Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
Olympus Corporation of the Americas recalled 4,289 bronchofiberscopes on September 11, 2025. The recall addresses important updates to the instructions for use when combined with specific medical equipment. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled the Bronchovideoscope BF-1TQ170 on September 11, 2025. The recall affects 2,092 units distributed outside the U.S. Additional instructions for safe use with laser and other therapies prompted this action.
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.
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.
CareFusion 303 recalled Alaris Pump Infusion Sets on September 11, 2025, after identifying performance issues. The recall affects multiple model numbers due to potential inaccuracies in flow rate and alarm settings. Healthcare providers must stop using these devices immediately and follow recall 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.
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.
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.
Olympus Corporation recalled 619 bronchoscope units on September 11, 2025. The recall affects the EVIS EXERA b BRONCHOVIDEOSCOPE BF-XT190 due to additional instructions for safe use. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled the Bronchovideoscope BF Type P150 on September 11, 2025. The recall affects 1,019 units distributed outside the U.S. This action follows updates to the instructions for use regarding safe operations with laser and high-frequency therapy equipment.
Olympus Corporation of the Americas recalled 916 units of the EVIS EXERA III Bronchoscope BF-Q190 on September 11, 2025. The recall addresses safety concerns related to its use with laser and high-frequency therapy equipment. Healthcare providers must stop using the device immediately and follow recall instructions.
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.
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.
Olympus Corporation of the Americas recalled 3 bronchovideoscopes on September 11, 2025, due to safety clarification updates. The recall affects 1,987 units distributed outside the US. Healthcare providers must stop using the device immediately to ensure patient safety.
Olympus Corporation of the Americas recalled 1,007 bronchofiberscopes on September 11, 2025, due to safety concerns related to their use with laser and high-frequency therapy equipment. The recall affects devices distributed nationwide in the U.S. and involves additional instructions for safe use.
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 116 units of the BF Type XT40 bronchoscope on September 11, 2025. The recall addresses safety concerns regarding the device's use with laser and high-frequency therapy equipment. Healthcare providers must halt use immediately and follow specific instructions from Olympus.
Boston Scientific recalled the LGX Preconnect with TENACIO Pump on September 11, 2025. The recall affects devices sold in the U.S. and Canada due to inflation and deflation performance issues. Consumers should stop using the device immediately and follow provided instructions.
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.