Class I · High risk
Fentanyl Citrate
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).
National Drug Code
Is NDC 61553-0107-50 recalled?
Fentanyl Citrate
Yes — this exact package was recalled
1 FDA recall names the code 61553-0107-50 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
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
- 61553-0197 See recall 3
- 61553-0284 See recall 3
- 61553-0287 See recall 3
- 61553-0103 See recall 2
- 61553-0119 See recall 2
- 61553-0127 See recall 2
Free recall alerts
Know the day your medication is recalled
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