Class II · Moderate risk
Succinylcholine Chloride Injection
Lack of Sterility Assurance
National Drug Code
Is NDC 0409-6629-02 recalled?
Quelicin · 25 VIAL, MULTI-DOSE in 1 TRAY (0409-6629-02) / 10 mL in 1 VIAL, MULTI-DOSE (0409-6629-12)
Yes — this exact package was recalled
3 FDA recalls name the code 0409-6629-02 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.
1 of these recalls is still ongoing.
- Active ingredient
- Succinylcholine Chloride
- Strength
- SUCCINYLCHOLINE CHLORIDE 20 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-6629
Recalls naming this package
Class III · Low risk
Quelicin (Succinylcholine Chloride)
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label on the glass vial.
Class II · Moderate risk
QUELICIN (succinylcholine chloride)
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
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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