DeRoyal recalls LAPINECTOMY PACK model REF 89-7198.10 due to risk of serious injury. Affected units have specific lot numbers expiring July 2026.
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DeRoyal is recalling LAPINECTOMY PACKs with specific lot numbers because they pose a risk of serious injury. This recall affects medical devices used in certain procedures.
The recall states the product is unsafe but does not specify the exact hazard mechanism. Without clear details on how the product could cause harm, the risk cannot be fully assessed.
Medical professionals who use DeRoyal LAPINECTOMY PACKs for surgical procedures are most at risk. Patients receiving these packs during surgery may also be affected.
Check for lot numbers 56612971 or 56802580 on the packaging, which expire on July 1, 2026. These units were sold with the reference number REF 89-7198.10.
Look for lot numbers 56612971 or 56802580 on the packaging of the DeRoyal LAPINECTOMY PACK.
The recall states the product is unsafe but does not specify the exact hazard mechanism.
Check for lot numbers 56612971 or 56802580 on the packaging, which expire on July 1, 2026.
The recall does not specify a remedy, so no action is required beyond checking the lot number.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0588-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0588-2023 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.
