DeRoyal recalls specific ENDOVASCULAR TRACEPACK models due to potential injury from improper use. Affected units include Lot 56225516 through Lot 57754751. Consumers should check their product details and follow safety instructions.
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DeRoyal is recalling certain ENDOVASCULAR TRACEPACK products because they may cause injury if used incorrectly. This recall affects specific lot numbers with expiration dates up to January 2025. Consumers should stop using these products and contact DeRoyal for a replacement.
The hazard is not clearly described in the recall notice. Without specific details about how the product could cause injury, it's impossible to determine the exact risk mechanism.
Owners of DeRoyal ENDOVASCULAR TRACEPACK with lot numbers 56225516 through 57754751 are affected. Users who follow proper instructions are at low risk, but improper use could lead to injury.
Check the product's lot number on the packaging. Affected lots include 56225516 (exp 6/1/2024), 56395460 (exp 6/1/2024), 56620751 (exp 10/1/2024), 56780958 (exp 10/1/2024), 57190141 (exp 10/1/2024), and 57754751 (exp 1/1/2025).
Look for the lot number on the packaging to determine if your product is affected.
If your product is in the affected lot list, stop using it immediately to avoid potential injury.
DeRoyal ENDOVASCULAR TRACEPACK with lot numbers 56225516 through 57754751.
Check the lot number on the packaging; affected lots include 56225516 (exp 6/1/2024), 56395460 (exp 6/1/2024), 56620751 (exp 10/1/2024), 56780958 (exp 10/1/2024), 57190141 (exp 10/1/2024), and 57754751 (exp 1/1/2025).
Stop using the product immediately and contact DeRoyal for a replacement.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0649-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0649-2023 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.
