Georgia recalls

Moisture can get trapped inside these bath foam containers and build up pressure. When opened, pieces may shoot out forcefully and hit someone. The company has received three reports of injuries, including bruises, swelling, and a chipped tooth.

Somgem Pig and Yomin Toilet Lighters sold on Amazon lack required child-resistant safety features, creating a serious fire and burn hazard. About 11,710 of these novelty lighters were sold between July 2022 and November 2025.

Royal Oak flame saber lighters do not have the required child-resistant safety mechanism, which means children can operate them and cause serious burns or fires. The lighters also lack required safety labels. About 190,560 units were sold nationwide from November 2023 through October 2025.

Dupray Neat Steam Cleaners can rupture if overfilled or if the pressure release valve malfunctions, potentially spraying hot steam and causing burns or serious injuries. The company has received 15 reports of boiler ruptures, including four reports of burns, bruises, lacerations, and a broken wrist.

The metal retaining pins inside some PQL High Bay Linear LED light fixtures can wear down over time, allowing the LED board to come loose. A loose board inside the fixture can overheat and catch fire. One fixture has already caught fire, though no injuries have been reported.

Vevor safety gates have a gap between the gate and the floor that is large enough for a child's torso to fit through, creating a risk of entrapment and serious injury. The gates were sold online between December 2023 and December 2025 in three width sizes.

Stryker is recalling certain MOLLI 2 surgical marker systems because the instructions for use need to be updated. Magnetized surgical tools used during the procedure may dislodge the markers that are placed to mark the surgical site. Stryker is providing updated labeling to address this issue.

Centinel Spine's Prodisc C SK cervical disc replacement devices were labeled as 6mm but actually contained 5mm products. This mislabeling affects 20 units distributed across eight states. The size difference could affect surgical fit and patient outcomes.

Medline Industries identified calibration problems with equipment used to sterilize and package certain surgical packs. While the packs went through the standard sterilization process, the equipment issues may have affected their sterility. This recall affects specific lot numbers of Universal UltraGard and Shoulder Drape Pouch surgical packs.

Medline has recalled multiple models of surgical gowns due to calibration problems with sterilization equipment. While the gowns went through sterilization cycles, equipment calibration issues may have affected their sterility. No injuries have been reported.

Medline Industries recalled multiple surgical drape products due to calibration problems with sterilization equipment. While the drapes went through sterilization and packaging, equipment calibration issues may have compromised their sterility. No injuries have been reported.

Medline discovered that equipment used to sterilize and package certain arthroscopy surgical kits had calibration problems. While the kits went through sterilization, the equipment issues may have affected whether the products met required sterility standards. No injuries have been reported.

Medline has recalled multiple surgical convenience kits used in orthopedic and neurosurgery procedures due to calibration issues with sterilization equipment. While the kits went through sterilization cycles, equipment calibration problems may have affected their sterility assurance. No injuries have been reported.

Medline Industries identified calibration problems with equipment used to sterilize and package certain surgical and eye surgery convenience kits. Although the kits went through sterilization cycles, the calibration issues may have affected how reliably the sterilization worked. No infections or injuries have been reported.

Medline Industries recalled multiple surgical convenience kits used in hospitals and surgical centers because equipment used to sterilize and package them had calibration problems. Although the kits went through sterilization cycles, the calibration issues may have affected their sterility. No injuries have been reported.

Medline Industries recalled multiple surgical convenience kits used in gynecological and other procedures because of calibration problems in the sterilization equipment. Although the kits went through standard sterilization cycles, the equipment issues may have compromised their sterility.

Medline Industries recalled multiple models of C-section surgical convenience kits due to calibration problems with sterilization equipment. While the kits went through sterilization cycles, equipment calibration issues may have compromised their sterility. No injuries have been reported.

Medline Industries identified calibration problems with sterilization equipment used to process certain urology surgical kits. While the products went through sterilization cycles, the equipment issues may have affected whether the devices are truly sterile. This affects five models of urology kits distributed nationwide.

Medline has recalled multiple surgical convenience kits used in gynecological, urological, and other surgical procedures due to calibration problems with sterilization equipment. Although the kits went through sterilization cycles, the equipment calibration issues may have affected their sterility assurance level, potentially compromising the sterility of the devices.

Medline Industries identified calibration problems with equipment used to sterilize and package obstetric and gynecology convenience kits. While the kits went through sterilization cycles, the equipment calibration issues may have affected whether the products met required sterility standards. No injuries have been reported.

Medline recalled multiple neurological surgical kits due to calibration problems in the sterilization equipment used to process them. Although the kits went through the standard sterilization process, calibration issues may have reduced the sterility assurance level of the products.

Medline Industries has recalled certain Chest/Breast-LF Convenience Kits (Model DYNJ83950) because equipment used to sterilize and package them had calibration problems. While the kits went through sterilization cycles, the calibration issues may have affected whether they meet required sterility standards. No injuries have been reported.

Medline identified calibration problems with sterilization equipment used to process certain LVAD driveline and central line dressing change trays. These issues may have affected the sterility of the devices, even though they went through standard sterilization cycles. The recall affects specific lot numbers manufactured between 2020 and 2025.

Medline has recalled certain batches of its Admit Kit (model DYKA1343A) due to calibration problems with the sterilization equipment used to package them. While the kits went through sterilization, the equipment issues may have affected how well they stayed sterile. No injuries have been reported.

Medline identified calibration problems with equipment used to sterilize and package two models of convenience kits: the Drape Pack (Model DYNJ35363A) and Sick Kids-General Custom Split (Model SPTPCD10005). While the products went through sterilization cycles, the calibration issues may have affected whether the products remained properly sterile.

Medline Industries identified calibration problems with equipment used to sterilize and package certain PPE Convenience Kits. Although the products went through sterilization, the equipment issues may have affected how well the sterility protection worked. Multiple lot numbers from 2021 through 2025 are involved.

Medline identified calibration problems with equipment used to sterilize and package their triple lumen insertion kits (Model DYNDM1031A). While the kits went through sterilization, the calibration issues may have affected whether they are truly sterile. This affects 15 units with lot number 23EBM150.

Medline identified calibration problems in the equipment used to sterilize and package DRAPE PACK-CHOICE kits (Model DYNJ63118A). While the products went through sterilization cycles, the equipment calibration issues may have affected whether the products are properly sterile.

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

Medline has recalled three models of burn care convenience kits because equipment used to sterilize and package them had calibration problems. While the products went through sterilization cycles, the calibration issues may have affected whether the kits are properly sterile. No injuries have been reported.