2,228 recalls tagged with “stop use 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.
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.
Medline Industries recalled 150 dialysis convenience kits on January 8, 2026, due to silicone seal defects. Affected kits may obstruct fluid paths and risk exposure to biological contaminants.
Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.
Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.
Medline Industries recalled 31,848 dialysis dressing change kits on January 8, 2026. The recall follows reports of defective silicone seals on Tego Connectors that may occlude fluid paths. This defect can delay therapy and expose patients to biological contaminants.
Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.
Olympus Corporation recalled 4,183 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. Devices may deform and lose performance due to inadequate thermoforming. Healthcare providers should immediately stop using the affected products and follow recall instructions.
Olympus Corporation of the Americas recalled 93 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to a manufacturing flaw. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 5,946 single use sphincterotomes on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must cease use immediately to avoid potential hazards.
Olympus Corporation recalled 1,474 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must stop using these instruments immediately.
Olympus Corporation of the Americas recalled 10,008 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to a manufacturing issue. Healthcare providers and patients must stop using them immediately.
Olympus Corporation of the Americas recalled 136,037 Single Use 3-Lumen Sphincterotome V devices on January 7, 2026. The recall affects devices that did not undergo proper thermoforming, risking deformation and loss of performance. Healthcare providers and patients must stop using the devices immediately.
Olympus Corporation of the Americas recalled 30,489 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The recall stems from devices that failed to undergo proper thermoforming, risking deformation and performance loss. Healthcare providers and patients must stop using the device immediately.