stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Roche Diagnostics Recalling Anti-TSHR Immunoassay Over Diagnosis Risk
Roche Diagnostics Operations recalled 1,300 Anti-TSHR immunoassay cassettes on November 21, 2025. Variability in results may lead to incorrect diagnoses and treatment delays. The recall affects multiple states across the U.S.
SB FOOD Recalls Gummy Candy Over Unallowed Color Additive
SB FOOD recalled 100 cases of Yoyo Gummy Assorted Flavor on November 21, 2025. The product contains an unapproved color, Carmoisine (E122), posing health risks. Consumers should not consume the candy and seek refunds.
Medtronic Recalls Clinician Programmer App Over High-Risk Software Issue
Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.
CareFusion 303 Recalls Automated Dispensing Cabinets Due to Error Risk

Romorgniz 12- and 13-Drawer Dressers Recalled for Tip-Over Hazard After STURDY Act Violation (2025)

Spartan Mowers Recalls 2025 SRT-XD and KGZ-XD Riding Mowers for Steering Damper Hazard

Anzmtosn 15-Piece Magnet Fidget Spinner Sets Recalled for Ingestion Risk (2025)

Little Partners Recalls Grow 'N Stow Folding Learning Tower Over Fall Hazard (2025)

Demlar Recalls MoonSoll and Magic Chems Fuel Bottles Over Flash Fire Risk (2025)



Mallimoda Children's Pajama Sets Recalled Over Burn Hazard in 2025
Mallimoda recalled its children’s pajama sets sold on Amazon due to a burn hazard risk. The recall cites violations of mandatory sleepwear standards. Consumers should stop using the recalled sets and contact Mallimoda for a full refund.
Fagron Compounding Services Recalls Ophthalmic Solution Over Incorrect Formulation

Steris Washers Recalled Due to Electrical Arcing Hazard
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
Sonex Aluminum Pot Recall: 2 Units for Lead Leaching (2025)
Products found to contain leachable lead levels (0.323mg/L)
Vortex Surgical Recalls Laser Probe Due to Smooth Passage Issues
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Glenmark Pharmaceuticals Recalls Nebivolol Tablets Over Contamination
Cross Contamination with Other Products
AGFA Recalls Digital Radiography X-Ray System Over Radiation Risk
It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on the NX workstation when ABS is not enabled.