stop use immediately Recalls

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

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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/15 OR Table Recall for 8 Units Worldwide in 2026

Philips Medical Systems Nederland B.V. recalls 8 Allura Xper FD20/15 OR Tables worldwide due to a risk that X-ray imaging may not start or may stop intermittently when using the wired foot switch. The issue is tied to System Code 722059 and requires immediate action. Hospitals and patients should stop using the device and follow the manufacturer’s recall instructions.

Philips
Philips has
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
Health & Personal Care
HIGH
FDA DRUG

Goodsense Eye Drops Original Formula Recall 378,144 Bottles Nationwide 2026

Goodsense Eye Drops Original Formula, distributed nationwide, has recalled 378,144 sterile bottles in 2026 due to lack of assurance of sterility. The sterile ophthalmic solution may be contaminated. Consumers and healthcare providers should stop using immediately and contact K.C. Pharmaceuticals for refunds or replacements.

Goodsense Eye Drops Original Formula
Lack of
Read more
Health & Personal Care
HIGH
FDA DRUG

LEADER Ultra Lubricating Eye Drops Recalled for Sterility Issue (2026)

Cardinal Health distributed LEADER Ultra Lubricating Eye Drops and related store-brand lubricating eye drops nationwide. The recall cites a lack of assurance of sterility. Consumers should stop using these products immediately and contact KC Pharmaceuticals for guidance.

LEADER ULTRA LUBRICATING EYE DROPS
Lack of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland recall 296 Allura Xper FD20/15 Imaging Systems Over Foot Switch Fl

Philips Medical Systems Nederland B.V. recalls 296 Allura Xper FD20/15 imaging systems distributed nationwide and internationally after reports the wired foot switch may fail to initiate imaging or start intermittently. The defect can delay X-ray imaging in patient care. Healthcare providers and patients should stop using the device and follow recall instructions from the manufacturer.

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

Philips Allura Xper FD20/20 OR Table Recalled for Intermittent X-ray Activation (2026)

Philips Medical Systems Nederland B.V. recalled 5 Allura Xper FD20/20 OR Tables distributed nationwide and internationally after detecting intermittent X-ray activation with the wired foot switch. The defect can prevent X-ray imaging from starting or cause it to stop during procedures. Hospitals and clinicians should stop using the affected tables and await manufacturer guidance.

Philips Medical Systems Nederland
Philips has
Read more
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
Read more
Previous
12345...94
Next

Tag Statistics

Total Recalls
1,862

Related Tags

glassreturn for refundreplacement availablefda regulatedcpsc regulatedimmediate actionkitchenfederal law violationburn risklaceration riskpoisoning riskinfant product