Alerts

Recall of all manufactured products by Mavidon due to contamination.

Increased risk of respiratory depression when using gabapentin or pregabalin.

Recall of VNS Therapy SenTiva Generator System by LivaNova due to error.

Recall of levetiracetam oral solution by Lannett Company due to contamination.

Recall of Medfusion 4000 Syringe Pumps by Smiths Medical ASD due to malfunction.

Recall of ranitidine tablets by Glenmark Pharmaceuticals due to impurity.

Recall of Giraffe Incubators and OmniBeds by GE Healthcare due to fall potential.

Recall of CrossCath support catheters by Cook Medical due to manufacturing error.

Recall of SynchroMed II implantable drug infusion pump by Medtronic due to potential presence of foreign particles.

Recall of drugs, dietary supplements and devices by Basic Reset and Biogenyx due to federal violations.

Recall of blood administration sets by B. Braun Medical due to leakage.

Recall of ranitidine tablets (150mg and 300mg) and ranitidine syrup (15 mg/mL) by Amneal Pharmaceuticals due to impurity.

Recall of ranitidine oral solution, USP 150 mg/10 mL by Precision Dose due to impurity.

Recall of ranitidine capsules by Golden State Medical Supply due to impurity.

Recall of Silver Bullet 10 male enhancement capsules by Nature’s Rx due to undeclared sildenafil.

Recall of ranitidine tablets, 150mg and 300mg, and ranitidine syrup (oral solution), 15 mg/mL by Amneal Pharmaceuticals due to impurity.

Recall of Up2 by Med Man Distribution due to undeclared sildenafil.

Recall of ranitidine syrup, 150 mg/10 mL by American Health Packaging due to impurity.

Recall of 38 Lots of ranitidine tablets, capsules, and syrup by Aurobindo Pharma USA due to impurity.

Recall of ROSA Brain 3.0 robotic surgery system by Zimmer Biomet due to software issue.

High concentrations of biotin in the blood can interfere with some laboratory tests leading to misinterpretation of test results and incorrect patient diagnoses.

Recall of MiniMed Insulin Pumps by Medtronic due to potential cybersecurity risks.

Recall of CentriMag Circulatory Support System Motor by Abbott Recall due to a calibration system error resulting from electromagnetic interference that may cause the pump to slow or stop, the...

Recall of Forte Gamma Camera System by Philips Medical Systems (Cleveland) due to potential detachment.