Aerolase Corporation recalls LightPod ERA lasers due to missing remote interlock connector, which could cause injury during use. Affected units sold in the U.S. from 2020 onward.
This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device
Aerolase Corporation is recalling LightPod ERA lasers because they lack a required remote interlock connector. This could lead to injury if the laser is used without the safety feature.
The laser requires a remote interlock connector to prevent accidental activation. Without this connector, the device could activate unexpectedly during use, potentially causing injury.
Users of LightPod ERA lasers in the U.S. who purchased the device from 2020 onward are affected. Individuals using the laser for medical procedures are at higher risk.
Check for LightPod ERA lasers with the model name listed as 'LightPod ERA Lasers'. The recall applies to units sold in the U.S. starting in 2020.
Verify if your LightPod ERA laser has a remote interlock connector. If it does not, it is affected.
The laser lacks a required remote interlock connector, which could cause injury if the device activates unexpectedly during use.
The recall record does not specify a remedy or fix for the missing connector.
LightPod ERA lasers were sold in the U.S. starting in 2020.
We’ve drafted a message you can send Aerol:se to request your refund or repair — edit it as you like.
Subject: Recall Z-0768-2020 — Aerol:se Aerol:se Hello, I own a Aerol:se that is covered by recall Z-0768-2020 from Aerol:se. 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.