Medtronic recalls specific percutaneous pin adapters used in StealthAir Frame Assembly. The adapter may rotate slightly after surgical placement and not return to original position, potentially causing complications.
Under certain circumstances, the percutaneous pin adapter used with the StealthAir Frame Assembly may slightly rotate after surgical placement and not return to its original position, even when connections are tight and secure.
Medtronic is recalling certain percutaneous pin adapters used with their StealthAir Frame Assembly. These adapters may rotate slightly after surgical placement and not return to their original position, which could lead to complications during medical procedures.
The percutaneous pin adapter may rotate slightly after surgical placement and not return to its original position, even when connections are tight and secure. This could potentially cause complications during medical procedures if the adapter shifts position.
Patients who received the specific percutaneous pin adapters with lot numbers listed in the recall are affected. Medical professionals using these adapters in surgical procedures are at risk.
Check the lot numbers on the adapter: 150114, 150505, 150506, 150904, 151005, 151007, 160201, 160224, 160419, 160617, 160707, 170216, 180110, and 180409. The adapters are part of specific kits including the Upgrade Set Percutaneous Pin and Medtronic Adapter Percutaneous Pin Kits.
Look for the lot numbers listed: 150114, 150505, 150506, 150904, 151005, 151007, 160201, 160224, 160419, 160617, 160707, 170216, 180110, and 180409.
Medtronic Adapter Percutaneous Pin, REF 9734752 (GTIN 00643169529489) and REF 9734752-G02 (GTIN 00763000054915).
Check the lot numbers on the adapter: 150114, 150505, 150506, 150904, 151005, 151007, 160201, 160224, 160419, 160617, 160707, 170216, 180110, and 180409.
The recall does not specify a remedy, so no action is required beyond checking the lot number.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0707-2020 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0707-2020 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.
