Retractable Technologies recalls EasyPoint 25G needles due to potential detachment risk during medical procedures. Affected units have specific model and lot numbers.
The needle cannula of a retractable needle may detach from the needle holder in the patient.
Retractable Technologies is recalling EasyPoint 25G needles that may detach from the needle holder during use, which could cause injury. This recall affects medical devices used in procedures requiring precise needle insertion.
The needle cannula may detach from the needle holder while being used on a patient. This detachment could lead to the needle moving unexpectedly, potentially causing injury. The risk occurs during the procedure when the needle is in contact with the patient.
Healthcare professionals using the EasyPoint needles for medical procedures are most at risk. Patients receiving these needles during procedures could be affected if the needle detaches.
Check for EasyPoint needles with model number 25G x 5/8" and reference number 82091. The lot number K220402 and expiration date 03/28/2027 are also associated with this recall.
Verify the model number (25G x 5/8"), reference number (82091), lot number (K220402), and expiration date (03/28/2027) to confirm if your needle is affected.
The recall states the needle cannula may detach during use, which could cause injury. However, the remedy is not specified, so users should check details before proceeding.
Check for model number 25G x 5/8", reference number 82091, lot number K220402, and expiration date 03/28/2027.
The recall does not specify a remedy, so users should check the details to confirm if their needle is affected and contact the manufacturer if needed.
We’ve drafted a message you can send Retractable Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1293-2024 — Retractable Technologies Retractable Technologies Hello, I own a Retractable Technologies that is covered by recall Z-1293-2024 from Retractable Technologies. 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.
