292 recalls tagged with “toddler product”.
Siemens Medical Solutions USA recalled 182 MAGNETOM Skyra MRI systems worldwide on August 28, 2025. The recall follows a potential ice blockage in the magnet venting system that could cause a helium leak during a quench. Hospitals should stop using affected devices and follow manufacturer instructions for remediation.
B. Braun Medical Inc. recalled 16,228 3000 mL saline irrigation bags nationwide in the United States. The recall cites lack of assurance of sterility due to port misalignment, creating a potential for fluid leakage. Healthcare providers and patients should stop using the product immediately and contact the company for guidance.
B. Braun Medical Inc. recalls 26,316 sterile water bags nationwide after discovery of potential leakage from misaligned ports. The recall covers 3000 mL bags with NDC 0264-7385-60. Health care providers are advised to stop use and contact the company for guidance.
TopCare Health recalled 60 bottles of 70% isopropyl alcohol distributed nationwide by The Kroger Co. The recall cites cross contamination with other products as the hazard. Consumers and healthcare providers should stop using the product immediately and contact the seller for guidance.
Ford recalls 2025 Explorer and Aviator vehicles sold through Ford dealers due to a faulty body control module that can prevent trailer tail lights from illuminating. The defect may reduce visibility for other drivers when towing a trailer. Interim letters alert owners starting Oct 13, 2025, with a final remedy anticipated in April 2026. Ford will perform the repairs at no charge and provide the an
CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.
Frontier Devices recalled 3,790 units of the 12 mm Distraction Pin, REF 301.912S1, distributed nationwide in the United States. The recall cites labeling that includes shelf life which has not been validated. The high-risk device category reflects potential documentation and shelf-life concerns. Healthcare providers and patients should follow recall instructions and contact the manufacturer for a回
Frontier Devices recalled the 301.914S2 14 mm Distraction Pin distributed nationwide in the US. The recall was issued for labeling that includes shelf life not validated. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Frontier Devices and Folsom Metal Products issued a high-risk recall for 490 units of the 16 mm Distraction Pin, REF 301.916S1, distributed nationwide in the United States. The labeling includes shelf life that has not been validated. Patients and healthcare providers should stop using the device immediately and follow recall instructions.
Abbott Point Of Care recalled 9,067,050 i-STAT CG4+ cartridges sold nationwide in the United States. The recall cites a lack of 510(k) premarket clearance to reflect updated sample type for lactate and measurement ranges for pH and PO2. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Itacate Foods LLC recalls 566 packages of CHARGE-UP CHILAQUILES distributed to multiple U.S. states for undeclared Yellow #5 and Yellow #6 color additives. The recall is active as of September 24, 2025. No injuries are reported in the recall notice.
Boston Scientific recalled 28,911 pacemakers worldwide due to a software flaw in Safety Architecture that could prevent Safety Mode when battery impedance is high. The recall covers ACCOLADE family devices and VISIONIST and VALITUDE CRT-Ps. Patients should stop using the device immediately and follow the recall letter instructions.
Boston Scientific recalled 1,380 pacemakers worldwide on August 20, 2025, due to software intended to enhance Safety Architecture. The devices include ACCOLADE family models and VISIONIST and VALITUDE CRT-Ps. The defect could prevent initiation of Safety Mode in ambulatory settings. Patients should stop using the devices and follow manufacturer instructions.
Boston Scientific recalled 190,088 pacemakers worldwide, including ACCOLADE family devices and related CRT-Ps. The software to enhance Safety Architecture could prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state. Patients and healthcare providers should stop using these devices immediately and await manufacturer instructions by letter.
Boston Scientific recalled 3,146 pacemakers worldwide after identifying a software defect that could prevent Safety Mode initiation in an ambulatory setting. Devices include ACCOLADE family models and VISIONIST and VALITUDE CRT-Ps. Patients should stop using affected devices and follow manufacturer instructions.
Boston Scientific is recalling 3,592 pacemakers sold worldwide through hospitals and clinics in 2025. A software feature intended to enhance Safety Architecture may fail to initiate Safety Mode in ambulatory settings due to high battery impedance. Patients and healthcare providers should stop using these devices immediately and follow the recall instructions.
Boston Scientific recalls 3,620 pacemakers worldwide including VALITUDE CRT-P EL and ACCOLADE family devices. A software update is intended to prevent initiation of Safety Mode due to high battery impedance. Patients and clinicians should stop using affected devices and await manufacturer instructions.
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
Aesculap AG recalls the ELAN 4 Fixed Duraguard Long device, Model GB943R, after mislabeling errors were discovered. The U.S. distribution reached Missouri with international distribution to multiple countries. Healthcare providers should stop using the device immediately per manufacturer instructions.
Tampa Maid Foods recalled 776 cases of Panko Style Breaded Butterfly Shrimp due to potential Cesium-137 contamination. The product was distributed to 16 states. Consumers should not eat the shrimp and should contact the company for refunds or replacements.