Medline recalls sterile procedural trays with potential for blades to puncture packaging foil. Affected units include specific lot numbers and item codes. Stop using immediately to prevent contamination.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling sterile procedural trays that could have blades puncturing the outer foil packaging. This risk might lead to contamination during medical procedures if the tray is used without proper sterilization.
Sterile blades inside the trays could puncture the outer foil layer of the packaging. This could allow contamination to reach the blades, making them unsafe for medical procedures.
Healthcare professionals and medical facilities using the recalled sterile procedural trays. Those handling the specific lot numbers and item codes are most at risk.
Check for item number DYNJ0185290G, case UDI/GT: 40193489378055, and unit UDI/GT: 10193489378054. The lot number 22HME772 is also associated with this recall.
Discard the recalled sterile procedural trays to prevent potential contamination during medical procedures.
Sterile blades inside the trays could puncture the outer foil layer of the packaging, risking contamination during medical procedures.
The affected items include the ANCILLARY PACK-LF. Sterile Procedural Tray with item number DYNJ0185290G, case UDI/GTIN 40193489378055, unit UDI/GTIN 10193489378054, and lot number 22HME772.
Check for the item number DYNJ0185290G, case UDI/GTIN 40193489378055, unit UDI/GTIN 10193489378054, and lot number 22HME772 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-1060-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1060-2023 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.
