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
Category hub
Health & Personal Care Recalls
1,882 product recalls found in this category. Browse active safety alerts and related categories from the same official source network.
- Active recalls
- 1,882
- Pages
- 95
High activity category
This category has a significant number of recalls. Check it regularly if you own products in this area.
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 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 ALLURA Xper FD20 Recall for 5,084 Units 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 B.V.
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems 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 MEDICAL SYSTEMS NEDERLAND
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 7 M20 X-ray System Recall Affects 5,167 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
Philips has
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 Azurion 5 M12 X-ray System Recall 2026: 345 Worldwide Units Affected
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 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
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 7 B20 Interventional X-ray System Recall for 1,523 Units (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
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 DEVICE
Philips Azurion 3 M12 Recall for Intermittent X-ray Imaging (298 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 Biplane OR Table Recall for 4 Units Over Intermittent X-ray Activation (202
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 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 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 DEVICE
Oxoid Microbact 12L Kit 20 Tests Recalled for Misidentification Risk (2026)
Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells.
Oxoid
Oxoid Ltd.,
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 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
Civco Medical Instruments Recalls 10 eTRAX Needle Sensor 16G for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments
There was
Health & Personal Care
HIGH
FDA DEVICE
Civco Medical Instruments Recalls 2 eTRAX 12G Starter Kits for Aurora Trackers (2026)
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
Civco Medical Instruments
There was
Related Categories
Category Statistics
Total Recalls
1,882
Pages
95