Food & Beverages
HIGH
FDA FOOD
Ajinomoto Kroger Chinese Inspiration Fried Rice Recalled for Glass Contamination (2026)
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Ajinomoto Foods North America
Foreign objects
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 5 M20 Recall: 920 Imaging Systems Worldwide Affected (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Food & Beverages
HIGH
FDA FOOD
Ajinomoto Green Gyoza Dumplings Recalled for Glass Shards in 537,033 Lbs (2026)
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Ajinomoto Foods North America
Foreign objects
Food & Beverages
HIGH
FDA FOOD
Ajinomoto Ling Ling Restaurant Style Fried Rice Recall: 3,780 Cases Glass Fragments (2026)
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Ajinomoto Foods North America
Foreign objects
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/15 OR Table Recall for 8 Units Worldwide in 2026
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Biplane Recalled for Intermittent X-Ray Imaging (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips
Philips has
Health & Personal Care
HIGH
FDA DRUG
KC Pharmaceuticals Sterile Eye Drops Soothing Tears Recall 74,016 Bottles (2026)
Lack of Assurance of Sterility
KC Pharmaceuticals
Lack of
Health & Personal Care
HIGH
FDA DRUG
Quality Choice Eye Drops and Foster & Thrive Eye Drops Recalled for Sterility in 303,216 Bottles (24
Lack of Assurance of Sterility
Quality Choice
Lack of
Health & Personal Care
HIGH
FDA DRUG
K.C. Pharmaceuticals Sterile Eye Drops Recall 315,144 Bottles for Lack of Sterility (2026)
Lack of Assurance of Sterility
GNP Eye Drops Redness and Dry Eye Relief
Lack of
Health & Personal Care
HIGH
FDA DRUG
ARTIFICIAL TEARS Dry Eye Relief Eye Drops Recalled in 2026 Over Sterility Concerns
Lack of Assurance of Sterility
ARTIFICIAL TEARS
Lack of
Health & Personal Care
HIGH
FDA DRUG
Goodsense Eye Drops Original Formula Recall 378,144 Bottles Nationwide 2026
Lack of Assurance of Sterility
Goodsense Eye Drops Original Formula
Lack of
Health & Personal Care
HIGH
FDA DRUG
LEADER Ultra Lubricating Eye Drops Recalled for Sterility Issue (2026)
Lack of Assurance of Sterility
LEADER ULTRA LUBRICATING EYE DROPS
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland recall 296 Allura Xper FD20/15 Imaging Systems Over Foot Switch Fl
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 OR Table Recalled for Intermittent X-ray Activation (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10C X-ray System Recall for 15 Units Worldwide (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10F Recall for 10 Units Worldwide (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips ALLURA Xper FD20 OR Table Recalled Worldwide; 196 Units Affected (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 3 M15 Recall for 798 Units Worldwide Over Intermittent X-ray Imaging (2026)
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips Medical Systems Nederland
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 7 M12 Recall 2026 for Intermittent X-ray Imaging in 1994 Units
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips
Philips has
Tag Statistics
Total Recalls
2,229