Medline medical procedure kits with specific model numbers and lot codes may have slight dimensional variations causing difficulty fitting into outer canisters. Consumers should check their product labels for the listed model numbers and lot codes.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline medical procedure kits for major and minor breast procedures were recalled due to a slight dimensional variation that could make them harder to fit into outer canisters. This issue doesn't pose a safety risk but may cause inconvenience during use.
The kits have a slight dimensional variation that can make them harder to fit into the outer canister. This issue is not a safety hazard but could cause minor inconvenience during medical procedures.
Medical professionals using Medline breast procedure kits with the specific model numbers and lot codes listed in the recall notice are affected. Patients using these kits may be at risk of difficulty during procedures.
Check your Medline procedure kit for the model numbers: MAJOR BREAST (DYNJ905004C) or MINOR BREAST (DYNJ905002B). Also, look for the lot numbers listed in the recall notice.
Look for the model numbers and lot codes on your Medline procedure kit to determine if it is affected.
The recall is due to a slight dimensional variation that may cause difficulty fitting into the outer canister, which is not a safety hazard but could cause minor inconvenience.
Affected models include MAJOR BREAST (DYNJ905004C) and MINOR BREAST (DYNJ905002B) with specific lot numbers listed in the recall notice.
No, the recall does not require stopping use; the issue is minor and does not pose a safety risk.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2707-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2707-2024 from Medline. 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.
