Browse through 1,540 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
B. Braun Medical Inc. recalled 74,088 containers of Lactated Ringer's Injection on August 4, 2025. The recall stems from a lack of assurance of sterility and potential fluid leakage. Consumers and healthcare providers should discontinue use immediately and seek guidance.
AVID Medical recalled 57 units of the Halyard ENT Pack on August 4, 2025. The recall stems from potential open header bag seals that may compromise sterility. Patients and healthcare providers must stop using this device immediately.
Wasatch Photonics recalled 192 Raman spectrometers on August 4, 2025. Two potential laser safety failure modes could pose serious risks. No incidents have been reported, but excessive force or vibration may trigger failures.
Hospira, Inc. recalled 49,620 vials of Epinephrine Injection on August 4, 2025. The recall follows concerns about the lack of assurance of sterility. Consumers should stop using the product immediately.
Beckman Coulter recalled 116 DxC 500i Clinical Analyzer modules on August 4, 2025, due to potential processing delays. The defect may impact the accuracy of test results when ordering certain tests simultaneously. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
DFA Dairy Brands recalled 54 cases of Friendly's Ice Cream on August 1, 2025. The product contains undeclared wheat and soy, posing a serious allergen risk. Consumers in Maryland, Virginia, and Pennsylvania should not consume the affected ice cream.
Backyard Kids recalled KidKraft Farm to Table play kitchens on July 31, 2025, after a strangulation hazard was identified. One death has been reported linked to the defect. The recall affects units designed for children ages 3 and older, model number 53411.
Tegu recalled its Magnetic Floating Stackers on July 31, 2025, after discovering a magnet ingestion hazard. The recall affects model numbers STA-BGY-801T and STA-BTP-806T. The toys can pose serious injuries or death if magnets detach and are swallowed.
TTI Consumer Power Tools recalled RIDGID 18Volt Brushless Framing Nailers on July 31, 2025. The recall affects approximately 50,000 units due to a malfunctioning trigger mechanism that poses a laceration hazard. Consumers should stop using these nailers immediately and check for eligibility in the recall.
Baby Loren recalled children's loungewear on July 31, 2025, due to serious burn risks. The loungewear violates federal flammability standards, endangering children. Affected items include dresses in various prints and sizes 2T to 6Y.
Amazon recalled Amazon Basics Premium Foam Eurotop Mattresses on July 31, 2025, due to fire hazards. The mattresses violate federal flammability standards, posing serious risk to consumers. Affected models were sold on Amazon from December 2022 through May 2024.
Leatherman recalled Charge Plus and Charge Plus TTi multi-tools on July 31, 2025, due to a laceration hazard. The knife blade tip does not fully fold into the handle, posing a risk of injury. Consumers should stop using the tools immediately and check for recall eligibility.
Dorel Home Furnishings recalled Cosco 2-step kitchen steppers on July 31, 2025. The safety bar can detach, posing fall risks. Consumers should stop using the product and seek repairs immediately.
Waldemar Link GmbH & Co. KG recalled eight units of the LinkSymphoKnee Tibial Component on July 31, 2025. The recall stems from a manufacturing error involving uncoated security screws. Patients and healthcare providers should stop using the device immediately.
IKEA recalled garlic presses on July 31, 2025, after reports of small metal pieces detaching. The recall affects the IKEA 365+ VÄRDEFULL models with the IKEA logo. Consumers should stop using these products immediately and return them for a refund.
Medline Industries recalled 7,913 reprocessed electrophysiology catheters on July 31, 2025. Residual particulates on patient-contacting surfaces pose a risk of serious infection and thrombus formation. Patients and healthcare providers must stop using these devices immediately.
Medline Industries recalled 7,913 reprocessed AcuNav Ultrasound Catheters on July 31, 2025. The devices may contain harmful residual particulates that pose an infection risk. Patients and healthcare providers should stop using these devices immediately and follow recall instructions.
Medline Industries recalled 7,913 electrophysiology catheters on July 31, 2025, due to contamination concerns. Specific lots may contain small residual particulates, posing risks of systemic infection and thrombus formation. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 7,913 reprocessed ViewFlex Xtra ICE catheters on July 31, 2025. The recall affects specific lots due to potential residual particulates that may cause serious health risks. Patients and healthcare providers must stop using the devices immediately.
Medline Industries recalled 7,913 reprocessed electrophysiology catheters on July 31, 2025. The recall affects specific lots that may contain harmful particulates. Using these catheters could lead to serious health risks including embolism or deep vein thrombosis.