Medline recalls sterile procedural trays (PELVISCOPY PACK and D-PELVISCOPY) due to risk of sterile blades puncturing 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 sterile procedural trays labeled PELVISCOPY PACK and D-PELVISCOPY because sterile blades inside the trays could puncture the outer foil packaging. This could lead to contamination of the sterile items during medical procedures.
Sterile blades inside the trays may puncture the outer foil layer of the packaging. This could allow contaminants to enter the sterile items, potentially causing infections during medical procedures.
Healthcare professionals using these trays for surgical procedures are most at risk. Patients receiving procedures using these trays could be exposed to contamination.
Check for item numbers DYNJ82555 (PELVISCOPY PACK) or DYNJ900628I (D-PELVISCOPY). Lot numbers 22HBQ035 or 22JDB340 are also indicators of affected units.
Identify the item number and lot number on the packaging to confirm if your tray is affected.
Sterile blades inside the trays have the potential to puncture the outer foil layer of the sterile packaging, which could lead to contamination during medical procedures.
Affected trays have item numbers DYNJ82555 (PELVISCOPY PACK) or DYNJ900628I (D-PELVISCOPY) and lot numbers 22HBQ035 or 22JDB340.
Check the item number and lot number on the packaging to confirm if your tray is affected. If it is, 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-1090-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1090-2023 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.
