1,817 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Advanced Pharmaceutical Technology recalled 22,843 cartons of TESTO-100 CIII testosterone pellets on October 3, 2025. The recall follows a risk of microbial contamination that could compromise product sterility. Consumers and healthcare providers should stop using the product immediately and seek guidance.
Almpal recalls its dissolved oxygen test kits sold on Amazon after authorities found the sulfuric acid inside the kit lacked required child-resistant packaging. The recall is active as of Oct 2, 2025. Consumers should stop using the kit and follow disposal and refund instructions from the seller.
ICU Medical recalls 23,203 IV gravity burette sets worldwide. The burette component is missing an internal shutoff valve, which can delay therapy, cause overdelivery, or allow air to be infused. Stop using the device and contact ICU Medical for instructions.
Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.
Church & Dwight recalled 21,912 bottles of ZICAM Cold Remedy Medicated Fruit Drops Elderberry from nationwide distribution in the United States. The label did not indicate elderberry as an ingredient though the product contains elderberry. Consumers should stop using the product and contact Church & Dwight for guidance.
Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.
SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.
B BRAUN MEDICAL recalled 1,298,454 STREAMLINE BLOODLINE SET FOR DIALOG devices nationwide in the United States after observations of micro-air bubbles and air-in-line alarms linked to damaged arterial and venous connectors. The defect increases the risk of air entering the bloodstream during dialysis. Patients and healthcare providers should stop using this device immediately and follow the recall
Acella Pharmaceuticals recalls doxycycline hyclate tablets, 100 mg, 500-count bottles distributed nationwide in the USA. Stability testing found the lot did not meet dissolution specifications. Consumers and healthcare providers should stop using the product immediately and contact Acella for guidance.
AFCO's hand sanitizer 5515 is being recalled nationwide through distributors and retailers. The recall cites cGMP deviations that left methanol risk unexcluded. Consumers and healthcare providers should stop using this product immediately and contact Acuity Specialty Products for guidance.
Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.
Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.
Dr. Reddy's Laboratories Inc. recalled 571 vials of Succinylcholine Chloride Injection, USP nationwide in the United States. The recall cites an out-of-specification result during six-month stability testing due to decreased preservative concentration. Healthcare providers and patients should stop using the product immediately and await guidance from the recall letter.
Synthes (USA) Products LLC recalled 120 low-profile locking screws for intramedullary nails used in the RFN-Advanced Retrograde Femoral Nailing System and the Tibial Nail Advanced System. The recall covers devices distributed worldwide through healthcare providers. The external packaging mislabels screw lengths: 42 mm screws are labeled 46 mm and 46 mm screws are labeled 42 mm. Hospitals and spine
Synthes USA recalled 122 locking intramedullary nail screws used in RFN-Advanced and Tibial Nail Advanced systems. The recall covers worldwide distribution including the US and Canada. The packaging labeling misstates screw length while the etched length on the screw is correct. Healthcare providers should stop using the device immediately and follow recall instructions from Synthes.
Mad Rabbit recalls RELIEVE lidocaine numbing cream due to non‑compliant packaging that could allow poisoning of young children. The recall covers a product sold under the Mad Rabbit brand and issued on 2025-09-25. The packaging does not meet the Poison Prevention Packaging Act requirement for child resistance. Consumers should stop using the product immediately and contact Mad Rabbit for a free, a
DJO recalled 1,594 Cold Form Wraps for back and shoulder use nationwide through multiple retailers. The IFU directs heating in a microwave for 3 minutes, which can cause leaks or seam breaks and temperatures high enough to cause a second-degree burn. Stop using the device and follow the manufacturer’s recall instructions.
LeMaitre Vascular recalled 1 Artegraft AG1015 vascular graft distributed to Arkansas hospitals after a packaging size labeling error. The packaging error could lead to using the wrong size graft during surgery. Hospitals and patients should stop using the device and follow recall instructions. See the recall letter for instructions from LeMaitre Vascular or your healthcare provider.
Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.
Ent ecavir 0.5 mg tablets, distributed nationwide in the United States by Zydus Pharmaceuticals USA Inc., are recalled, affecting 912 bottles. The recall is due to an out-of-specification organic impurity detected in a batch, Class II. Healthcare providers and patients should stop using the product immediately and contact Zydus Pharmaceuticals USA for guidance.
Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.
BD recalled 177 units of the BACTEC Blood Culture System worldwide after an unauthorized actor accessed product service credentials. The breach could allow unauthorized access to system configurations and data. Healthcare facilities should stop using the affected equipment and follow BD’s recall instructions.
BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.
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