Ritedose recalls 23.4% Sodium Chloride Injection with incorrect barcode labeling that may cause confusion with rocuronium bromide. Affected products have specific NDC and batch numbers.
Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.
Ritedose is recalling a specific type of saline injection due to a barcode error that could lead to confusion with a different medication. This mistake might cause incorrect use if the product is mistaken for rocuronium bromide injection.
The product's barcode incorrectly identifies it as rocuronium bromide injection instead of sodium chloride injection. This could lead to confusion during medication administration, potentially causing incorrect treatment if the wrong product is used.
Healthcare professionals who use this saline injection for medical purposes may be affected. Patients receiving the product under a prescription are at risk if the wrong medication is administered due to labeling confusion.
Check for the product name '23.4% Sodium Chloride Injection, 120 mEq per 30 mL' on the label. Look for NDC number 65302-509-30 and batch numbers 210137-01, 220026-01, or 220050-01.
Verify the product name and NDC number to ensure it matches the correct saline injection.
The product is safe if used correctly, but the labeling error could cause confusion with another medication. Always check the label before use.
The recall does not specify a remedy, so check the label and contact the manufacturer if you have concerns.
Look for NDC number 65302-509-30 and batch numbers 210137-01, 220026-01, or 220050-01 on the label.
We’ve drafted a message you can send Ritedose to request your refund or repair — edit it as you like.
Subject: Recall D-0745-2022 — Ritedose Ritedose Hello, I own a Ritedose that is covered by recall D-0745-2022 from Ritedose. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
