1,862 recalls tagged with “stop use immediately”.
Encore Medical, LP recalled 14 EMPOWR 3D Knee implants on January 15, 2026. The implants contain incorrect labeling that poses a risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.
Rose and Shore recalled 5,067.1 cases of 14" Margarita Thin Crust Pizza sold at a single regional chain in California, Oregon, Arizona, Idaho and Texas. A potential foreign object has been found in tomatoes used in the product. Consumers should not eat this pizza and should contact Rose and Shore for refund or replacement by email.
Sevillo Fine Foods recalled 520 units of Slow Roasted Diced Tomatoes distributed to California and North Carolina after the product may contain metal fragments. The product is frozen and packaged in bulk with a plastic liner inside a cardboard box. Consumers should not eat the product and should contact Sevillo Fine Foods for refund or replacement via email.
Sevillo Fine Foods recalled 2,372 units of Slow Roasted Diced Tomatoes distributed to California and North Carolina. The product may contain metal fragments. Consumers should not consume the product and should contact Sevillo Fine Foods for refunds or replacements.
KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.
Edermy LLC recalled 11,202 medical devices on January 14, 2026. The recall affects models P2HC-A, P2HC-S, and P2HC due to lack of proper FDA clearance. Patients and healthcare providers should immediately cease use of these devices and follow recall instructions.
Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.
Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.
Medtronic recalled two units of the Octopus Nuvo Tissue Stabilizer on January 13, 2026, after identifying an assembly issue. The tubing was incorrectly positioned, posing a high hazard risk to patients. Healthcare providers and patients must stop using the device immediately to prevent potential complications.
Diva Fam Inc recalled approximately 5.4 million units of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume the product and should seek refunds or replacements.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The recall follows potential contamination with Clostridium botulinum, a dangerous toxin. Consumers should not consume the product and seek refunds or replacements immediately.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume the product and seek refunds immediately.
Diva Fam Inc recalled approximately 5.4 million jars of Sea Moss Gel on January 9, 2026, due to potential Clostridium botulinum contamination. Consumers should not consume the product and are advised to seek refunds. The recall affects multiple lot codes sold nationwide.
FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.
Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.
Volkswagen Group of America recalled certain 2025 Tiguan vehicles due to a loose tie rod bolt. This condition may lead to a loss of vehicle control, increasing crash risk. Owner notification letters were mailed on September 5, 2025.
Kalencom Corporation recalled SARO Braided Crib Bumpers on January 8, 2026, due to suffocation risks. The bumpers can obstruct an infant's breathing, violating federal safety regulations. Consumers should stop using the product immediately and seek a refund.
Vasicar recalled 18,000 dressers on January 8, 2026, due to tip-over risks. The dressers can cause serious injury or death if not anchored to the wall. Consumers should stop using them immediately and seek a refund.
Isla Rae recalled magnetic wireless chargers on January 8, 2026, due to risks of fire and burn hazards. Consumers should stop using the chargers immediately and seek refunds. The chargers were sold at T.J. Maxx and Marshalls locations between June 2024 and November 2025.
Marcus Adler Glove recalled Julie and Judah pajama pants and shorts on January 8, 2026. The products violate mandatory flammability standards for children's sleepwear. Consumers should immediately stop using these items and seek a refund.