Medline recalls 100+ probe cover kits with sterile ultrasound gel due to potential inadequate seam barriers. These kits were sold from Dec 2017-May 2023. Check model numbers listed for affected items.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling probe cover kits that contain sterile ultrasound gel. The covers may have an inadequate barrier at the seams, which could lead to contamination during medical procedures. This affects specific model numbers sold between December 2017 and May 2023.
The probe covers may have an inadequate barrier at the seams, potentially allowing contaminants to enter the ultrasound gel during medical procedures. This could lead to infection or contamination risks for patients and healthcare workers.
Healthcare professionals using these kits for diagnostic ultrasound procedures are most at risk. Patients receiving procedures with these kits could be exposed to contamination.
Check the model number on the kit. Affected models include CRANIOTOMY CDS-1 (CDS982889I), JOINT INJECTION TRAY (DYNDH1722), and others listed in the recall notice. These kits were distributed between December 2017 and May 2023.
Look for model numbers like CDS982889I, DYNDH1722, or DYNJ0604434X on the kit packaging.
The probe covers may have an inadequate barrier at the seams, potentially allowing contaminants to enter the ultrasound gel during medical procedures.
Affected models include CRANIOTOMY CDS-1 (CDS982889I), JOINT INJECTION TRAY (DYNDH1722), LOWER EXTREMITY PACK-LF (DYNJ0604434X), and others listed in the recall notice.
These kits were distributed from December 2017 to May 2023.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2191-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2191-2023 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.
