RIJ Pharmaceutical recalls

RIJ Pharmaceutical has 12 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 20 Jun 2018. The most frequent reason is potency & assay.

Total recalls12since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 20 Jun 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 rij pharmaceutical is recalled

By year

All rij pharmaceutical recalls, newest first

12 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIGericare Diocto Liquid (Docusate Sodium 50mg), 50 mg recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IISDA Senna Syrup (Sennosides 8.8mg) recalled by RIJ PharmaceuticalSenna SyrupRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIRitussin DM Dextromethorphan Hydrobormide recalled by RIJ PharmaceuticalRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIGeriCare Senna Syrup (Sennosides 8.8 mg), Dist recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIPreferred Plus Pharmacy Antacid (Aluminum Hydroxide 200mg recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIRPC APAP Elixir (Acetaminophen 160mg) recalled by RIJ PharmaceuticalRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIGericare Iron Supplement Elixir Ferrous Sulfate 220 mg recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIRPC Senna Syrup (Sennosides 8.8mg) recalled by RIJ PharmaceuticalRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIGericare Liquid Pain Relief Acetaminophen Cherry Flavor 160mg recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIRPC Children's Non-Aspirin (Acetaminophen 160 mg) Elixir recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIPreferred Plus Pharmacy Antacid Extra Strength recalledRIJ PharmaceuticalPotency & AssayNationwide
DrugCLASS IIGeritrex Senna Syrup (sennosides 8.8mg) recalled by RIJ PharmaceuticalRIJ PharmaceuticalPotency & AssayNationwide

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.