Medline recalls breast biopsy and ultrasound biopsy probe cover kits with potential inadequate barrier at seams. These kits contain sterile ultrasound gel and were sold from December 2017 to May 2023.
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Medline is recalling several probe cover kits used in breast and soft tissue biopsies. These kits may have an inadequate barrier at the seams, which could lead to contamination during ultrasound procedures. If you own any of these kits, stop using them immediately.
The probe covers may have an inadequate barrier at the seams, which could allow contaminants to enter the sterile ultrasound gel during procedures. This might lead to infection or contamination of the patient's tissues.
Healthcare professionals and medical facilities that use Medline's probe cover kits for breast and soft tissue biopsies. Those who have the specific model numbers listed in the recall are most at risk.
Check for model numbers listed in the recall: DYNDA1224B, DYNDH1121C, DYNDH1124, and other specific model numbers from December 2017 to May 2023. All lots within expiry dates are affected.
Discontinue use of all recalled Medline probe cover kits to prevent potential contamination during ultrasound procedures.
The recall includes model numbers such as DYNDA1224B, DYNDH1121C, DYNDH1124, and others listed in the record from December 2017 to May 2023.
Check the model number on your kit. Affected models are listed in the recall from December 2017 to May 2023, including specific model numbers like DYNDA1224B and DYNDH1121C.
The recall record does not mention any replacement or repair options. Affected kits must be stopped from use immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2170-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2170-2023 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.
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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.
