RecallHawk

Summary

CPSC recalled Evrysdi™ (risdiplam) by Genentech, a member of the Roche Group, of South San Francisco, Calif.. Hazard: The bottles containing the prescription drug can leak due to a fit issue between the press-in bottle adapter and bottleneck. If the bottle is leaking, there is a risk of drug exposure by contact with skin or eyes. Prescription drugs must be in child resistant packaging that prevents children from gaining access to the contents as required by the Poison Prevention Packaging Act (PPPA).. Remedy: Consumers should immediately store Evrysdi in a safe location out of reach and sight of children. Consumers should inspect the bottle for any leaking. If it is leaking, contact Genentech for a free replacement. Consumers can continue to use as directed, as the leakage is not anticipated to impact the safety or efficacy of administered medicine. If Evrysdi gets on your skin, wash the area with soap and water. If Evrysdi gets in your eyes, rinse your eyes with water. Genentech is contacting all known purchasers directly..

Details

Source

cpsc

External ID

21729

Action Date

2021-03-18

Status

Ongoing

Category

product

Product Description

This recall involves bottles of the prescription drug Evrysdi, a prescription medicine used to treat spinal muscular atrophy (SMA) in adults and children 2 months of age and older. The recalled 100 mL amber bottles have "Evrysdi (risdiplam) for oral solution," the dosage and "NDC 20242-175-07" on the front of the bottle labels.

Context & Analysis

Genentech, a member of the Roche Group, of South San Francisco, Calif. has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

How often does Genentech, a member of the Roche Group, of South San Francisco, Calif. have FDA actions?

Genentech, a member of the Roche Group, of South San Francisco, Calif. has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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