FDA Drug Recalls

Recalls / Class II

Class IID-0691-2018

Product

Ibuprofen Tablets USP 600 mg, a) 100 tablet (NDC 42582-112-01), b) 500 tablet bottles (NDC 42582-112-18), Rx, Distributed by Drug Mart, Food Fair, Medina, Ohio 44256

Affected lot / code info
a) C135C, exp 3/18 b) C134C, exp 3/18

Why it was recalled

CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.

Recalling firm

Firm
Time-Cap Laboratories, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
7 Michael Ave, N/A, Farmingdale, New York 11735-3921

Distribution

Quantity
N/A
Distribution pattern
Nationwide.

Timeline

Recall initiated
2018-01-11
FDA classified
2018-04-22
Posted by FDA
2018-05-02
Terminated
2021-01-20
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0691-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.