Cartiva Toe Implant Litigation is Centralized

Recently, plaintiffs in five lawsuits moved under 28 U.S.C. section 1407 to centralize litigation about Cartiva toe implants in the District of Maryland or the Northern District of Illinois. 🗃📄💼

The Judicial Panel determined that the five lawsuits involved common questions of fact and that centralization in the Eastern District of Arkansas would serve the parties’ and witness’ convenience, promoting just and efficient actions in the litigation.

If you were harmed by Cartiva toe implants, you should contact the lawyers of Moll Law Group a call to determine whether you have a viable claim.

4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death

The Consumer Product Safety Commission has become aware of a minimum of 150 cases where consumers reported that the plastic tip restraint kits broke on 4our Kiddies tip restraint kits which were sold on Amazon.com. ‼️😱

If you or your child was injured as a result of a tip-over or entrapment caused by 4our Kiddies tip restraint kits, contact Moll Law Group.

The Food and Drug Administration Warns Liver Injuries Possible

The FDA has announced that it discovered cases of liver injury among patients taking Amgen’s drug for a group of rare autoimmune diseases. The FDA asked healthcare providers to stop using this treatment if there’s a suspicion of organ injury or damage. 🛑💊

If you were injured as a result of taking the Amgen drug—Tavneos—you should consult the seasoned Chicago-based lawyers of Moll Law Group.

Certain Abbott Glucose Monitors Are Recalled

Internal testing at the manufacturer determined that certain sensors can offer incorrect readings of low glucose. The consequences of this may involve injuries, complications, or even death. This is a Class I Recall, the most serious type of recall.

The FDA has reported that, based on medical device maker Abbott Laboratory’s company data, there have been 860 serious injuries connected to the recall of certain glucose monitoring sensors.

If you were harmed by one of the FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors, you should call the product liability lawyers of Moll Law Group. Read more here.

AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall

Hazard; Violates Mandatory Standard for Bedside Sleepers

Recently, AirClub convertible bassinets were recalled because of the risk of severe injury or death as a result of falls. 🙅🛏The bassinets were found to violate the mandatory standard for bedside sleepers because the mechanism that attaches the bassinet to an adult’s bed leaves a space between the bedside sleeper and mattress. An infant could fall through that space.

If your infant was injured as a result of an AirClub convertible bassinet, you should consult the seasoned product liability lawyers of Moll Law Group. Billions have been recovered in lawsuits with which we’ve been involved.