Medline recalls sterile procedural trays (CARDIAC CATH PACK-LF, ANGIOGRAPHY-NS-LF, EP BASIC SET UP) due to potential blade puncture of packaging foil. Affected units have specific lot numbers and item 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 during medical procedures if the packaging is compromised.
Sterile blades inside the trays may puncture the outer foil layer of the packaging. If the foil is compromised, the sterile contents could become contaminated, potentially leading to infections during medical procedures.
Healthcare professionals using these trays for medical procedures are most at risk. Patients undergoing surgery or procedures with these trays could be exposed to contamination.
Check for specific item numbers like DYNJ0368386D (CARDIAC CATH PACK-LF) or lot numbers such as 22IMD669. These trays were sold with specific packaging labels and were manufactured in batches with known lot numbers.
Look for item numbers like DYNJ0368386D or lot numbers such as 22IMD669 on the trays.
Reach out to Medline Industries for specific information about your product and instructions on how to return or replace it.
Affected trays include CARDIAC CATH PACK-LF, ANGIOGRAPHY-NS-LF, EP BASIC SET UP, IMPLANT PACK-LF, PORT PACEMAKER INSERTION PACK, OPEN HEART PACK, LAP BASIN TRAY, ANGIO ACCESS, and ANGIO.
Check for item numbers like DYNJ0368386D or lot numbers such as 22IMD669 on the packaging labels.
Contact Medline Industries for specific instructions on how to return or replace the affected trays.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1066-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1066-2023 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.
