Medical Action Industries recalls Port Access Kits with incorrect IV Start Kit labeling. This labeling error may cause confusion in medical use. Affected kits have specific lot numbers and expiration dates.
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
Medical Action Industries is recalling Port Access Kits that were incorrectly labeled as IV Start Kits. This labeling error could lead to confusion during medical procedures, potentially causing incorrect use of the kit.
The Port Access Kits were mislabeled as IV Start Kits on the kit label, which could lead to confusion about the correct use. This error might result in using the wrong type of kit during medical procedures.
Healthcare professionals using these kits during medical procedures are most at risk. Patients receiving care with the incorrectly labeled kits may be affected.
Check the case label for lot number 294281 (exp. 9/28/2023) or lot number 294589 (exp. 12/20/2024). The kits are sterile and labeled as either Port Access Kits or IV Start Kits.
Look for the case label with lot number 294281 (exp. 9/28/2023) or lot number 294589 (exp. 12/20/2024).
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label, which could cause confusion during medical procedures.
Check the case label for lot numbers 294281 or 294589 to determine if it's affected. If it is, contact Medical Action Industries for guidance.
The labeling error could lead to incorrect use, but the recall is for labeling issues, not a safety hazard.
We’ve drafted a message you can send Medical Action Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0464-2023 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-0464-2023 from Medical Action Industries. 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.
