Medline recalls laparoscopic procedural trays that may have sterile blades causing packaging breaches. Affected items include specific lot numbers and model codes. Consumers should contact Medline for details.
Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
Medline is recalling lapar: non-sterile procedural trays labeled as laparoscopic that could have sterile blades inside. This risk might cause the sterile packaging to breach, potentially leading to contamination during medical procedures.
Sterile blades inside non-sterile trays may puncture the outer foil layer, breaking the sterile packaging. This could lead to contamination during medical procedures if the trays are used without proper sterilization.
Healthcare professionals using these trays in surgical settings are most at risk. Patients undergoing procedures with these trays could face contamination risks.
Check for trays labeled 'LAPAROSCOPIC' with item number DYNJ900415L. Lot numbers 22HBO658 or 22JBV699 are affected. These trays come in cases with specific UDI/GTIN codes.
Reach out to Medline Industries for specific details about your affected product and next steps.
The recall indicates a potential risk of packaging breach, so they should not be used until Medline provides instructions.
Sterile blades inside non-sterile trays could puncture the foil layer, causing contamination during medical procedures.
Look for lot numbers 22HBO658 or 22JBV699, item number DYNJ900415L, or UDI/GTIN codes 40195327029426 (case) and 10195327029425 (each).
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1030-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1030-2023 from Medline Industries. 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.
