Sodium Chloride · 48 POUCH in 1 CASE (0990-7984-23) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
Recall announced for this productannounced by the firm and posted by FDA; not yet in FDA’s classified recall data
0.9% Sodium Chloride Injection, USP, 100 mL· Otsuka ICU Medical LLC · Reason Product mix-up where 0.9% Sodium Chloride Injection, USP overwrap may contain 10 mEq Potassium Chloride Injection
Yes — this exact package was recalled
1 FDA recall names the code 0990-7984-23 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.
Product Mix-up: 0.9% SODIUM CHLORIDE Injection, USP may potentially contain the overwrap with labeling indicating it to be 0.9% SODIUM CHLORIDE Injection, USP but the actual product within the overwrap may be POTASSIUM CHLORIDE Inj.10 mEq
OngoingLabeling / mix-upOtsuka ICU Medical LLCNDC 0990-7984-23Recall number pending
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.
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.