Back to search
FDAFDA · Food and drugs·Recall number D-1021-2022

Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution 3mL vial, packaged in a) 30-count (NDC 0487-0201-03), b) 60-count (NDC 0487-0201-60), Rx only, MFG: Nephron Pharma

Published June 15, 2022 · Recall initiated: April 13, 2022

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

cGMP deviations: Temperature abuse

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE
Manufacturer
Mckesson Medical-Surgical Inc. Corporate Office
Distributor
USA nationwide.
UPC
0304870201018
Lot
McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Risk classification
Class III
Area (FDA)
drug
Country
United States

Sell products like this?

Recalert watches your whole catalog for recalls like this one, automatically.

Start free — no card