Medline recalls specific sterile surgical blades due to potential puncture of outer foil packaging, risking contamination. Affected items include CISION10CS through CISION21SS with listed lot numbers. Consumers should check their product labels and contact Medline for details.
Potential of the blade puncturing the outer foil layer causing a breach in the sterile packaging.
Medline is recalling certain sterile surgical blades that could puncture the outer foil packaging, potentially causing contamination. This recall affects specific models and lot numbers used in surgical procedures.
The blades could puncture the outer foil layer of the sterile packaging, creating a breach that might allow contamination. This risk is specific to the packaging integrity during use in surgical procedures.
Healthcare professionals and surgical staff who use these specific Medline CISION sterile blades are most at risk. Patients using the recalled blades during procedures may face contamination risks.
Check for the product labels with item numbers CISION10CS through CISION21SS. Look for the corresponding lot numbers listed in the recall notice for affected items.
Look for the item number on the blade packaging, such as CISION10CS or CISION21SS.
Reach out to Medline Industries for specific instructions on how to handle recalled items.
The recall includes specific sterile surgical blades with item numbers CISION10CS through CISION21SS, each with associated lot numbers.
Check the item number on the blade packaging and compare it to the list of affected item numbers (CISSION10CS through CISION21SS) and lot numbers provided in the recall notice.
The recall does not require immediate discontinuation; healthcare professionals should check their product labels and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0930-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-0930-2023 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.
