DeRoyal recalls OPEN SHOULDER PROCEDURE PACK RF with affected 3M Health Care Steri Drapes due to potential safety issues. 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 OPEN SHOULDER PROCEDURE PACK RF products that contain specific 3M Health Care Steri Drapes. These drapes were manufactured with a batch that has a safety issue, so they need to be stopped from use to prevent potential harm.
The recall involves 3M Health Care Steri Drapes that were manufactured with a batch that has a safety issue. The exact nature of the issue is not clearly described in the recall notice, so the potential risk is unknown.
Healthcare professionals using DeRoyal OPEN SHOULDER PROCEDURE PACK RF products with the affected Steri Drapes are likely affected. Those who have the specific lot numbers listed in the recall are at the highest risk.
Check your DeRoyal OPEN SHOULDER PROCEDURE PACK RF product for lot numbers 57391516 (expires 11/1/2024) or 57749549 (expires 8/1/2024).
Look for lot numbers 57391516 (expires 11/1/2024) or 57749549 (expires 8/1/2024) on the DeRoyal OPEN SHOULDER PROCEDURE PACK RF.
DeRoyal OPEN SHOULDER PROCEDURE PACK RF with lot numbers 57391516 (expires 11/1/2024) or 57749549 (expires 8/1/2024).
The recall involves 3M Health Care Steri Drapes that were manufactured with a batch that has a safety issue, but the exact risk is not clearly described in the notice.
The recall notice does not specify a remedy, so you should check the product lot number and contact DeRoyal if you have the affected lot numbers.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0575-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0575-2023 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.
