Recall of SOLOPATH Balloon Expandable TransFemoral System and Re-Collapsible Balloon Access System by Terumo Medical Corporation due to dislodgement of the fairing tip from the sheath.
Heritage Pharmaceuticals issued a voluntary recall of specific lots of amikacin sulfate and prochlorperazine edisylate injections on May 28, 2019, due to possible lack of sterility.
Recall of amikacin sulfate injection, USP 1gm/4 mL (250mg/mL) and prochlorperazine edisylate injection, USP 10mg/2mL (5mg/mL) by Heritage Pharmaceuticals due to sterility test failure.
Recall of LimiTorr Volume Limiting CSF Drainage System and the MoniTorr ICP External CSF Drainage and Monitoring System by lntegra LifeSciences due to possible breakage.
Recall of DxH 800, DxH 600, and DxH 900 hematology analyzers by Beckman Coulter Life Sciences due to sporadic erroneously elevated platelet count results without flags or system messages.
FDA issued recall of losartan potassium 25 mg, 50 mg and 100 mg tablets by Vivimed Life Sciences due to trace amounts of n-nitroso-n-methyl-4-aminobutyric acid (NMBA) impurity.