Main Street Law Firm is no longer accepting acid reflux drug cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting Allergan textured implant cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting Essure birth control cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting hip replacement cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting Camp Lejeune cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting Elmiron cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting JUUL and E-Cigarette cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
Main Street Law Firm is no longer accepting CPAP and BiPAP cases. If you feel that you may have a case, we urge you to contact another firm suited to handle your case.
The Main Street Law Firm is no longer taking new cases in this matter.
Other Military Cases:
If you or a loved one are a U.S. military service member, veteran, or military contractor who suffered injuries from certain explosive terrorist devices between 2003 and 2011, you may have a claim for significant damages without ever going to court and even if you are already receiving disability or other compensation.
Research has found evidence that links a common firefighting foam with the development of cancer in its users. Those that have been exposed to the dangerous chemicals by ingesting them orally, absorbing them through the skin, or inhaling them through the air are at risk of developing various types of cancer. If you are a veteran of a military base or a resident who lived near a military base and subsequently developed cancer from exposure to the firefighting foam, fill out our free case review to see if you are eligible for compensation without ever going to court.
Zimmer Biomet Spinal Fusion and Long Bone Stimulator Recall
The devices have been identified by the FDA under a Class I recall, the most serious type of recall reserved for products or devices that may cause serious injuries or death.
Device uses
Zimmer’s implantable bone growth and spinal fusion stimulators are used to help heal broken long bones in the arms and legs or bone following spinal fusion surgery. The stimulators are implanted during surgery, primarily in individuals who have a health condition or whose bodies have difficulty healing bone on its own.
Here are the Zimmer devices identified under the recall:
· SpF-XL Implantable Spinal Fusion Stimulator
· SpF PLUS-Mini Implantable Fusion Stimulator
· Osteogen Implantable Bone Growth Stimulator
All of the devices were manufactured between February 14, 2015 and April 11, 2017 and would’ve been distributed between April 29, 2015 and March 31, 2018. The number of devices recalled totals 1,360 units in the U.S.
About the recall
The devices were recalled due to a “lack of adequate validation and controls to ensure that final products were clean and free from bacteria and chemical residue,” according to the FDA.
Side effects caused by these inadequacies include infection, swelling around the spinal cord, damage to other organs, tissue death, the need for additional surgeries, impaired wound and bone healing, paralysis, or death.
If you or a loved one were implanted with any of these stimulators after spinal fusion surgery or to help heal long bones and have suffered a severe side effect, contact us today.
