Medique Products

FDA Regulatory Profile

Medique Products appears in FDA public data with 3 recalls, 0 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0390-2022, Class II) was initiated on December 6, 2021.

Summary

Total Recalls
3
510(k) Clearances
0
Inspections
3
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0390-2022Class IIMedique Pain-Off (Acetaminophen 250 mg, Aspirin (NSAID*) 250 mg, Caffeine 65 mg) Tablets, packaged iDecember 6, 2021
D-0391-2022Class IIExtra Strength Headache (acetaminophen 250 mg, aspirin 250 mg, caffeine 65 mg) tablets, packaged in December 6, 2021
D-0389-2022Class IIPhysicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg,December 6, 2021