Intermittent X-Ray Imaging (2026)

Philips Medical Systems Nederland B.V. recalled 461 Allura Xper FD20 Biplanes sold to healthcare facilities nationwide and internationally. X-ray imaging may not initiate or may occur intermittently when using the wired foot switch. Hospitals should stop using the devices immediately and follow Philips’ recall instructions.

Philips
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD10F Recall for 10 Units Worldwide (2026)

Philips Medical Systems Nederland B.V. recalls 10 Allura Xper FD10F imaging systems sold to hospitals worldwide. The devices may fail to start X-ray imaging or start intermittently when using the wired foot switch. Hospitals should stop using the devices immediately and contact Philips for instructions.

Philips Medical Systems Nederland B.V.
Philips has
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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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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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