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Why Was the Device Recalled?
Some LINX devices had defects that caused the beads to separate or migrate. This can result in:
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Recurring GERD symptoms
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Difficulty swallowing
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Bloating or chest pain
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Device migration or injury to the esophagus
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Need for revision or removal surgery
The FDA issued the recall to protect patients who had these devices implanted.
Who May Qualify for a LINX Lawsuit?
You may have a claim if you:
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Had a LINX device implanted
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Experienced complications such as device migration, separation, or failure
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Required revision or removal surgery
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Suffered other health problems caused by the device
Our attorneys have experience holding manufacturers accountable for defective medical devices.


Our Values

Values That Drive Us
01
Unwavering Integrity
02
Client-Centered Advocacy
03
Commitment to Justice
04
Empathy
05
Compassion

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