Natus Medical recalls cranial access kits with sterile surgical drapes that have adhesive liners hard to remove, risking product damage. Affected kits include specific part numbers and lot numbers.
Due to Cranial Access Kits containing recalled sterile surgical drapes. The sterile surgical drapes are being recalled due to the liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable.
Natus Medical is recalling cranial access kits because the sterile surgical drapes contain adhesive liners that are hard to remove without damaging the product. This could make the kit unusable for medical procedures.
The adhesive liner on the sterile surgical drapes is difficult to remove without damaging the product. This could render the kit unusable during medical procedures requiring precise intracranial access.
Healthcare professionals using the Natus Cranial Access Kit for intracranial procedures are most at risk. The recall affects kits sold with specific part numbers and lot numbers.
Check for part numbers HITH1, HITHNDRZR, or HITHLT with corresponding lot numbers 22GDB675, 22HDA557, or 22IDB724. The kits are designed for single-use medical procedures.
Identify the part number and lot number on the kit to confirm if it is affected.
The sterile surgical drapes in the kit have adhesive liners that are difficult to remove without damaging the product, which could render it unusable.
Part numbers HITH1 (lot 22GDB675), HITHNDRZR (lot 22HDA557), and HITHLT (lot 22IDB724) are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send Natus Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0735-2023 — Natus Medical Natus Medical Hello, I own a Natus Medical that is covered by recall Z-0735-2023 from Natus 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.
