MEDLINE recalls M1S0179 STRL Tape/Pen Packs with weak seals that could breach sterility. Product code P519582A, lot numbers 2023031590 and 2023070390. Stop using if seal fails.
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
MEDLINE is recalling its M1S0179 STRL Tape/Pen Packs due to a weak seal that might breach sterility. This could lead to contamination of medical supplies if the seal fails, which may not be detectable by all users.
The tape/pen packs have a weak seal that might break, allowing contamination of sterile medical supplies. This breach could happen without being noticed by users, potentially leading to infections or complications.
Healthcare professionals using these tape/pen packs for medical procedures are most at risk. Patients receiving procedures with contaminated supplies could be affected.
Check for product code P519582A with lot numbers 2023031590 or 2023070390. The packs are sold under MEDLINE brand with UDI/DI numbers 20193489111375 (case) and 10193489111378 (each).
Inspect the seal for any signs of weakness or damage before use.
The recall states the seal may be weak and could breach sterility, so it's not safe to use without checking the seal.
The recall does not specify a remedy, so check the seal for weakness and do not use if you find any issues.
Look for product code P519582A with lot numbers 2023031590 or 2023070390.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-1452-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-1452-2024 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.
