What’s the Problem?
This FDA Recall began on Dec. 9, 2020, and affects:
- 3 oz. Regenecare HA Hydrogel — NDC # 66977-107-03 — lot number 41262 — date 2021-01.
Use of the recalled Regenecare may result in local skin infections, bloodstream infections, sepsis, difficulty breathing, low blood pressure, fast heart rate, mental confusion and potentially death, FDA said.
Mesquite, Texas-based MPM Medical issued the recall following 2 customer complaints of visible contamination, which was subsequently found to be B. cepecia.
Consumers who experienced any adverse reactions or quality problems with Regenecare should contact their healthcare provider immediately.
Consumers with additional questions regarding the recall can contact MPM Medical Monday through Friday between 7AM and 5PM CST.
Do I Have a Regenecare Class Action Lawsuit?
The Class Action Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Regenecare Lawsuits. We are handling individual litigation nationwide and currently accepting new injury and death cases in all 50 states.
If you or another loved one was injured by the side effects of Regenecare, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.