April 4, 2001Steris Laboratories Recalls
Vercuronium Bromide Injection
AZ (SafetyAlerts) - The Food and
Drug Administration (FDA) said today that Steris Laboratories, Inc. has recalled
Vercuronium Bromide Injection because of a lack of assurance of sterility-filter
This is the first public notice of
this Class II
recall issued by FDA.
Vercuronium Bromide Injection, 10 mg, 1 mg/ml.
Lot 99M090 Schein Pharmaceutical (NDC 0364-3061-33)
Lot 99M130 Schein Pharmaceutical (NDC 0364-3062-33)
Lot 99N140 American Pharmaceutical Partners (NDC 63323-414-10)
Steris Laboratories, Inc., Phoenix, AZ.
Manufacturer, by letters on 02/12/01. Firm-initiated recall
AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MA, ME, MN, MO, MS, NC, ND, NJ, NM, NY,
OH, OR, PA, SC, TN, TX, UT, WA, WI, WV, Puerto Rico and Canada.
36510 lot 99M090, 48150 lot 99M130, 47110 lot 99N140.
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.