RIJ Pharmaceutical LLC
Complete recall history across all FDA and CPSC categories — 12 total recalls
RIJ Pharmaceutical LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Drug Recalls (12)
FDA drug safety enforcement actions by RIJ Pharmaceutical LLC
| Date | Product | Reason | Class |
|---|---|---|---|
| May 7, 2018 | Gericare Diocto Liquid (Docusate Sodium 50mg), 50 mg/5 mL, packaged in 16 FL ... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | SDA Senna Syrup (Sennosides 8.8mg), packaged in 8 FL. OZ. (236 mL) bottles, D... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | Ritussin DM Dextromethorphan Hydrobormide (Dextromethorphan HBr, USP 10 mg, G... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | GeriCare Senna Syrup (Sennosides 8.8 mg), 8 fl oz (237 mL) bottles, Dist, by ... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | Preferred Plus Pharmacy Antacid (Aluminum Hydroxide 200mg, Magnesium Hydroxid... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | RPC APAP Elixir (Acetaminophen 160mg), Packaged in 16 FL. OZ. (473 mL) bottle... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | Gericare Iron Supplement Elixir Ferrous Sulfate 220 mg, packaged in 16 fl oz.... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | RPC Senna Syrup (Sennosides 8.8mg), packaged in 8 fl oz (237 mL) bottles, RIJ... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | Gericare Liquid Pain Relief Acetaminophen Cherry Flavor 160mg/5mL, packaged i... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | RPC Children's Non-Aspirin (Acetaminophen 160 mg) Elixir, packaged in 4 FL. O... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | Preferred Plus Pharmacy Antacid Extra Strength (Aluminum Hydroxide 400mg, Mag... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
| May 7, 2018 | Geritrex Senna Syrup (sennosides 8.8mg), packaged in 8 FL OZ. (236 mL) bottle... | CGMP Deviations: Products are being recalled due to an out of specification t... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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