DeRoyal recalls spinal fusion packs with affected 3M Steri Drapes due to potential injury risk. Learn if your product is affected and what to do.
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
DeRoyal is recalling spinal fusion packs that contain specific 3M Steri Drapes. These drapes could pose a risk of injury if used improperly.
The recalled Steri Drapes contain a defect that could lead to injury during medical procedures. The exact mechanism isn't specified in the recall notice.
Medical professionals using spinal fusion packs with the affected Steri Drapes are most at risk. Patients receiving these procedures may also be affected.
Check for spinal fusion packs with model number REF 89-7515.12. Lot numbers 56254211 (expires 6/1/2026) or 56841212 (expires 9/1/2026) are affected.
Identify your spinal fusion pack model and lot numbers to confirm if it's affected.
The recall notice does not specify if the drapes are safe to use; they are being recalled due to potential injury risk.
The recall notice does not provide a remedy or action steps for affected products.
Check for spinal fusion packs with model number REF 89-7515.12 and lot numbers 56254211 (expires 6/1/2026) or 56841212 (expires 9/1/2026).
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0596-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0596-2023 from DeRoyal. 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.
