HIGH
FDA DRUG
HydroPeptide CLEAR ALLIANCE SERUM, 2.5% BENZOYL PEROXIDE, a)1 FL OZ/30ml; b) 2 FL OZ/60ml spray bottle; DIST BY HYDROPEPTIDE LLC, ISSAQUAH, WA 98027
Chemical contamination: Presence of benzene
Owen Biosciences
Chemical contamination:
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
High Risk Recalls
3,609 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
What to do if you own a recalled product:
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
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
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
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
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
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
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
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
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
Health & Personal Care
HIGH
FDA DRUG
Leader Artificial Tears Recalled 589,848 Bottles for Sterility Issue in 2026
Leader Artificial Tears Sterile Lubricant Eye Drops sold nationwide are recalled due to lack of assurance of sterility. The recall involves multiple store-brand lines distributed by Cardinal Health and others. Consumers should stop using the product immediately and follow recall guidance from KC Pharmaceuticals via email.
Leader
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 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
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
HIGH
FDA DEVICE
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Wilson-Cook Medical
Due to
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
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10F Recall for 10 Units Worldwide (2026)
Philips Medical Systems Nederland B.V. recalls 10 Allura Xper FD10F imaging systems sold to hospitals worldwide. The devices may fail to start X-ray imaging or start intermittently when using the wired foot switch. Hospitals should stop using the devices immediately and contact Philips for instructions.
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 Medical Systems Nederland B.V. recalled 196 ALLURA Xper FD20 OR Tables sold to hospitals nationwide and internationally. The defect may prevent X-ray imaging from starting or cause intermittent operation when using the wired foot switch. Hospitals should stop using the devices and follow the recall instructions sent by letter.
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 is recalling 798 Azurion 3 M15 systems worldwide, including 42 units in the United States. The wired foot switch may fail to initiate X-ray imaging or fail to produce consistent imaging. Healthcare providers should stop using the affected devices and follow recall instructions issued by Philips.
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 recalled 1,994 Azurion 7 M12 interventional X-ray systems, including 360 units in the United States, for a wiring-foot switch defect that may fail to initiate imaging. The issue can cause imaging to not start or operate intermittently. Hospitals and clinicians should stop using affected devices immediately and follow the manufacturer’s recall instructions.
Philips
Philips has
Health & Personal Care
HIGH
FDA DEVICE
Philips Azurion 7 B12 X-ray System Recalled for Foot Switch Imaging Failure (670 Units, 2026)
Philips recalls 670 Azurion 7 B12 X-ray imaging systems after finding the wired foot switch may fail to start imaging. The issue affects 106 US units and 564 in other countries. Hospitals should stop using the device and await manufacturer guidance.
PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
HIGH
FDA DEVICE
AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Catalog No.: 13709604; Product/UPN No.: H787137096045...
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics
The affected
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