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

2,775 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:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
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 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
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
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
Read more
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
Read more
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
Read more
Health & Personal Care
HIGH
FDA DRUG

Rising Pharmaceuticals Temozolomide 5 mg Capsules Recall 1,200 Bottles in 2026

Rising Pharmaceuticals recalls 1,200 Temozolomide 5 mg capsules nationwide after a stability test found out-of-spec impurities. The drug is Rx-only, with NDC 16571-816-51 and lot 1TM0524003A. Stop using immediately and contact a healthcare provider for guidance.

Rising Pharmaceuticals
Failed Impurities/Degradation
Read more
Health & Personal Care
CRITICAL
FDA DEVICE

Philips Respironics Trilogy Evo O2 Ventilator Recall Covers 113,717 Units Worldwide (2026)

Philips Respironics recalled 113,717 Trilogy Evo O2 home-use ventilators worldwide on March 2, 2026 after determining that using non-pneumatic nebulizers with the device can cause a mismatch between the set tidal volume and the delivered tidal volume. The defect could lead to under- or over-ventilation with serious health consequences. Stop using the device immediately and follow the recall steps.

Philips Respironics
Using non-pneumatic
Read more
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
Read more
Health & Personal Care
HIGH
FDA DEVICE

Civco Medical Instruments eTRAX Needle System Starter Kit 16G Recall for 18 Units (2026)

Civco Medical Instruments recalled 18 units of the eTRAX Needle System Starter Kit 16G for Aurora Trackers after an inspection and programming error could cause the needle tip position to be misidentified on the user interface. The defect could lead to incorrect needle guidance during a procedure. Healthcare providers and patients should stop using the device immediately and follow the recall ins

Civco Medical Instruments Co.
There was
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy Evo Ventilators Recalled for Tidal-Volume Mismatch (113,717 Units, 2026)

Philips Respironics recalled 113,717 Trilogy Evo ventilators worldwide on March 2, 2026. The recall concerns software Version 1.05.15.00 and the use of non-pneumatic nebulizers with the Trilogy Evo platform. Hospitals and patients should stop using the device immediately and follow recall instructions from Philips Respironics or their healthcare provider.

Philips Respironics
Using non-pneumatic
Read more
Previous
12345...139
Next
Advertisement