cpsc regulated Recalls

1,716 recalls tagged with “cpsc regulated”.

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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Food & Beverages
HIGH
FDA FOOD

Ajinomoto recalls 3.86 million pounds of Teppanyaki Style Vegetable Fried Rice over glass in 2026

Ajinomoto Foods North America recalled 3,862,944 pounds of Ajinomoto Teppanyaki Style Vegetable Fried Rice distributed nationwide in 2026. Glass fragments measuring 1 to 3 cm long and 2 to 4 mm wide were found in the frozen product. Consumers should not eat this product and should contact Ajinomoto Foods North America for refund or replacement, using the recall details listed on the FDA page and a

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

Ajinomoto Foods North America Recalls 35,955 Pounds of Japanese-Style Fried Rice for Glass Contamin‑

Ajinomoto Foods North America recalled 35,955 pounds of Ajinomoto Japanese-Style Vegetable Fried Rice distributed by multiple retailers in 43 states after glass fragments were found in the product. The glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers who bought the product should not eat it 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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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Vegetable Gyoza Dumplings Recalled for Glass Contaminants in 36,682 lbs (2026)

Ajinomoto Foods North America recalled 36,682 pounds of Vegetable Gyoza Dumplings distributed nationwide after glass fragments were detected in frozen products. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the 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 Azurion 5 M20 Recall: 920 Imaging Systems Worldwide Affected (2026)

Philips Medical Systems Nederland B.V. recalled 920 Azurion 5 M20 imaging systems worldwide, including 168 in the United States. The recall cites a defect in which X-ray imaging may not start or may begin intermittently when using the wired foot switch. Healthcare providers should stop using the device immediately and await instructions from Philips.

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

Ajinomoto Green Gyoza Dumplings Recalled for Glass Shards in 537,033 Lbs (2026)

Ajinomoto Foods North America recalls 537,033 pounds of Ajinomoto Green Gyoza Vegetable & Edamame Dumplings sold nationwide after glass fragments were found. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the recalled dumplings and should contact Ajinomoto Foods North America for a refund or replacement.

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

Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)

Philips Medical Systems Nederland B.V. recalls 111 Allura Xper FD20/20 imaging systems with System Code 722038. The recall covers 31 units in the United States and 80 abroad. The defect may prevent X-ray imaging from starting or cause intermittent imaging when using the wired foot switch. Stop using the device immediately and follow recall instructions from Philips or your healthcare provider.

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 DRUG

KC Pharmaceuticals Sterile Eye Drops Soothing Tears Recall 74,016 Bottles (2026)

KC Pharmaceuticals recalls 74,016 bottles of Sterile Eye Drops Soothing Tears distributed nationwide by Rugby Laboratories and Walgreens. The recall cites a lack of assurance of sterility. Consumers and healthcare providers should stop using the product immediately and contact KC Pharmaceuticals for guidance.

KC Pharmaceuticals
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Quality Choice Eye Drops and Foster & Thrive Eye Drops Recalled for Sterility in 303,216 Bottles (24

Quality Choice Moisturizing Relief Eye Drops and Foster & Thrive Advanced Relief Eye Drops are recalled after 303,216 bottles distributed nationwide through Walgreens, CVS and other retailers lack sterility. The defect is lack of assurance of sterility. Consumers should stop using the products immediately and contact KC Pharmaceuticals for guidance.

Quality Choice
Lack of
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Health & Personal Care
HIGH
FDA DRUG

K.C. Pharmaceuticals Sterile Eye Drops Recall 315,144 Bottles for Lack of Sterility (2026)

K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider

GNP Eye Drops Redness and Dry Eye Relief
Lack of
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Health & Personal Care
HIGH
FDA DRUG

ARTIFICIAL TEARS Dry Eye Relief Eye Drops Recalled in 2026 Over Sterility Concerns

More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s

ARTIFICIAL TEARS
Lack of
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Tag Statistics

Total Recalls
1,716

Related Tags

electrical hazardstop use immediatelyreturn for refundimmediate actionmandatory standard violationfda regulatednhtsa regulatedtip over riskburn riskinfant productadult productreplacement available