Reported Jan 3, 2024 · Terminated

Ipratropium Bromide and Albuterol Sulfate Inhalation Solution (0.5 mg/3 mg per 3 mL), 60 x 3 mL Sterile Unit-Dose Vials…

Cardinal Healthcare

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: CARDINAL HEALTHCARE · 7200 Cardinal Pl W · Dublin, OH · 43017-1094

Is this the product you have?

  • Ipratropium Bromide and Albuterol Sulfate Inhalation Solution (0.5 mg/3 mg per 3 mL), 60 x 3 mL Sterile Unit-Dose Vials (2 pouches of 30 - 3 mL vials each)
  • Manufactured ByThe Ritedose Corporation, Columbia, SC 29203
  • Distributed By
    • Cipla USA Inc
    • 10 Independence Boulevard
    • Suite 300
    • Warren
    • NJ 07059
  • NDC69097-840-64
Lot codes and dates
  • Batch 21C56
Amount recalled
2 cartons

This recall covers 42 products

The agency filed one notice per product. You are reading one of them; the other 41 are below.

29 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Cardinal Healthcare recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Sep 29, 2024 · Data as of Sep 19, 7:23 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.