Georgia recalls

Taro Pharmaceuticals is recalling specific lots of fluocinolone acetonide topical solution (0.01%) because testing found higher-than-allowed levels of an impurity. The affected lots were distributed nationwide. No injuries have been reported.

Suzanna's Kitchen recalled approximately 13,720 pounds of ready-to-eat grilled chicken breast fillets produced on October 14, 2025, because they may contain Listeria monocytogenes bacteria. The contamination was found during routine lab testing. No illnesses have been reported so far.

Frigidaire-brand minifridges sold at Target can overheat and catch fire due to faulty electrical components. Curtis International has received six reports of fires in the EFMIS121 model, with property damage. The recall now includes about 330,000 additional units across five model numbers.

RootStim Beard Growth Serum spray bottles contain minoxidil, a powerful medication that must be in child-resistant packaging by law. These bottles do not have child-resistant caps, creating a serious risk of poisoning if a young child swallows the liquid. The product was sold online from November 2024 through September 2025.

Greatale self-feeding pillows can hold a bottle at an unsafe angle that an infant cannot pull away from, risking aspiration of milk or formula and suffocation. About 1,260 pillows were sold online through Amazon between September 2024 and July 2025.

HEZI brand power strips with gray or yellow metal enclosures can cause serious electric shock or death if the metal case becomes energized. The strips lack proper grounding and were sold online from May 2024 through October 2025. No injuries have been reported yet, but the risk is serious.

Morgan Lane Asher Pajama Sets (Style 816TR in Petal, sizes 2T–14) fail to meet federal flammability standards for children's sleepwear and pose a serious burn hazard. These cotton pajamas with tiny rose prints were sold online from March 2024 through May 2025.

Adams Manufacturing recalled Adirondack-style resin patio chairs sold at Lowe's and Home Depot because they can crack and collapse during use, creating a fall and injury risk. About 6,100 chairs are affected, sold from August through October 2025 in multiple colors.

KEAWIS crib mattresses (model XX-BM-01) may not fit properly in certain play yards or smaller cribs, creating dangerous gaps where babies can become trapped or suffocate. The mattresses do not meet federal safety standards for crib mattresses. About 1,500 units were sold online through Amazon between August 2024 and July 2025.

R.X.Y-branded adult bicycle helmets sold on Amazon do not meet federal safety standards for impact protection and stability. In a crash, these helmets may fail to protect your head, creating a serious risk of injury or death.

BBWOO baby loungers have sides that are too low to safely contain an infant and openings that are wider than safety standards allow, creating fall and entrapment hazards. The loungers also lack a stand, which can cause them to fall if placed on elevated surfaces. These design flaws violate mandatory infant sleep product safety standards.

Energizer is recalling about 4,100 Large Power Indicator Lanterns (model BGAAL9) with June 2024 date codes because the lithium-ion batteries can overheat and cause burns. One overheating incident has been reported, though no injuries so far.

Ruahouine Hair Growth Serum bottles contain minoxidil, a powerful chemical that can cause serious poisoning if swallowed. The bottles do not have child-resistant caps as required by law, making it easy for young children to open and ingest the contents. About 25,000 bottles were sold on Amazon between January and July 2025.

The 14-gauge Tuohy needle included in certain Codman CereLink ICP Sensor Basic Kits may have corrosion stains on its surface. These kits are used by hospitals and surgical centers for monitoring intracranial pressure during brain procedures. Integra LifeSciences is recalling specific lot numbers distributed worldwide.

Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.

Medline Industries is recalling multiple models of Hudson RCI oxygen masks because the tubing can disconnect during use. If this happens, oxygen delivery stops, which can delay patient care and cause breathing problems that may require medical intervention.

The torque screw in certain IMRIS HFD100 Head Fixation Devices may crack or separate during use. This could cause the device to fail to hold a patient's head securely during surgery, potentially affecting surgical accuracy and requiring emergency use of backup fixation methods.

Philips MX40 patient monitors may lose wireless connection to the PIC iX central station when moving between certain access points if the signal strength changes rapidly. This could interrupt patient data transmission to clinical staff.

Securitas Healthcare identified a firmware problem in certain Arial 900 MHz Call Station units (Model CSK200-900MR, Firmware 1.6.3) sold between January 2023 and June 2024. The affected units may fail to send a low battery alert to the wireless system before the battery dies, or may not send the alert at least 7 days in advance as designed. This could leave the call station without power when someone needs to use it.

A firmware issue in certain Securitas Healthcare Arial 900 MHz call stations (Model CSK200-900) may prevent them from sending low battery warnings to the wireless system. This means the device could lose power without giving you advance notice. The affected units were sold between January 1, 2023 and June 26, 2024.

Abiomed has recalled 2 units of the Impella 5.5 with SmartAssist S2 heart pump device because the devices were shipped in incorrect outer box cartons. This packaging error may affect proper device identification and handling. No injuries have been reported.

Sophysa's Pressio 2 ICP Monitoring System (Model PSO-4000) may unexpectedly reboot during use. This device is used in hospitals to measure pressure inside the skull. The reboots could interrupt critical monitoring of patients.

A software issue in certain BD Pyxis ES Enterprise Server systems may prevent timely updates of patient, medication, and related information from reaching the dispensing cabinets. This could delay access to critical data in healthcare settings. BD and the FDA are working to address the problem.

Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If healthcare providers base clinical judgment on unvalidated measurements, this could potentially lead to incorrect clinical decisions.

Beckman Coulter UniCel Dxl 800 analyzers (part numbers 973100, A71456, A71457, A25288) may fail to restart after shutdown due to a communication issue. When this happens, the analyzer cannot initialize or process patient samples, QCs, or calibrators, which delays test results.

Certain Beckman Coulter UniCel DxL 600 analyzers may fail to restart properly after shutdown due to a communication issue. When this happens, the analyzer cannot process patient samples or quality control checks, which can delay test results.

Meridian Bioscience's Revogene C. difficile diagnostic test (a lab assay used with the Revogene instrument) may show declining accuracy over time in certain lots. This could produce false-negative results, meaning the test might not detect C. difficile infection when it is present.

Roche Diagnostics has recalled certain lots of the Elecsys Anti-TSHR blood test due to inconsistent results across different laboratory instruments and variations between calibrator batches. These issues could lead to incorrect or delayed thyroid diagnosis and treatment.

Philips Healthcare has recalled certain Incisive CT scanners due to an unstable internal connection in the floating sensor. This instability may cause the scanner to produce incomplete or compromised scans. The issue affects 35 devices distributed across the U.S. and its territories, and no injuries have been reported.

AVID Medical is recalling the Halyard MINI PLUS KIT SOUTH (Kit Code JACK097-08) because the devices are not suitable for organ transplant procedures. The recall affects 380 units distributed in Florida, Georgia, and Puerto Rico.