2,715 recalls tagged with “immediate action”.
Abbott recalled 1,958 TactiFlex Sensor Enabled Ablation Catheters on September 10, 2025. The recall follows reports of tip detachment during removal from packaging. Patients and healthcare providers must stop using the device immediately.
Gina Marie Bakery recalled 172 cases of Italian Mixed Vanilla Cookies due to undeclared allergens. The recall affects cookies with undeclared almonds, sesame, and artificial colors. Consumers should stop using the product and seek refunds immediately.
Gina Marie Bakery recalled 172 cases of Toasted Cherry Biscotti on September 10, 2025. The product contains undeclared Red 40, posing a potential health risk. Consumers should not consume the product and are advised to seek a refund or replacement.
Abbott recalled 399 TactiFlex Sensor Enabled Ablation Catheters on September 10, 2025. The recall stems from a limited number of incidents where catheter tips detached during removal from packaging. Patients and healthcare providers must stop using the device immediately and follow recall instructions.
Gina Marie Bakery recalled 172 cases of Italian Sesame Cookies on September 10, 2025. The recall was initiated due to undeclared sesame and artificial colors. Consumers should not consume these cookies and can seek a refund.
Abbott recalled 3,403 TactiFlex Sensor Enabled Ablation Catheters due to potential tip detachment during removal. The recall affects medical devices distributed worldwide. Patients and healthcare providers must stop using the device immediately.
Gina Marie Bakery recalled 172 cases of Vanilla Cookies with Raspberry Peach Jam due to undeclared Red 3 and Blue 1. The recall was initiated on September 10, 2025, after notification to the FDA. Consumers should not consume the product and seek refunds.
Gina Marie Bakery recalled 172 cases of Toasted Almond & Cherry Biscotti on September 10, 2025. The recall stems from an undeclared allergen, Red 40. Consumers should not eat the product and seek refunds.
Biomet recalled 40 units of Juggerknot Mini Soft Anchors on September 9, 2025. The recall stems from a labeling error where the carton contains 1.4mm Short devices instead of the labeled 1.0mm Mini products. Patients and healthcare providers must stop using these devices immediately.
BioPro recalled 147 femoral head components on September 9, 2025. A packaging defect may compromise sterility, increasing infection risk. The recall affects models distributed in Texas and Michigan.
Whole Foods Market recalled Blueberry Almond Granola on September 9, 2025. The product contains undeclared allergens including wheat, sesame, and cashew. Six units, packaged in one-pound containers, were sold at one store in Philadelphia, PA.
BioPro recalled 147 units of Endo Heads on September 9, 2025. A packaging issue may compromise the sterile barrier, leading to infection risk. Healthcare providers and patients should stop using the devices immediately.
Draeger recalled 530 Atlan A350 anesthesia workstations due to potential ventilation failures. The recall occurred on September 9, 2025, after reports of critical device malfunctions during use. Patients and healthcare providers must stop using the device immediately.
MedicalCommunications GmbH recalled 474 units of HEYEX PACS software on September 9, 2025. The software may inaccurately report measured values, posing risks to patient care. Users should stop using the software immediately and follow recall instructions.
Hale recalled 54 bottles of Roasted Garlic Infused Olive Oil on September 9, 2025. The product may be contaminated with Clostridium botulinum and was manufactured without an approved process. Consumers should stop using the product immediately and seek a refund or replacement.
Lotsa Pasta International Food Shop recalled 54 bottles of Fresh Basil Infused Olive Oil on September 9, 2025. The product may be contaminated with Clostridium botulinum due to improper manufacturing processes. Consumers should not consume the product and seek a refund or replacement.
BioPro recalled 147 bipolar heads on September 9, 2025, due to a potential packaging issue. The defect may compromise the sterile barrier, increasing infection risks if implanted. Healthcare providers and patients should stop using these devices immediately.
Eureka recalled 32 cases of cinnamon on September 9, 2025, due to elevated lead levels. Consumers should not consume the product and seek refunds. The recall affects retail and wholesale customers in California and Michigan.
Draeger recalled 223 Atlan A350XL anesthesia workstations on September 9, 2025. The devices may fail during mechanical ventilation, posing serious health risks. The recall affects states across the U.S. and several countries worldwide.
NOXBOX recalled 1,667 Nitric Oxide Delivery Systems on September 9, 2025. The recall stems from dangerous dose fluctuations that could occur under specific device settings. Healthcare providers and patients should stop using the device immediately.