Ohio recalls

Asclemed USA Inc. is recalling Lidocaine HCl Injection USP 1% in 5 mL single-dose ampules due to lack of assurance of sterility. The affected lots were distributed nationwide. This is a precautionary measure to prevent potential infection risk from non-sterile product.

Asclemed USA Inc. is recalling specific lots of Accucaine, a lidocaine injection used for local anesthesia, because the manufacturer cannot guarantee the product is sterile. This affects multiple lot numbers distributed nationwide.

Boehringer Ingelheim Pharmaceuticals is recalling one lot of Synjardy XR 12.5/1000 mg tablets due to manufacturing quality control issues. During production, an incorrect cleaning agent was used on equipment, and required testing of that equipment was not completed before the tablets were made.

Accord Healthcare is recalling one lot of levothyroxine sodium 300 mcg tablets because they may contain less active ingredient than labeled. This means the medication may not work as intended for patients who need it to manage thyroid conditions.

Lupin Pharmaceuticals is recalling multiple lots of prednisolone acetate ophthalmic suspension 1% (an anti-inflammatory eye drop) due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.

Accord BioPharma is recalling one lot of IMULDOSA (ustekinumab-srlf) injection due to lack of assurance that the product is sterile. The affected lot may not meet sterility standards required for injectable medications. No injuries have been reported.

BD ChloraPrep CLear applicators intended for further processing and sterilization were distributed directly to customers without being sterilized first. The product is a skin antiseptic used before medical procedures. No injuries have been reported.

BD ChloraPrep CLear, a chlorhexidine-based skin antiseptic solution in single-use applicators, was distributed without proper sterilization. Unsterilized applicators intended for further processing were mistakenly sent to customers outside the intended distribution channel. This affects 18,000 units across multiple lot numbers distributed nationwide.

BD ChloraPrep Scrub Teal applicators intended for further processing and sterilization were mistakenly distributed as finished sterile products. The affected applicators may not meet sterility standards required for safe use in medical settings.

BD ChloraPrep Scrub Teal applicators intended for further processing and sterilization were distributed to customers without having been sterilized. The unsterilized applicators reached customers outside the intended distribution channel. About 1,200 units are affected.

BD ChloraPrep Hi-Lite Orange skin antiseptic applicators were distributed without proper sterilization. These units were intended for further processing and sterilization before use, but were instead sent directly to customers. This creates a risk of infection if the applicators are used as distributed.

BD ChloraPrep Hi-Lite Orange applicators intended for further sterilization before use were mistakenly distributed directly to customers without undergoing the required sterilization process. These applicators are used to prepare skin before medical procedures and must be sterile to be safe. The recall affects specific lot numbers distributed nationwide.

CareFusion distributed unsterilized ChloraPrep FREPP applicators (chlorhexidine gluconate and isopropyl alcohol solution) to customers outside their intended distribution channel. These applicators were meant for further processing and sterilization before use, but were shipped to end users without that sterilization step, creating a risk of infection if used on patients.

BD ChloraPrep Clear applicators (a skin-prep solution containing chlorhexidine and isopropyl alcohol) were distributed without proper sterilization. These applicators were intended to be sterilized before sale but were sent to customers in an unsterilized state. The affected products are in 3 ml applicator packs, with multiple lot numbers expiring between June 2026 and February 2029.

BD PurPrep sterile applicators (povidone-iodine with isopropyl alcohol) were distributed without proper sterilization assurance. Unsterilized applicators intended for further processing were shipped to customers outside the intended distribution channel, affecting Lot 4298581 (expires 09/30/2026).

BD ChloraPrep Hi-Lite Orange applicators (a skin antiseptic used before medical procedures) were distributed without proper sterilization. These applicators were intended to be sterilized before use, but some unsterilized units were sent to customers outside the normal supply chain.

Lupin Pharmaceuticals is recalling certain lots of its Glucagon Emergency Kit because the syringe plunger may not move smoothly during use. This defect was discovered during stability testing and could prevent the kit from working properly in an emergency.

Mars Petcare discovered that two lots of Pedigree High Protein Chopped Chicken & Duck Flavor wet dog food were fraudulently diverted into stores after being sent for destruction due to quality concerns. The affected cans may contain pieces of sharp metal and plastic that could harm dogs if eaten.

Winco Fireworks International is recalling Roman Candles 8 Shot fireworks (Model RCLR-W8012) because they can malfunction. During use, shots may blow out the side of the tube instead of firing normally, creating a risk of serious injury from explosions and burns.

Winco Fireworks International is recalling Unity 7 Shot 200 Gram Aerial Cake fireworks (model MEF6096) because they can tip over during use, creating a risk of serious injury from explosion and burns. The affected fireworks were sold in red, white and blue packaging at Pyro City and independent fireworks retailers nationwide between January and May 2026.

Small metal wire bristles can detach from Cuisinart grill brushes during use and stick to food or the grill. If swallowed, these bristles can cause serious internal injuries requiring surgery. Conair has received 54 reports of detached bristles, including 3 cases where consumers needed medical treatment to remove bristles from their throat or digestive tract.

Junpower CR2032 lithium coin batteries sold on Amazon lack the child-resistant packaging and warning labels required by federal law. If swallowed, these batteries can cause serious internal injuries or death. About 67,000 units were sold between December 2023 and September 2024.

The LED board inside Metalux Optimized High Bay light fixtures can overheat or contact the lens and nearby combustible materials, creating a fire hazard. The company has received nine reports of these fixtures catching fire. About 42,000 fixtures sold since April 2020 are affected.

The clear plastic dome on this toy can detach from the base, exposing small plastic balls inside that children can choke on. Target has received nine reports of the dome detaching, including one incident where a child began to choke.

AMASKY nursing pillows sold on Amazon can obstruct an infant's breathing during feeding or tummy time. The pillows do not meet federal safety standards for nursing pillows and infant support cushions. About 4,000 pillows are affected.

The lithium-ion battery in certain Rowenta X-Force Flex cordless vacuum cleaners can overheat and ignite, creating a risk of fire and burn injuries. The recall affects two models sold between July 2023 and January 2026.

These LED finger light toys contain button cell batteries that children can easily access and swallow. Swallowing button cell batteries can cause serious internal injuries, including chemical burns, and can be fatal.

CVS Health Medicated Hemorrhoidal Wipes contain lidocaine and are required to have child-resistant packaging by federal law, but this product does not. Young children could open the wipes and ingest the contents, causing serious injury or death. No injuries have been reported.

Topyond pool drain ports with covers do not meet federal safety standards and pose a risk of entrapment and drowning. The plastic drain ports (model SP-2850V) were sold online starting in May 2024 and do not provide adequate protection against the hazards they are designed to prevent.

Vevor baby loungers have sides that are too low to safely contain an infant and openings at the foot that are wider than safety standards allow. The loungers also lack a stand, creating a fall hazard if placed on elevated surfaces. These defects violate mandatory infant sleep product safety standards and can cause serious injury or death.