Aspiration Catheter Recall: Q’Apel Medical, Inc. Removes Hippo 072 Aspiration System and Cheetah Delivery Tool After FDA Warning Letter About Internal Processes and Distal Tip Characteristics

Maquet is updating Servo Ventilator instructions due to a risk of inaccurate tidal volume delivery when the extended leak test is used.

CGMP/Finished Pharmaceuticals/Adulterated

IKM of San Jose, California is recalling the following cookware items because they may be contaminated with significant levels of lead (Pb) which may leach into food.

The differential pressure sensor in certain Impella devices may malfunction and cause sensor values to drift.

Joint US FDA – Health Canada ICH Public Meeting

This listing includes accelerated approvals (AAs) for malignant hematology and oncology indications with postmarketing trials that have verified clinical benefit and for which traditional approval has been subsequently granted for the specific indication.