PlainRecalls
FDA Devices Moderate Class II Terminated

STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches

Reported: July 16, 2014 Initiated: May 29, 2014 #Z-2022-2014

Product Description

STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches

Reason for Recall

Complaints were received that reported the stopcock of some Stopcock Extension Sets are assembled in the reverse position, resulting in the stopcock being closed when set in the open position and vise versa.

Details

Recalling Firm
B. Braun Medical, Inc.
Units Affected
10,835
Distribution
USA (nationwide) including the states of PA, IL, NC, FL, IL, CA, CO, NE, LA, NC, LA, VA, TN, NE, TX, and KS.
Location
Allentown, PA

Frequently Asked Questions

What product was recalled?
STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches. Recalled by B. Braun Medical, Inc.. Units affected: 10,835.
Why was this product recalled?
Complaints were received that reported the stopcock of some Stopcock Extension Sets are assembled in the reverse position, resulting in the stopcock being closed when set in the open position and vise versa.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 16, 2014. Severity: Moderate. Recall number: Z-2022-2014.