Class II · Moderate risk
DELFLEX PERITONEAL DIALYSIS SOLUTION With LOW MAGNESIUM / LOW…
This product is being recalled due to the tube weld failure presents itself as a slow leak and can be difficult to detect.
National Drug Code
Is NDC 49230-0212-50 recalled?
Delflex · 2 BAG in 1 CARTON (49230-212-50) / 5000 mL in 1 BAG
Yes — this exact package was recalled
1 FDA recall names the code 49230-0212-50 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.
1 of these recalls is still ongoing.
- Active ingredient
- Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride
- Strength
- DEXTROSE MONOHYDRATE 4.25 g/100mL; SODIUM CHLORIDE 538…
- Form
- Solution · Intraperitoneal
- Labeler
- Fresenius Medical Care Renal Therapies Group, LLC
- Type
- Human Prescription Drug
- Product code
- 49230-0212
Recalls naming this package
Class III · Low risk
DELFLEX Peritoneal Dialysis Solution with 4.25% Dextrose
Temperature Abuse: Product exposed to temperature outside specified limits.
Class III · Low risk
DELFELX Peritoneal Dialysis Solution with 4.25% Dextrose
Temperature Abuse: Product exposed to temperature outside specified limits.
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
- 49230-0209 Delflex 3
- 49230-0188 Delflex 1
- 49230-0530 Venofer 1
- 49230-0534 Venofer 1
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