URGENT MEDICAL DEVICE CORRECTION
BD is conducting a voluntary medical device recall of 3ml Luer-Lok Syringes and 3ml Safety-Lok Syringes
B. Braun Medical Inc. (BBMI) is issuing a voluntary medical device recall of Rate Flow® Regulator Administration sets due to reported deficiencies in the manufacturer's quality systems at its manufacturing facility. Rate Flow Regulator Administration sets are manufactured by Leventon S.A.U. and purchased as a finished product by BBMI.
Typo on the expiration date of the primary package (Tyvek) which affects an unknown quantity of the lot produced
BD has announced a voluntary recall of certain lot numbers of several PosiflushTM Heparin Lock Syringes and Pre-filled Saline Syringes.
CADD® Non Flow-Stop Medication Cassette Reservoirs
URGENT MEDICAL DEVICE FIELD SAFETY NOTICE
URGENT PRODUCT RECALL
Vyaire Medical Corrective Action; 0.9% Sodium Chloride Solution
Bard Medical has initiated a voluntary product recall of specific Bard Irrigation Syringes.
Secure pharmacy compounding devices (AutoCOMP6, AutoCOMP6 XP, AutoCOMP6 XPS) and the SECURE Compounder Bags
Triton and Triton fp Infusion pumps (model 30000 and 40000)
Field Corrective Action
RMS Flow Rate Tubing; Safety Needle Sets