Arizona recalls

Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.

Due to battery component overheating while charging resulting in melting of internal components and causing smoke.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.

Uneviscerated Fish

Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.

Product Contamination

Unreported Allergens

The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.

The display or "parent" unit of the Max View baby monitors can overheat and/or spark when charging, posing a fire hazard to consumers.

The window opening control devices can break or detach after accidental or other impact, allowing the window to be opened, posing fall and serious injury hazards.

The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system and positional stability requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

The recalled children's toys violate the small parts ban because the small mirror can detach from the toy, posing a deadly choking hazard. In addition, the toys violate the mandatory standard for toys because the toy's mirror has sharp edges, posing a laceration hazard.

The recalled children's chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.