Medline recalls custom sterile procedural kits with Turkuaz ultrasound gel that may not meet sterility standards. Affected kits sold between April 2020 and April 2023 need to be checked for specific model numbers and UPCs.
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Medline is recalling certain custom sterile and non-sterile procedural kits that contain Turkuaz ultrasound gel. The gel might not meet sterility requirements, which could lead to infections during medical procedures.
The ultrasound gel in the kits may not meet sterility standards, meaning it could be contaminated. This contamination could lead to infections during medical procedures if the gel is used without proper sterilization.
Healthcare providers using these kits for fetal interventions or other procedures are most at risk. Patients undergoing procedures with these kits could face infection if the gel isn't sterile.
Check for model numbers DYNJ66041A/B, DYNJ62319A/B, DYNDV2397, DYNJ24276C, or DYNJ27275. These kits were sold by Medline between April 2020 and April 2023 with specific UPC numbers listed in the recall.
Look for model numbers DYNJ66041A, DYNJ66041B, DYNJ62319A, DYNJ62319B, DYNDV2397, DYNJ24276C, or DYNJ27275 on the kit packaging.
Check if the kit has the listed UPC numbers: 019348948028, 019532715107, 019348947486, 019348999548, 019348938846, 088438943118, or 008019683311.
The ultrasound gel in these kits may not meet sterility specifications, which could lead to infections during medical procedures.
Check the model number and UPC on the kit to see if it's affected. If it is, contact Medline for instructions.
The gel might not be sterile, which could cause infections during procedures. However, the recall is for specific kits and not all ultrasound gel products.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2332-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-2332-2023 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.
