I posted the recall information on the liquid in another thread below... but here it is again. The liquid DID NOT WORK!!! It is not mix well and then you are just giving the sugar to your child!!!
http://www.safetyalerts.com/recall/f/00/d216218.htm
SafetyAlerts
February 23, 2000
August 16, 2000
Cortef Oral Suspension Recalled
Kalamazoo, MI (
SafetyAlerts) - The Food and Drug Administration (FDA) stated in a report released yesterday that Pharmacia Corporation is conducting a recall of its Cortef Oral Suspension because the product may not always be effective for the treatment of congenital adrenal hyperplasia.This is the first public notice of this
Class II recall issued by the FDA.PRODUCT
Cortef(r) Oral Suspension (hydrocortisone cypionate) 10 mg/5mL, in 4 fluid ounce units. NDC #0009-0142-01.
Recall #D-447-0.
CODE
Lot numbers: 62CAT, 63CAT, 64CAT, 23CRW, 24CRW, 04CJX, 05CJX, 19DAJ, 98DXA and 91DTM.
MANUFACTURER
Pharmacia Corporation, Kalamazoo, Michigan.
RECALLED BY
Manufacturer, by letter dated July 18, 2000. Firm-initiated recall ongoing.
DISTRIBUTION
Nationwide, Belgium, Canada, Chile, Ireland, United Kingdom, Uruguay.
QUANTITY
144,357 bottles were distributed.
Questions concerning these recalls may be directed to the FDA at 1-888-INFO-FDA.
Pharmacia & Upjohn Recall Solu-Cortef Products
Kalamazoo, MI (
SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Pharmacia & Upjohn is recalling certain Solu-Cortef products because of a lack of assurance of sterility.The recalled Solu- Cortef Hydrocortisone sodium succinate for injection, USP, comes in 100 mg, single dose vials with 2mL sterile powder. NDC0009-0900-20 has the Lot number of 29DAM EXP 3/31/04, NDC0009-0900-13 has the lot number of 48DCU EXP 6/30/04 and NDC0009-0912-05 has the Lot numbers of 51DCU and 52DCU EXP 6/30/04.
According to FDA, about 261,000 vials were distributed nationwide as well as in the Bahamas, Cayman Islands, Colombia and Japan.
This ongoing
Class II recall was initiated by Pharmacia & Upjohn, by letter dated January 27, 2000.This is the first public notice issued by the FDA. Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.