These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Shierdu recalled children's wooden building block cactus toys on September 11, 2025. The toys pose a choking hazard, violating the small parts ban. Consumers should stop using them immediately and seek a refund.
E&E Foods recalled 925 cases of Goldband Snapper fillets on September 11, 2025, due to mislabeling. Testing confirmed the product was actually Sharptooth Snapper. Consumers should not eat the fish and should seek a refund.
Blueroot Health recalled Bariatric Fusion Iron Multivitamins on September 11, 2025, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating federal safety standards. Consumers should stop using the product immediately and seek replacement caps.
In My Jammers recalled children's button flare pajama sets due to a burn hazard on September 11, 2025. The pajamas violate mandatory flammability standards, posing a risk of injury to children. Consumers should stop using the pajamas immediately and return them for a full refund.
Epoca International recalled Paris Hilton Mini Beauty Fridges on September 11, 2025. The recall affects about 10,000 units due to fire and burn hazards. Consumers should stop using the product immediately and seek a refund.
Insulet recalled 174,013 units of the Omnipod 5 iOS application on September 11, 2025. A software error can lead to the duplication of numbers during manual entry. This increases the risk of insulin overdelivery, potentially causing hypoglycemia.
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 the BF-H1100 bronchovideoscope on September 11, 2025, due to safety concerns when used with certain medical equipment. The recall affects 1,867 units distributed outside the U.S. Patients and healthcare providers should stop using the device immediately.
Harris Teeter recalled 83 units of Cinnamon Texas Toast on September 11, 2025. The recall occurred due to undeclared milk in the ingredient statement. Consumers in DC, DE, FL, GA, MD, NC, SC, and VA should check their products.
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.
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.
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.
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 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.
Theken Companies recalled 409 Bipolar Hip Implants on September 11, 2025. The devices failed transit testing and may have compromised sterile barriers. Patients and healthcare providers must stop using the implants immediately.
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.
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.