Lumicell recalls 900-00218 Sterile Cover 10-Pack Shipper Box Assembly due to potential elastic band detachment during surgery, which could lead to retained foreign bodies and infections.
The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a risk of retained foreign bodies in the surgical cavity and potentially leading to surgical site infections.
Lumicell is recalling its 900-00218 Sterile Cover 10-Pack Shipper Box Assembly because elastic bands might detach or fracture during surgery. This could leave foreign objects inside the surgical site, increasing infection risk.
The elastic bands in the sterile cover could detach or fracture during surgery. If this happens, foreign material might remain inside the surgical site, potentially causing infections.
Healthcare professionals using the sterile cover during surgical procedures are most at risk. Patients undergoing surgery with this product may face infection complications.
Check for the model number 900-00218 on the sterile cover packaging. The product was sold with lot numbers 43930 through 44349-04.
Look for the model number 900-00218 on the sterile cover packaging or the lot numbers listed in the recall notice.
The recall states that the elastic bands could detach or fracture during surgery, which might lead to infections. If you have this product, you should check the recall details.
The recall does not specify a remedy, so you should check the official recall notice for further instructions.
Check the model number on the packaging; affected products have the model number 900-00218 with lot numbers 43930 through 44349-04.
We’ve drafted a message you can send Lumicell to request your refund or repair — edit it as you like.
Subject: Recall Z-2519-2025 — Lumicell Lumicell Hello, I own a Lumicell that is covered by recall Z-2519-2025 from Lumicell. 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.
