Geritrex recalls

Geritrex has 15 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 31 Jul 2019. The most frequent reason is sterility.

Total recalls15since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 31 Jul 2019

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 14 93%Class III 1 7%

By year

All geritrex recalls, newest first

15 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIPreferred Plus Pharmacy Iron Elixir Ferrous Sulfate, 220 mg recalledGeritrexSterilityNationwide
DrugCLASS IIRitussin DM Children & Adults recalled by GeritrexGeritrexSterilityNationwide
DrugCLASS IIRitussin DM Double Strength recalled by GeritrexGeritrexSterilityNationwide
DrugCLASS IIGericare Iron Supplement Elixir Ferrous Sulfate, 220 mg recalledGeritrexSterilityNationwide
DrugCLASS IIDiphenhydramine Oral Liquid Alcohol Free, 12.5 mg recalled by GeritrexGeritrexSterilityNationwide
DrugCLASS IIGericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg recalledGeritrexSterilityNationwide
DrugCLASS IIGericare Geri-Tussin DM, Geri-care Phamaceuticals Corp recalledGeritrexSterilityNationwide
DrugCLASS IIPreferred Plus Dioctyl Liquid Stool Softener recalled by GeritrexGeritrexSterilityNationwide
DrugCLASS IISenna (sennosides 8.8 mg) Syrup recalled by GeritrexGeritrexPotency & AssayNationwide
DrugCLASS IISenna (sennosides 8.8 mg) Syrup recalled by GeritrexGeritrexPotency & AssayNationwide
DrugCLASS IICarbo-O-Philic 40 Gel 40% (Urea) recalled by GeritrexGeritrexLabeling ErrorsNationwide
DrugCLASS IIPolyethylene Glycol 3350-GRX Powder 100% jars a) recalled by GeritrexGeritrexLabeling ErrorsNationwide
DrugCLASS IICarbo-O-Philic 40 Cream 40% (Urea) tubes, a) recalled by GeritrexGeritrexLabeling ErrorsNationwide
DrugCLASS IIGRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories recalledGeritrexLabeling ErrorsNationwide
DrugCLASS IIICarb-O-Philic 40 Cream, 40%, a) tube recalled by GeritrexGeritrexManufacturing (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.