DeRoyal Industries recalls breast augmentation packs with specific lot numbers due to potential injury risk. Consumers should check their product details and follow safety instructions.
XXX
DeRoyal Industries is recalling breast augmentation packs with certain lot numbers because they may pose a risk of injury. This recall affects individuals who own these specific packs and requires them to take action to ensure safety.
The recall indicates a potential risk of injury, but the specific hazard mechanism is not clearly described in the record. Without details on how the product could cause harm, the exact danger cannot be determined.
Individuals who purchased the DeRoyal breast augmentation packs with lot numbers 55968916, 56620786, or 56780667 expiring July 1, 2023, are affected. Those using these products are at risk if they do not take action.
Check your DeRoyal breast augmentation pack for lot numbers 55968916, 56620786, or 56780667 that expire on July 1, 2023. These specific lots are part of the recall.
Identify your DeRoyal breast augmentation pack's lot number and expiration date to see if it matches the recalled lots.
The recall record states a potential risk of injury but does not specify the exact hazard mechanism.
The recall record does not provide a remedy or specific action steps beyond checking product details.
Check your DeRoyal breast augmentation pack for lot numbers 55968916, 56620786, or 56780667 expiring July 1, 2023.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0663-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0663-2023 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.
