DeRoyal recalls Cataract Pack CSM with specific lot numbers due to potential injury from 3M Health Care Steri Drapes. Affected items contain recalled drapes that may cause harm.
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
DeRoyal is recalling specific Cataract Pack CSM products that include 3M Health Care Steri Drapes with certain lot numbers. These drapes could cause injury if used improperly.
The recalled Steri Drapes from 3M Health Care may not be properly secured during use, leading to potential injury. The hazard is not clearly described in the recall notice as to how it causes harm.
Patients and medical professionals who use DeRoyal Cataract Pack CSM products with the listed lot numbers are affected. Those handling the recalled drapes during eye surgery are at higher risk.
Check the lot number on the DeRoyal Cataract Pack CSM product. The affected lots are 55807995 (expires 1/1/2023), 56029890, 57001098, 57198118, and 56613261.
Identify the lot number on your DeRoyal Cataract Pack CSM product to see if it matches the affected lots listed.
The recall does not specify the exact hazard mechanism, so the official notice does not state how these drapes could cause injury.
Check the lot number on your DeRoyal Cataract Pack CSM product. Affected lots are 55807995 (expires 1/1/2023), 56029890, 57001098, 57198118, and 56613261.
The recall does not specify a stop-use instruction, so the official notice does not state that you should stop using the products.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0580-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0580-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.