Medline recalls sterile procedural trays with potential for blades to puncture outer foil packaging. Affected items include ST. ANNE'S MAJOR BASIN SET UP and other basin sets sold with specific lot numbers.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling certain sterile procedural trays that could have blades puncturing the outer foil packaging. This risk could lead to contamination or injury during medical procedures if the packaging is compromised.
Sterile blades inside the trays could puncture the outer foil layer of the packaging. This might cause contamination or injury if the packaging is compromised during medical procedures.
Healthcare professionals using these trays in medical settings are most at risk. Patients and staff handling the trays during procedures may be affected if the packaging is punctured.
Check for specific product names like ST. ANNE'S MAJOR BASIN SET UP, SINGLE BASIN SET, or DOUBLE BASIN SET. Look for lot numbers 22JLA323, 22ILA590, 22JBW819, 22IBK206, and others listed in the recall notice.
Look for the product name and lot number on the packaging to determine if it's affected.
The recall includes trays labeled ST. ANNE'S MAJOR BASIN SET UP, SINGLE BASIN SET, DOUBLE BASIN SET, and other basin sets with specific lot numbers listed in the notice.
Check the product name and lot number on the packaging. Affected items have lot numbers like 22JLA323, 22ILA590, 22JBW819, 22IBK206, and others listed in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance on handling affected items.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1078-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1078-2023 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.
