Medline convenience kits labeled as MAJOR VASCULAR CDS, POST OP KIT, and others contain leaking isopropyl alcohol bottles. Recalled due to risk of spills and potential fire hazards.
Kits contain leaking bottles of isopropyl alcohol
Medline convenience kits with leaking isopropyl alcohol bottles are being recalled. These kits can cause spills or fires if the alcohol bottles leak, especially in medical settings.
The kits contain bottles of isopropyl alcohol that can leak, leading to spills. If spilled on flammable surfaces, this could cause a fire. Healthcare settings have many flammable materials, increasing the risk.
Healthcare professionals and medical facilities using the recalled Medline convenience kits are most at risk due to potential spills and fire hazards from leaking alcohol bottles.
Check for kits labeled as MAJOR VASCULAR CDS, POST OP KIT, KIT NEURO FUS LUM POST SANSUR, or other specific names listed in the recall. Look for model numbers like CDS981543D, DYKM1875, or others with the listed lot numbers.
Immediately stop using any Medline convenience kits that contain leaking isopropyl alcohol bottles, as they pose a fire risk.
Kits labeled as MAJOR VASCULAR CDS, POST OP KIT, KIT NEURO FUS LUM POST SANSUR, PRE-OP ACCESSORY KIT CHOICE, DEEP BRAIN STIMULATION PACK, MINIMALLY INVASIVE PACK-LF, EVLP Pack/Kit, GENERAL PURPOSE CV, KIT GERMANTOWN CABG, and DENTAL RESTORATIONS with the listed model numbers and lot numbers.
Check the model number and lot number on your kit against the list provided in the recall notice, which includes specific model numbers like CDS981543D and lot numbers such as 19HBK745.
Immediately stop using the kit and contact Medline for instructions on how to safely dispose of or return the kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1474-2022 — Medline Medline Hello, I own a Medline that is covered by recall Z-1474-2022 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.
