Braun, B Medical Inc 18G Catheter is a component in various kits. Recall

Check Your Product

According to the U.S. Food and Drug Administration (FDA)

Reason for Recall

As stated by FDA

Catheter separated from the hub.

Recommended Action

Per FDA guidance

The recalling firm issued a recall notification letter on March 19, 2004 to their direct accounts. The letter identified the problem and instructs the direct account to destroy individual units but return unopened cases to the recalling firm.

Distribution

As reported by FDA

CA, CO, FL, GA, IL, IN, LA, MD, MA, MI, MN, MS, MO, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, VA, WV, WI, DC, PR