These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
Probes may rupture/burst during activation
Erbe USA recalled 5,154 Flexible Cryoprobes used in surgery after probes may rupture during activation. The defect can cause rupture or burst during activation. Stop using the device and follow recall instructions from the manufacturer.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Probes may rupture/burst during activation
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
SOOWERY recalled 50,000 6-Drawer Dressers on February 12, 2026, due to tip-over and entrapment hazards. The dressers can cause serious injuries or death if not anchored to the wall. Consumers should stop using the dressers immediately if they are not anchored.
Product Contains undeclared FD&C Yellow #5 & #6 and Red #40
CheerKid recalled baby bath seats on February 12, 2026, due to drowning risks. The seats can tip over, violating safety standards. Parents should stop using them immediately and seek a refund.
Surveying Accessories Cheaper recalled Colombia-themed magnetic board games on February 12, 2026. The games pose a high risk of serious injury or death from magnet ingestion. Consumers should stop using the games immediately and seek a refund.
LShome recalled 3-Pack Smoke Detector Fire Alarms on February 12, 2026, due to a failure to warn during a fire. The defect poses a serious risk of injury or death. Consumers should stop using these alarms immediately and contact the manufacturer for a refund.
Slate Run Pharmaceuticals recalled Eptifibatide Injection on February 12, 2026. The recall affects all lots of the 75 mg/100 mL vial due to incorrect dosing information. Healthcare providers and consumers must stop using the product immediately.
Potential for attenuation degradation over time, decreasing the lifespan.
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units