Medline Industries recalls Centurion procedure kits with specific pack numbers due to potential leaks and breakage that could harm patients during medical procedures.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline Industries is recalling several Centurion procedure kits that contain plastic syringes prone to leaks and breakage. This could pose a risk to patient health during medical procedures.
The plastic syringes in these kits can leak or break, potentially causing contamination or injury to patients during medical procedures. This risk is related to the quality issues identified by the FDA Safety Alert.
Healthcare providers using these kits for procedures like bone marrow extraction or biopsies are most at risk. Patients undergoing procedures with these kits may face health issues.
Check for Centurion procedure kits labeled with specific pack numbers: BONE MARROW TRAY (SPEC0255), CT/ULTRASOUND BIOPSY (SPEC0262), FINE LACERATION KIT (SUT17215), INFECTION DRIVELINE MANAGEMENT KIT (DM645), LACERATION TRAY (DYNDL1159B), or SUTURE TRAY (DYNDS1064B).
Look for specific pack numbers on the kit labels to determine if it is recalled.
The FDA Safety Alert issued on March 19, 2024 identified leaks and breakage issues in the plastic syringes that could pose a risk to patient health.
The recall record does not specify a remedy, so check with Medline Industries for further instructions.
Yes, avoid kits with pack numbers SPEC0255 (Lot 2020042080), SPEC0262 (Lot 2018111280), SUT17215 (Lot 2020042080), DM645 (Lots 2018111280 and 2020042080), DYNDL1159B (Lot 2018111280), and DYNDS1064B (Lot 2020042080).
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-2770-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-2770-2024 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.
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.
