Class I · High risk
Sucralfate Oral Suspension
Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.
National Drug Code
Is NDC 66689-0305-16 recalled?
Sucralfate · 1 BOTTLE, PLASTIC in 1 CARTON (66689-305-16) / 414 mL in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
2 FDA recalls name the code 66689-0305-16 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
- Sucralfate
- Strength
- SUCRALFATE 1 g/10mL
- Form
- Suspension · Oral
- Labeler
- VistaPharm, LLC
- Type
- Human Prescription Drug
- Product code
- 66689-0305
Recalls naming this package
Class II · Moderate risk
Sucralfate Oral Suspension 1g per 10mL
Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
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
- 66689-0037 See recall 5
- 66689-0008 See recall 4
- 66689-0023 See recall 3
- 66689-0031 See recall 3
- 66689-0036 See recall 3
- 66689-0038 See recall 3
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