FDA recall D-250-2013

Product

Children's Acetaminophen Oral Suspension, 650 mg/20.3 mL unit dose cup (NDC 68094-650-59), packaged in 30-count cups per shipper case (NDC 68094-650-62), Pkg. By: Precision Dose, Inc., S. Beloit, IL 61080.

Reason for recall

Labeling: Not Elsewhere Classified: This unit dose product is being recalled because the product's name includes the word "Children's" which is misleading since the 650 mg dose of acetaminophen contained within it, is an adult dose.

Distribution

Nationwide and Puerto Rico

Key facts

Status

Terminated

Initiation date

2013-03-21

Report date

2013-04-24

Termination date

2015-05-07

Voluntary/Mandated

Voluntary: Firm initiated

Location

South Beloit, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-250-2013