glass Recalls

160 recalls tagged with “glass”.

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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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

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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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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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 DEVICE

Civco Medical eTRAX 14G Needle Sensor Recall for 5 Units (2026)

Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.

Civco Medical Instruments Co.
There was
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Food & Beverages
HIGH
FDA FOOD

Savannah Bee Company Honey BBQ Sauce Mustard Recalled for Soy and Wheat Allergens (2026)

4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.

Savannah Bee Company
Undeclared Allergens:
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs worldwide on February 18, 2026. The recall covers models SCPX-107MH, SCPX-117MH, SCPX-127MH, SCPX-135MH, SCPX-146MH and SCPX-156MH. Infusion sets may include a dull needle tip that is difficult to advance and may break. Stop using the device and follow recall instructions from the manufacturer, with recall notification by-

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Biopsy Valves in Medline Thoracic Robotic Kits Recalled for Rubber Fragments (14,379 Kits,

Olympus biopsy valves in Medline Industries, LP thoracic robotic biopsy valve kits are recalled nationwide. The recall covers 14,379 kits distributed across 13 states. Rubber fragments may detach from single-use biopsy valves, creating a risk of a foreign body in the patient’s tracheobronchial tree and possible inflammation or hypoxia. Healthcare providers and patients should stop using the device

Olympus
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed Paradigm Revel Insulin Pumps Recalled: 26,647 Units Worldwide (2026)

Medtronic MiniMed recalled 26,647 Paradigm REAL-Time Revel insulin pumps distributed worldwide, including in the United States. A design flaw can cause insulin to be over- or under-delivered when the pump height changes relative to the infusion site. Patients and health providers should stop using the device immediately and follow the manufacturer’s recall instructions. The recall covers Paradigm,

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 620G Insulin Pump Recall Impacts 799 Units Worldwide (2026)

Medtronic MiniMed recalled 799 infusion pumps worldwide, including in the United States. The devices in the Paradigm, 600, and BLE 700 series can deliver too much or too little insulin when their height relative to the infusion site changes due to gravity. Stop using the pump immediately and contact Medtronic MiniMed for instructions on replacement or refund.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Endoscope Reprocessor OER-Elite Recall Affects 2,929 Units (2026)

Olympus Corporation of the Americas is recalling 2,929 units of the OER-Elite Endoscope Reprocessor in the United States. The MAJ-1443 and MAJ-1444 modules are no longer reprocessing compatible with the OER-Pro and OER-Elite systems. Hospitals and healthcare providers should stop using the affected devices immediately and follow the recall instructions issued by Olympus.

Olympus Corporation of the Americas
The MAJ-1443
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Half Aprons Recalled for Attenuation Degradation Risk (2026)

Burlington Medical recalled 402 Half Aprons sold worldwide after potential attenuation degradation. Attenuation material Xenolite 800 may degrade over time, reducing shielding lifespan. Patients and healthcare providers should stop using the aprons immediately and contact Burlington Medical for recall instructions.

Burlington Medical
Potential for
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Food & Beverages
HIGH
FDA FOOD

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Juniper Granola recalled 1,800 Junebar Chocolate Cherry All Natural Snack Bars sold in New York after undeclared milk and soy were found. The bars carry Lot L1300 and variants L1300A and L1300B. They were produced in a facility that also processes gluten, peanuts, and sesame. Consumers should not eat these bars and should contact Juniper Granola for refunds or replacements.

Juniper Granola
Products contain
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Food & Beverages
HIGH
FDA FOOD

Hortex Mieszanka 9 Recall for Glass Contamination in 2026

1,134 units of Hortex Mieszanka 9 Spring Vegetable Mix are recalled in Illinois due to potential glass contamination. The recall involves LOT SoC1070925 and UPC 5900477018735. Consumers should stop using the product and contact Polski Ogrod Sp. z o.o. for refunds or replacements.

Polski Ogrod
potential contamination
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Tag Statistics

Total Recalls
160

Related Tags

stop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulatedimmediate actionkitchenfederal law violationburn risklaceration riskpoisoning riskinfant product