Synvisc One Recall Number

In December 2017, Sanofi Genzyme voluntarily recalled Synvisc-One, as a result of microbial contamination of lot number 7RSL021 sold in 36 U.S. states from October 25, 2017, through November 7, 2017. This recalled lot equates to 12,380 syringes. On February 14, 2018, nearly two months after the manufacturer initiated the recall, the recall was updated. The company revealed that the bacterial contaminant in the syringes was Methylbacterium thiocyanatum.

However, Sanofi Genzyme did not express which side effects prompted the recall. A representative of the pharmaceutical company stated the infected syringes increased the presence of side effects found on the label.  The warnings listed on the package insert include pain, swelling, heat, redness, and fluid build-up in and around the knee.

Synvisc One Recall Number

Sanofi Genzyme has not been forthcoming to consumers about the specifics of the recall. In fact, the company has given many the runaround when calling the pharmaceutical company to any information. This is why if you are concerned that your osteoarthritis medication was contaminated to call the Synvisc One recall number at 1-877-513-9517. We have over 20 years of experience representing injured consumers and giving them knowledge and justice.

Seek Justice

Many people after receiving the contaminated syringes from lot number 7RSL021 sold in 36 U.S. states from October 25, 2017, through November 7, 2017, are still in pain today, months later. They are still in excruciating pain after being infected by an antibiotic-resistant bacteria and Sanofi Genzyme is responsible. We are determined to ensure they give compensation to those affected by this Synvisc-One bacteria.

Therefore, if you or someone you love received the Synvisc-One from the contaminated lot distributed between October and November 2017 and experienced a painful side effect, contact us today for a free, no obligation case review. The Synvisc One recall number is 1-877-513-9517.

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