Repro-Med recalls 20" 2-needle 26-gauge subcutaneous safety needle sets with mislabeled lengths. Affected units may have incorrect needle lengths, potentially causing injury during medical use.
Mislabeled needle lengths
Repro-Med is recalling 20-inch 2-needle 26-gauge subcut: safety needle sets due to mislabeled needle lengths. This could lead to incorrect needle depth during medical procedures, increasing injury risk.
Mislabeled needle lengths could result in needles being too short or too long for the intended subcutaneous tissue. This might cause improper medication delivery or tissue injury during injections.
Healthcare professionals using these needle sets for subcutaneous medication delivery. Those with the specific product model and lot number are most at risk.
Check for product # RMS22606 with lot number N.78648. These are 20-inch 2-needle 26-gauge subcutaneous safety needle sets used for medication delivery.
Verify the product number (RMS22606) and lot number (N.78648) on the packaging.
The needle sets have mislabeled lengths, which could lead to incorrect needle depth during medical procedures.
Look for product # RMS22606 with lot number N.78648 on the packaging.
The recall record does not specify a remedy, so no action is required beyond checking the product details.
We’ve drafted a message you can send Repro-Med to request your refund or repair — edit it as you like.
Subject: Recall Z-0051-2020 — Repro-Med Repro-Med Hello, I own a Repro-Med that is covered by recall Z-0051-2020 from Repro-Med. 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.
