MicroAire recalls SmartRelease Endoscopic Carpal Tunnel Release Handpieces with part numbers 81014 and 83014 due to a higher than normal incidence of the blade not retracting when tightening.
There was a higher than normal incidence rate of the blade not retracting when tightening.
MicroAire is recalling SmartRelease Endoscopic Carpal Tunnel Release Handpieces (ECTR handpieces) with specific part numbers because the blade may not retract properly when tightening. This could lead to improper surgical procedures or injury if the blade remains in place during use.
The blade may not retract when tightening, which could cause it to stay in place during surgery. This might lead to improper tissue cutting or injury if the blade is not properly secured.
Surgical professionals who use MicroAire SmartRelease ECTR handpieces with part numbers 81014 or 83014 are likely affected. Surgeons performing carpal tunnel release procedures are at the highest risk.
Check if your handpiece has part numbers 81014 or 83014. Serial numbers listed in the recall include a range from 13388 to 13516.
Look for part numbers 81014 or 83014 on the handpiece.
Reach out to MicroAire Surgical Instruments for further assistance if you have the recalled part numbers.
The recall is due to a higher than normal incidence of the blade not retracting when tightening, which could lead to improper surgical procedures.
Part numbers 81014 and 83014 are affected, with serial numbers ranging from 13388 to 13516.
The recall does not require immediate discontinuation; however, you should check if your handpiece has the affected part numbers.
We’ve drafted a message you can send MicroAire to request your refund or repair — edit it as you like.
Subject: Recall Z-2222-2019 — MicroAire MicroAire Hello, I own a MicroAire that is covered by recall Z-2222-2019 from MicroAire. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
