Time-Cap Laboratories recalls

Time-Cap Laboratories has 12 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 2 May 2018. The most frequent reason is manufacturing (cgmp) deviations.

Total recalls12since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 2 May 2018

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 12 100%Class III 0 0%

Why time-cap laboratories is recalled

Product types

By year

All time-cap laboratories recalls, newest first

12 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIbuprofen Caplets USP 200 mg, a) 50 caplets recalledIbuprofenTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets, USP, 200 mg, a) recalled by Time-Cap LaboratoriesIbuprofenTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets USP 800 mg, a) recalled by Time-Cap LaboratoriesTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets USP 400 mg bottles recalled by Time-Cap LaboratoriesTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Caplets USP 200 mg, a) 50 caplets recalledIbuprofenTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets, USP, 200 mg, a) recalled by Time-Cap LaboratoriesIbuprofenTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets USP 600 mg, a) recalled by Time-Cap LaboratoriesIbuprofenTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets USP 600 mg, a) recalled by Time-Cap LaboratoriesTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets USP 600 mg, a) recalled by Time-Cap LaboratoriesTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIIbuprofen Tablets USP 400 mg, a) recalled by Time-Cap LaboratoriesIbuprofenTime-Cap LaboratoriesManufacturing (CGMP) DeviationsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.