Medline recalls sterile procedural trays for breast biopsy that may have blades puncturing packaging foil. Affected items include specific model numbers and lot numbers. Consumers should contact Medline for details.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling sterile procedural trays used for breast biopsies because the blades inside could puncture the outer foil packaging. This risk could lead to contamination if the packaging is compromised during use.
The sterile blades inside the trays could puncture the outer foil layer of the packaging. If the packaging is compromised, it might lead to contamination during medical procedures.
Healthcare professionals and patients using Medline's sterile procedural trays for breast biopsies. Those with the specific model numbers and lot numbers listed are most at risk.
Check for model numbers DYNJS3035 (for MINOR/BREAST BIOPSY-LF) or DYNJT1911D (for BREAST BIOPSY-LF). Look for lot numbers 22IBK248, 22IBB171, 22HBM446 or 22JBG862, 22HBV267.
Review the model number and lot number on the tray packaging to confirm if it matches the recalled items.
The sterile blades inside the trays have the potential to puncture the outer foil layer of the packaging, which could lead to contamination during medical procedures.
Check for model numbers DYNJS3035 (MINOR/BREAST BIOPSY-LF) or DYNJT1911D (BREAST BIOPSY-LF) and lot numbers 22IBK248, 22IBB171, 22HBM446 or 22JBG862, 22HBV267.
The recall record does not specify a remedy, so contact Medline directly for instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1073-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1073-2023 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.
