Medline Custom procedural kits (GP-NEURO PACK, KIT NEUR FUS LUM POST, etc.) contain leaking isopropyl alcohol bottles. Affected kits have specific model numbers and lot codes. Consumers should stop using these kits immediately.
Kits contain leaking bottles of isopropyl alcohol
Medline Custom procedural kits with leaking isopropyl alcohol bottles are being recalled. This hazard poses a risk of skin irritation or other injuries from exposure to the alcohol. Affected kits have specific model numbers and lot codes listed in the recall.
The kits contain bottles of isopropyl alcohol that leak, potentially causing skin irritation or other injuries if exposed. Leaking alcohol can also lead to accidental contact with sensitive areas during medical procedures.
Healthcare professionals and medical facilities that use Medline Custom procedural kits are most at risk. The kits are designed for medical procedures and may be used in hospitals or clinics.
Check for the model numbers listed in the recall: DYNJ0397191V, DYKMBNDL138, DYNJ907374, etc. Also check the lot numbers provided for each model. These kits are sold under the Medline Custom procedural kit labels.
Discontinue use of all recalled Medline Custom procedural kits with leaking isopropyl alcohol bottles.
The affected kits include GP-NEURO PACK, KIT NEUR FUS LUM POST, KIT PEDI VP SHUNT, and others with model numbers like DYNJ0397191V, DYKMBNDL138, DYNJ907374, etc.
Check the model number and lot code on your kit. The recall lists specific model numbers and corresponding lot numbers for each kit type.
Stop using the kit immediately and contact Medline for further instructions. The recall does not specify a return process or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1476-2022 — Medline Medline Hello, I own a Medline that is covered by recall Z-1476-2022 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.
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.
