Medtronic recalls specific percutaneous pins due to potential cross-pin issues that could cause improper fit or removal. Affected units have unique serial numbers and were sold in 2023.
Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.
Medtronic is recalling certain percutaneous surgical pins because they might not fit properly into tap caps or become too tight to remove. This could lead to complications during medical procedures if the pin isn't used correctly.
The pin may have a cross-pin that prevents it from fitting into the tap cap or makes it too tight to remove. This could cause improper use during medical procedures if the pin doesn't function as intended.
Surgical patients or medical professionals using the recalled pins for procedures. The risk is low as the pins are sterile and used in controlled medical settings.
Check for the serial numbers: 2023010549, 2023010551, 2023010840, 2023041134, 2023051137, 2023051138, 2023051139, 2023060368, 2023060369. These pins were sold by Medtronic in 2023.
Verify if your pin has one of the listed serial numbers: 2023010549, 2023010551, 2023010840, 2023041134, 2023051137, 2023051138, 2023051139, 2023060368, 2023060369.
The recall indicates a potential issue with fit or removal, but the pins are sterile and used in controlled medical settings. Always follow your healthcare provider's instructions.
Check for the specific serial numbers listed in the recall: 2023010549, 2023010551, 2023010840, 2023041134, 2023051137, 2023051138, 2023051139, 2023060368, 2023060369.
The recall does not specify a remedy, so contact Medtronic directly for guidance on next steps.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0698-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0698-2024 from Medtronic. 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.
