Class II · Moderate risk
Linezolid Injection 600 mg per 300 mL
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
National Drug Code
Is NDC 55150-0242-51 recalled?
Linezolid · 10 POUCH in 1 CARTON (55150-242-51) / 1 BAG in 1 POUCH / 300 mL in 1 BAG
Yes — this exact package was recalled
2 FDA recalls name the code 55150-0242-51 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
- Linezolid
- Strength
- LINEZOLID 600 mg/300mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Eugia US LLC
- Type
- Human Prescription Drug
- Product code
- 55150-0242
Recalls naming this package
Class I · High risk
Linezolid Injection 600 mg/300 mL
Presence of Particulate Matter; white particulate matter identified as mold was found in one bag
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
- 55150-0120 Piperacillin and Tazobactam 2
- 55150-0183 Nicardipine Hydrochloride 2
- 55150-0202 Pantoprazole Sodium 2
- 55150-0243 Levofloxacin 2
- 55150-0306 Progesterone 2
- 55150-0113 Ampicillin 1
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