Class II · ModerateRecall completed
Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml)
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberBatch: 1GK0905, Exp 01/31/2023
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Perrigo Company PLC |
| NDC | 37808-759-26 |
Show the full FDA record
| Full product label | Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, MADE WITH PRIDE & CARE FOR H-E-B SAN ANTONIO, TX 78204. NDC: 37808-759-26 |
| Recalling firm | Perrigo Company PLC |
| Distribution | Nationwide in the USA |
| Quantity | 3,840 bottles |
| Recall initiated | 2021-10-26 |
| Report date | 2022-03-02 |
| Recall completed | 2023-09-29 |
| Recall number | D-0593-2022 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Allegan MI United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.