Windstone Medical recalls Aligned Hand Pack REF AmS460: P2 Cover Light Handle Blue STE may detach during use, risking procedure delays or patient injury. Affected units contain Lot 188843.
Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient
Windstone Medical is recalling Aligned Medical Solutions Hand Packs with the reference number AmS4601E because the blue cover light handle may detach during use. This could delay medical procedures or cause patient injuries by compromising the sterile field.
The blue cover light handle may detach from the light handle during use. If it falls off, it could disrupt the sterile field and delay medical procedures, potentially leading to patient injuries.
Healthcare professionals using the Aligned Medical Solutions Hand Packs for procedures are most at risk. Patients undergoing surgery or medical treatments with these devices could be affected if the handle detaches.
Check for the reference number AmS4601E on the packaging. The product contains Lot 188843 and UDI: B098AMS4601E0. This recall applies to the specific hand pack model used in medical procedures.
Look for the reference number AmS4601E and lot number 188843 on the packaging.
The blue cover light handle may detach during use, which could delay procedures or cause patient injuries by compromising the sterile field.
Check for the reference number AmS4601E and lot number 188843 on the packaging.
The recall record does not specify a remedy, so contact the manufacturer for guidance.
We’ve drafted a message you can send Windstone Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1621-2023 — Windstone Medical Windstone Medical Hello, I own a Windstone Medical that is covered by recall Z-1621-2023 from Windstone Medical. 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.
