Medline recalls surgical kits containing Codman Disposable Perforators 14mm with inadequate welds that may break or separate during use.
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 surgical kits that include Codman Disposable Perforators 14mm due to inadequate welds. These perforators may break or separate, which could lead to complications during medical procedures.
The perforators have inadequate welds on specific lots, meaning they may break or separate during use. This could cause injury or complications during surgical procedures if the perforator fails unexpectedly.
Surgical professionals using Medline kits with specific SKUs and kit lots listed in the recall. Patients undergoing procedures with these kits are at risk of complications if the perforators break.
Check for the following SKUs and kit lots: CRANI ADD A PACK (SKU DYNJ30926O), CRANIOTOMY (SKU CDS983611N), CRANIOTOMY CDS (SKU CDS983467J), CRANIOTOMY PACK (SKUs DYNJ85807A and DYNJ85927), and MAJOR CRANIOTOMY PACK (SKU DYNJ82007A). The kit lots include specific combinations like 24AMF811, 23KBA720, 23LBI611, and others listed in the recall.
Look for kit lot numbers on the packaging, such as 24AMF811 or 23KBA720, to determine if your kit is affected.
Reach out to Medline directly using the contact information provided in the recall notice to confirm if your specific kit is affected.
The recall is due to inadequate welds on specific lots of Codman Disposable Perforators 14mm, which may cause them to break or separate during use.
Check the kit lot numbers on the packaging to see if it matches the affected lots listed in the recall. If affected, contact Medline for further instructions.
Yes, if the perforators break or separate during surgery, it could lead to complications for patients.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1809-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1809-2025 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.
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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.
