DeRoyal recalls specific Peripheral VAS Pack models due to safety concerns. Affected units have lot numbers expiring 6/1/2023, 1/1/2024, or 2/1/2024. No remedy details provided in official notice.
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DeRoyal is recalling certain Peripheral VAS Packs with specific lot numbers because of an unexplained safety hazard. This recall affects users who own these particular models, which could pose risks if not addressed.
The recall indicates a safety hazard, but the official notice does not specify the exact mechanism or risk level. Without clear details on the hazard, it's impossible to determine how the product could be dangerous.
Owners of DeRoyal Peripheral VAS Packs with lot numbers 56618811 (expires 6/1/2023), 56779017 (expires 1/1/2024), or 57148495 (expires 2/1/2024) are affected. Users who have these specific models should check if they are impacted.
Check your DeRoyal Peripheral VAS Pack for lot numbers 56618811 (expires 6/1/2023), 56779017 (expires 1/1/2024), or 57148495 (expires 2/1/2024). The product is identified by its model reference number 89-10530.03.
Look for the lot number on your DeRoyal Peripheral VAS Pack to see if it matches 56618811, 56779017, or 57148495.
The official recall notice does not specify the exact hazard. The hazard is listed as 'XXX' in the record, indicating it was not clearly described.
The recall does not provide a remedy or specific instructions to stop using the product. The hazard level is unknown, so immediate action is not required based on this notice.
Check the lot number on your product. Affected units have lot numbers 56618811 (expires 6/1/2023), 56779017 (expires 1/1/2024), or 57148495 (expires 2/1/2024).
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0689-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0689-2023 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.
