Class I · High risk
CLINIMIX E 5/15 sulfite-free
Presence of Particulate Matter: identified as dried skin.
National Drug Code
Is NDC 0338-1123-04 recalled?
Clinimix E · 2000 mL in 1 BAG (0338-1123-04)
Yes — this exact package was recalled
1 FDA recall names the code 0338-1123-04 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose
- Strength
- LEUCINE 365 mg/100mL; PHENYLALANINE 280 mg/100mL; LYSINE…
- Form
- Injection · Intravenous
- Labeler
- Baxter Healthcare Company
- Type
- Human Prescription Drug
- Product code
- 0338-1123
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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