Medline recalls specific Ethicon Harmonic ACE+7 Shears due to potential incomplete packaging seals. Affected units have unique item numbers and lot numbers. Consumers should check their product details to determine if recalled.
Potential for an incomplete seal on the packaging tray.
Medline is recalling certain Ethicon Harmonic ACE+7 shears that may have incomplete packaging seals. This could lead to improper handling or contamination if the seal fails. Affected items have specific item numbers and lot numbers listed in the recall.
The packaging seal might not close properly, potentially allowing contaminants to enter the shears. This could lead to improper sterilization or contamination if the seal fails during use. However, the risk is low as this is a packaging issue rather than a direct product failure.
Healthcare professionals using the specific Medline Ethicon Harmonic ACE+7 shears with the listed item numbers and lot numbers are most at risk. Patients and other users are less likely to be affected as these are medical devices used by professionals.
Check for item numbers HARH36R and lot numbers 499617, 499843, 500207, 500315, or 507265. The product is a 36cm Ethicon Harmonic ACE+7 shears with Advanced Hemostasis Use Only.
Verify your shears have item numbers HARH36R and lot numbers from the list provided in the recall.
The recall indicates a potential packaging seal issue, but the shears are generally safe. Affected units should be checked against the listed item numbers and lot numbers.
Check your shears against the item numbers and lot numbers listed in the recall. If they match, contact Medline for further instructions.
Look for item numbers HARH36R and lot numbers 499617, 499843, 500207, 500315, or 507265 on the packaging.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3095-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3095-2024 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.
