527 recalls tagged with “adult product”.
B Braun Medical recalled approximately 259,392 IV Administration Sets on October 29, 2025, due to a risk of medication backflow. The recall affects products with catalog number 490309 distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore.
B Braun Medical recalled 41,976 IV administration sets on October 29, 2025. The recall stems from a risk of medication backflow into primary IV containers. Affected products include catalog number 490354, distributed worldwide.
B Braun Medical issued a recall for 1,250 IV administration sets on October 29, 2025. The recall stems from a potential backflow of medication between IV containers, posing a serious risk to patients. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical recalled 286,400 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary IV containers. Users must stop using the devices immediately and follow the manufacturer's instructions.
B Braun Medical recalled 111,312 IV administration sets due to a risk of backflow of medication. The sets are used with Infusomat Space, Outlook, and Vista Basic Pump models. The recall was announced on October 29, 2025, following potential safety issues.
B Braun Medical recalled 960 IV administration sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista pumps. Users face a high risk of medication backflow and occlusion.
B Braun Medical recalled 19,104 IV administration sets on October 29, 2025. The recall stems from a potential for medication backflow and inability to prime. The affected sets were distributed worldwide, including the US and Canada.
B Braun Medical recalled 4,536 IV administration sets on October 29, 2025. The recall affects devices that may allow backflow of medication from secondary IV containers. This poses a high risk to patients using the Infusomat Space, Outlook, and Vista Basic pumps.
B Braun Medical recalled 129,480 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary containers. Patients and healthcare providers must stop using the devices immediately.
B Braun Medical recalled 23,160 IV administration sets on October 29, 2025. The sets pose a high risk of medication backflow from secondary containers into primary containers. Healthcare providers should stop using the devices immediately.
B Braun Medical recalled 32,436 Anesthesia IV Sets on October 29, 2025. The recall affects specific catalog numbers due to a risk of medication backflow. Healthcare providers must stop using these devices immediately and follow the provided recall instructions.
B Braun Medical recalled 104,784 Anesthesia IV Sets on October 29, 2025. The recall affects models utilized with Infusomat Space, Outlook, and Vista pumps due to potential medication backflow. This hazard poses serious risks for patients receiving IV medication.
Siluetaya recalled 40 bottles of SiluetaYa Mexican Tejocote Roots Supplement Pieces sold online to consumers in AZ, CA, NM, NY, TX, and UT. The product contains yellow oleander. Consumers should not consume this product and contact Siluetaya, LLC for refund or replacement.
Agebox recalled its iKids-Growth Night Formula due to the presence of undeclared ibutamoren. The recall affects 60-count bottles manufactured exclusively for AGEBOX Inc. Consumers should stop using the product immediately and contact Agebox or their healthcare provider for guidance.
AGEBOX Inc. recalled 665 bottles of iKids-Growth capsules on October 28, 2025, due to undeclared ibutamoren. The product was marketed without an approved NDA/ANDA. Consumers should stop using the product immediately and contact Agebox for guidance.
Medline Industries recalled 182,526 units of CURAD Germ-Shield Touch-Free Fabric Bandages due to compromised sterility. The recall affects all lots manufactured and distributed in the US, Guam, Canada, and the UAE. Consumers must stop using these bandages immediately.
Medline Industries recalled 1.57 million units of Curad Touch-Free and Quick-Strip Bandages on October 27, 2025. The packaging may exhibit open seals, compromising sterility. Consumers should stop use immediately and follow the recall instructions provided by the manufacturer.
Cipla USA recalled 1,180 boxes of Lanthanum Carbonate chewable tablets on October 24, 2025. The recall follows a failure to meet stability specifications for hardness tests. Consumers and healthcare providers must stop using the product immediately.
Water Pure recalled 17,612 bottles of My Bladder dietary supplement on October 24, 2025. The product may be contaminated with E. coli O7:K1 and E. coli 1303. Consumers should stop use immediately and seek refunds.
MeriCal, LLC recalled 698,064 units of its Super Greens Dietary Supplement on October 24, 2025. The recall follows potential contamination with Salmonella Richmond. Consumers should not consume the product and seek refunds immediately.