Class II · Moderate risk
Haloperidol Decanoate Injection
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
National Drug Code
Is NDC 68001-0580-41 recalled?
Haloperidol Decanoate · 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-580-41) / 1 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
2 FDA recalls name the code 68001-0580-41 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.
2 of these recalls are still ongoing.
- Active ingredient
- Haloperidol Decanoate
- Strength
- HALOPERIDOL DECANOATE 50 mg/mL
- Form
- Injection · Intramuscular
- Labeler
- BluePoint Laboratories
- Type
- Human Prescription Drug
- Product code
- 68001-0580
Recalls naming this package
Class II · Moderate risk
Haloperidol Decanoate Injection 50mg/mL
Lack of Assurance of Sterility: Media fill with bacterial contamination
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
- 68001-0414 See recall 3
- 68001-0415 See recall 3
- 68001-0581 Haloperidol Decanoate 3
- 68001-0264 See recall 2
- 68001-0313 Azacitidine 2
- 68001-0501 Metoprolol Succinate 2
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