Medline recalls specific kits containing Codman Disposable Perforators with inadequate welds that may break or separate. Affected kits include CRANI ACCESSORY PACK and CRANI PACK-LF models. Stop using immediately.
Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
Medline is recalling kits that contain Codman Disposable Perforators with inadequate welds. These perforators may break or separate during use, which could lead to injury if they become detached.
The perforators have inadequate welds on specific lots, which can cause them to break or separate during use. If the perforator breaks, it may become a sharp object that could cause injury to the user or patient.
Healthcare professionals using Medline kits with the specified Codman Perforators are affected. Surgeons and medical staff who have purchased the recalled kits are most at risk.
Check if your Medline kit includes the CRANI ACCESSORY PACK SKU DYNJ59270 or CRANI PACK-LF SKU DYNJ44805M. The kits also include specific SKUs listed in the recall notice with associated lot numbers.
Discontinue use of all recalled Medline kits containing the affected Codman Perforators to prevent potential injury.
The recall affects Medline kits with specific SKUs including CRANI ACCESSORY PACK SKU DYNJ59270 and CRANI PACK-LF SKU DYNJ44805M, as listed in the recall notice.
Immediately stop using the kits and contact Medline for instructions on returning or discarding the affected items.
Yes, perforators with inadequate welds may break or separate, which could cause injury if they become detached during use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1811-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1811-2025 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.
