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SafetyAlerts
April 4, 2001

Steris Laboratories Recalls Vercuronium Bromide Injection

Phoenix, 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 validation.

This is the first public notice of this Class II recall issued by FDA.

PRODUCT
Vercuronium Bromide Injection, 10 mg, 1 mg/ml.

Recall #D-149-1.

CODE:
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)

MANUFACTURER:
Steris Laboratories, Inc., Phoenix, AZ.

RECALLED BY:
Manufacturer, by letters on 02/12/01. Firm-initiated recall
ongoiing.

DISTRIBUTION:
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.

QUANTITY:
36510 lot 99M090, 48150 lot 99M130, 47110 lot 99N140.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.