2,715 recalls tagged with “immediate action”.
Boston Scientific recalled the TENACIO Pump on September 11, 2025. The device may exhibit inflation and deflation performance issues. Patients must stop using the pump immediately and follow the manufacturer's instructions.
Olympus Corporation of the Americas recalled the Bronchofiberscope Model No. BF-TE2 on September 11, 2025. The recall affects 5,287 units due to safety concerns when used with laser and high-frequency therapy equipment. Users should stop using the device immediately and contact Olympus for further instructions.
Olympus Corporation of the Americas recalled the BF-1TH1100 bronchoscope on September 11, 2025. The recall addresses safety concerns regarding the use of the device with certain laser therapy equipment. Healthcare providers and patients must stop using this device immediately to ensure safety.
Olympus Corporation of the Americas recalled 395 units of the EVIS EXERA II Bronchovideoscope BF Type Q180-AC on September 11, 2025. The recall addresses additional instructions for safe use with laser and high-frequency therapy equipment. Healthcare providers must stop using the device immediately.
Olympus Corporation recalled 4,297 EVIS EXERA III bronchoscopes on September 11, 2025. The recall follows updates to the instructions for use regarding safe operation with laser and high-frequency therapy equipment. Healthcare providers and patients must stop using the device immediately.
Harris Teeter recalled 295 units of Asiago Texas Toast on September 11, 2025. The recall stems from undeclared milk allergens not listed on the packaging. Consumers should avoid the product and seek a refund or replacement.
Ferno-Washington Inc recalled 138 powered ambulance cots on September 11, 2025. The fastening post hardware may loosen, posing a risk of detachment during use. Users should stop using the product immediately and follow the recall instructions.
Ethicon Endo-Surgery recalled three units of the ECHELON LINEAR Cutters Reload 80 mm Blue on September 11, 2025. The devices were shipped unsterilized, posing a high health risk. The recall affects surgical devices in the United Arab Emirates.
Tropicana Brands Group recalled 1,599 cases of apple juice on September 11, 2025. A manufacturing deviation may cause spoilage or microbial contamination. The affected juice was distributed in 12 states, including Texas and Colorado.
Boston Scientific recalled 172 units of its CXR Preconnect with TENACIO Pump on September 11, 2025. The recall stems from potential inflation and deflation performance issues. The devices were distributed worldwide, including the US and Canada.
Boston Scientific recalled 59 units of the TENACIO Pump with InhibiZone on September 11, 2025. The recall addresses potential inflation and deflation performance issues. Patients should stop using the device immediately and follow the manufacturer's instructions.
Olympus Corporation of the Americas recalled 1,473 EVIS EXERA II Bronchoscopes on September 11, 2025. The recall addresses critical updates to the instructions for use when combined with laser and coagulation therapies. Healthcare professionals must stop using the device immediately and follow the manufacturer's instructions.
Olympus Corporation of the Americas recalled 3,216 bronchoscope units on September 11, 2025. The recall affects 347 units in the U.S. and includes critical updates to instructions for use. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled 3,046 units of its EVIS EXERA III bronchoscope BF-P190 on September 11, 2025. The recall addresses safety concerns regarding the use of the bronchoscope with laser and high-frequency therapy equipment. Healthcare providers must stop using this device immediately.
Medline Industries recalled 8,267,150 saline flush syringes on September 11, 2025. The syringes may not meet the required concentration of sodium chloride. Consumers and healthcare providers must stop using these products immediately.
Olympus Corporation of the Americas recalled 5,221 units of the EVIS EXERA III Bronchoscope BF-H190 on September 11, 2025. The recall aims to address safety concerns when used with laser and high-frequency therapy equipment. Healthcare providers and patients 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 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.
Goot Essa recalled 62 pounds of Der Mutterschaf Cheese on September 10, 2025. A positive Listeria Monocytogenes test prompted the recall. The affected cheese was distributed in Connecticut, New Jersey, Montana, and Virginia.
Gina Marie Bakery recalled 172 cases of Vanilla with Apricot Jam Cookies on September 10, 2025. The recall follows the discovery of undeclared Red 40 and Yellow 6 in the product. Consumers should not eat these cookies and seek refunds.