Medline recalls Carrollton Hip FX Convenience kits (SKU SYNJ910:003A) due to potential packaging seal gaps that could allow contaminants to enter during use. Affected kits were sold with specific lot numbers and UDI-DI codes.
Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
Medline is recalling Carrollton Hip FX Convenience kits used in surgical procedures because a packaging error may create a seal gap. This gap could let contaminants enter the kit, potentially causing infection or other issues during surgery. The recall affects kits with specific lot numbers and UDI-DI codes.
An incomplete seal in the packaging can create a gap that allows contaminants to enter the kit. This could lead to infections or other complications during surgical procedures if the kit is used without proper sterility.
Healthcare professionals using the Carrollton Hip FX Convenience kits for surgical procedures are likely affected. The risk is highest for those handling the kits in sterile environments where contamination could occur.
Check for the SKU SYNJ910003A, UDI-DI code 10889942848447, and lot number 24EBP466 on the packaging. These kits were sold by Medline in Northfield, Illinois.
Inspect the packaging for an incomplete seal that may create a gap.
The recall is due to a packaging error that may create a seal gap, allowing contaminants to enter the kit during use.
The official notice does not specify a remedy or action for affected kits.
Check for SKU SYNJ910003A, UDI-DI code 10889942848447, and lot number 24EBP466 on the packaging.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0349-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0349-2025 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.
