LeMaitre recalls aortic occlusion catheters due to incorrect size listed on packaging. This may cause improper use during medical procedures. Affected units include specific lot numbers.
incorrect device size being listed on the impacted device packaging
LeMaitre is recalling aortic occlusion catheters because the packaging lists the wrong size. This could lead to improper use during medical procedures if the wrong size is used.
The incorrect size listed on packaging could lead to using the wrong catheter size during medical procedures. This might cause improper use, potentially affecting patient safety.
Healthcare professionals using the catheter for medical procedures are most likely affected. Patients receiving the catheter as part of treatment may also be impacted.
Check for the lot number OLC1051 on the packaging. The catheter comes in two sizes: 28 mm or 45 mm.
Look for the lot number OLC1051 on the packaging to confirm if the catheter is affected.
The catheter is offered in two sizes: 28 mm or 45 mm.
The recall is due to incorrect size listed on packaging, not a direct hazard causing injury. The risk is low.
Check for the lot number OLC1051 on the packaging.
We’ve drafted a message you can send LeMaitre to request your refund or repair — edit it as you like.
Subject: Recall Z-2448-2019 — LeMaitre LeMaitre Hello, I own a LeMaitre that is covered by recall Z-2448-2019 from LeMaitre. 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.
