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SafetyAlerts
November 12,  2003

Braintree Laboratories Medical Has Recalled NuLYTELY

(SafetyAlerts) - The FDA has released the following information.

PRODUCT
a) NuLYTELY, Powder for Reconstitution, (PEG 33350, Sodium
Chloride, Sodium Bicarbonate and Potassium Chloride for
Oral Solution), Rx only, disposable jug.
Recall # D-041-4;
b) NuLYTELY, Powder for Reconstitution, Cherry Flavor,
(PEG 33350, Sodium Chloride, Sodium Bicarbonate and
Potassium Chloride for Oral Solution), Rx only,
Disposable jug. Recall # D-042-4;
c) NuLYTELY, Powder for Reconstitution, Lemon-Lime
(PEG 33350, Sodium Chloride, Sodium Bicarbonate and
Potassium Chloride for Oral Solution), Rx only,
disposable jug. Recall # D-043-4;
d) NuLYTELY, Powder for Reconstitution, Orange Flavor,
(PEG 33350, Sodium Chloride, Sodium Bicarbonate and
Potassium Chloride for Oral Solution), Rx only,
disposable jug. Recall # D-044-4.

CODE
a) Lot Number: N3E005 Exp. Date: 5/06;
b) Lot Number: C3G020 Exp. Date: 7/05;
c) Lot Number: L3F014 Exp Date: 6/05;
d) Lot Numbers: R3G011 Exp. Date: 7/05 and R3E009,
Exp. Date: 5/05.

RECALLING FIRM/MANUFACTURER
Braintree Laboratories, Inc., Braintree, MA, by letter dated September 25, 2003. Firm initiated recall is ongoing.

REASON
Product overfill: double one ingredient (PEG-3350).

VOLUME OF PRODUCT IN COMMERCE
69,744 bottles.

DISTRIBUTION
Nationwide
.

 
Selected Recent Recalls


Health Professional:

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

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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.