Class III · Low risk
DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose
Temperature Abuse: Product exposed to temperature outside specified limits.
National Drug Code
Is NDC 49230-0209-30 recalled?
Delflex · 4 BAG in 1 CARTON (49230-209-30) / 3000 mL in 1 BAG
Yes — this exact package was recalled
2 FDA recalls name the code 49230-0209-30 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
- Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride
- Strength
- DEXTROSE MONOHYDRATE 2.5 g/100mL; SODIUM CHLORIDE 538…
- Form
- Solution · Intraperitoneal
- Labeler
- Fresenius Medical Care Renal Therapies Group, LLC
- Type
- Human Prescription Drug
- Product code
- 49230-0209
Recalls naming this package
Class III · Low risk
DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose
Temperature Abuse: Product exposed to temperature outside specified limits.
Class II · Moderate risk
DELFLEX Peritoneal Dialysis Solution
Lack of Assurance of Sterility: Leakage of the peritoneal dialysis (PD) solution 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
- 49230-0300 Sodium Chloride 5
- 49230-0206 Delflex 4
- 49230-0212 Delflex 3
- 49230-0188 Delflex 1
- 49230-0530 Venofer 1
- 49230-0534 Venofer 1
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