DeRoyal recalls specific MAJOR ORTHO PACK models due to potential injury from improper use. Affected units include Lot 56388551 (exp 10/1/2024) and Lot 56780333 (exp 3/1/2025).
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DeRoyal is recalling specific MAJOR ORTHO PACK models because they can cause injury if used incorrectly. This recall affects certain lot numbers with expiration dates listed in the record.
The recall indicates a potential injury risk from improper use, but the exact hazard mechanism is not described in the record. Without specific details on how the product could cause harm, the risk cannot be fully assessed.
Users of the DeRoyal MAJOR ORTHO PACK with the specified lot numbers are affected. Individuals who have the product and use it improperly are at risk.
Check the product label for the lot numbers: 56388551 (expires 10/1/2024) or 56780333 (expires 3/1/2025). The product is the DeRoyal MAJOR ORTHO PACK with reference number 89-9250.07.
Look for lot numbers 56388551 (expires 10/1/2024) or 56780333 (expires 3/1/2025) on the DeRoyal MAJOR ORTHO PACK.
The recalled product is the DeRoyal MAJOR ORTHO PACK with reference number 89-9250.07.
Lot numbers 56388551 (expires 10/1/2024) and 56780333 (expires 3/1/2025) are affected.
The recall record does not specify a remedy, so no action is required beyond checking the product label for 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-0637-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0637-2023 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.
