Medline recalls sterile procedural trays labeled PAIN SERVICE PACK-LF and LOCAL BASIC due to potential blade puncture of packaging. Affected units include specific lot numbers and item codes.
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 'PAIN SERVICE PACK-LF' and 'LOCAL BASIC' because sterile blades inside the trays could puncture the outer foil packaging. This risk 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 leading to infections during medical procedures.
Healthcare professionals using these trays for medical procedures are most at risk. Patients receiving procedures with these trays could face contamination risks.
Check for trays labeled 'PAIN SERVICE PACK-LF' or 'LOCAL BASIC'. Affected units have specific lot numbers: 22HDC372 and 22HBQ831, 22HBO949.
Look for the labels 'PAIN SERVICE PACK-LF' or 'LOCAL BASIC' on the tray.
Reach out to Medline for guidance on next steps if you have the affected units.
Sterile blades inside the trays could puncture the outer foil packaging, risking contamination during medical procedures.
Check for the labels 'PAIN SERVICE PACK-LF' or 'LOCAL BASIC' and contact Medline for guidance.
Yes, affected units include lot numbers 22HDC372 and 22HBQ831, 22HBO949.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1063-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1063-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
