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.
1,488 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
AVID Medical recalled 228 units of the Halyard CPT BASIC IR Pack on August 4, 2025. The recall follows reports of open header bag seals that may compromise sterility. Healthcare providers and patients should stop using the 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.
Hans Kissle Company recalled 66 units of Red Bliss Potato Salad on August 4, 2025, due to undeclared wheat. The product is mislabeled as potato salad but contains pasta salad. Consumers should not eat the product and should seek a refund or replacement.
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.
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.
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.
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.
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.
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.
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 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 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.
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 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.
Exela Pharma Sciences recalled 4.2% Sodium Bicarbonate Injection on July 30, 2025, due to arsenic contamination. The recall affects single-dose vials distributed nationwide. Consumers and healthcare providers must stop using the product immediately.
Contract Medical International GmbH recalled 2,500 Fortress Introducer Sheath Systems on July 30, 2025. Units may have incorrect pouch labeling, leading to potential use of the wrong device version. Patients and healthcare providers should stop using the product immediately.
S.I.N. Implant System Ltda recalled 4,367 dental implants on July 30, 2025, due to improper storage conditions. The recalled products may have compromised packaging, affecting their quality and performance. Patients and healthcare providers should stop using these devices immediately.
Pfizer Inc. recalled 29,004 bottles of Levoxyl on July 29, 2025, due to subpotency. The recall affects levothyroxine sodium tablets, 50 mcg, Rx only, distributed in the U.S. Consumers should stop using the product immediately.