notyard
04-14-2009, 02:37 PM
FDA class I recall:
PRODUCT
20 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL Flexible Plastic Containers, Rx only, NDC 0409-7902-09. Recall # D-197-2009
CODE
Lot number: 65-620-FW
RECALLING FIRM/MANUFACTURER
Recalling Firm: Hospira, Inc, Lake Forest, IL, by letters on September 18, 2008.
Manufacturer: Hospira, Inc, Rocky Mount, NC. Firm initiated recall is ongoing.
REASON
Labeling; Incorrect Bar Code; some of the bags may be incorrectly labeled with a bar code that indicates 5% Dextrose Injection, USP.
VOLUME OF PRODUCT IN COMMERCE
70,860 bags
DISTRIBUTION
Nationwide
PRODUCT
20 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL Flexible Plastic Containers, Rx only, NDC 0409-7902-09. Recall # D-197-2009
CODE
Lot number: 65-620-FW
RECALLING FIRM/MANUFACTURER
Recalling Firm: Hospira, Inc, Lake Forest, IL, by letters on September 18, 2008.
Manufacturer: Hospira, Inc, Rocky Mount, NC. Firm initiated recall is ongoing.
REASON
Labeling; Incorrect Bar Code; some of the bags may be incorrectly labeled with a bar code that indicates 5% Dextrose Injection, USP.
VOLUME OF PRODUCT IN COMMERCE
70,860 bags
DISTRIBUTION
Nationwide