Ecolab recalls Camera Arm Drape (Box of 20) with potential pouch seal wrinkles that could breach sterility. Affected lots D180437A and D180567 may cause contamination during surgery. Return to Ecolab for replacement.
The pouches of certain lots of product may have wrinkles along the pouch seal that could result in a channel within the seal. Should there be a channel in the pouch seal it may result in a breach in the sterility of the product.
Ecolab is recalling Camera Arm Drapes sold in boxes of 20 that come sealed in poly-Tyvek pouches. The recall is because certain lots might have wrinkles in the pouch seal that could create a channel, risking a breach in the sterility of the product during medical procedures.
The pouches of certain lots may have wrinkles along the seal that create a channel. If this channel forms, it could allow contamination to breach the sterility of the product during surgery, potentially leading to infections.
Healthcare professionals using the Camera Arm Drapes for surgical procedures with the Da Vinci Si Robotic system are most at risk. The recall affects specific lots of the product sold to hospitals and medical facilities.
Check for the product name 'Camera Arm Drape (Box of 20)' sealed in poly-Tyvek pouches. Affected lots are D180437A and D180567, distributed by Intuitive Surgical for use with the Da Vinci Si Robotic system.
Look for lot numbers D180437A or D180567 on the pouch seal.
Contact Ecolab to return the affected product for a replacement.
The pouches of certain lots may have wrinkles that create a channel in the seal, risking a breach in sterility during medical procedures.
If the pouch seal has a channel, it could lead to contamination and infection during surgery, but the risk is low for most users.
Check for lot numbers D180437A or D180567 on the pouch seal of the Camera Arm Drape (Box of 20) sold for use with the Da Vinci Si Robotic system.
We’ve drafted a message you can send Ecolab to request your refund or repair — edit it as you like.
Subject: Recall Z-0232-2019 — Ecolab Ecolab Hello, I own a Ecolab that is covered by recall Z-0232-2019 from Ecolab. 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.
