Sunstar Americas, Inc.

Complete recall history across all FDA and CPSC categories — 6 total recalls

Sunstar Americas, Inc. appears in recall records across 2 categories. 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 (2)

FDA drug safety enforcement actions by Sunstar Americas, Inc.

Date Product Reason Class
Dec 28, 2020 Paroex (Chlorhexidine Gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only... cGMP Deviations; FDA inspection of manufacturing facility observed potential ... Class II
Oct 27, 2020 Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only... Microbial Contamination of Non-sterile Products: contamination with Burkholde... Class I

Device Recalls (4)

FDA medical device enforcement actions by Sunstar Americas, Inc.

Date Product Reason Class
Jan 14, 2022 BUTLER Clear Dip, 12 bottles/case Product lacks premarket clearance. Class II
May 21, 2021 SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse, 300mL, SKU numbers 1775P, 1775R ... Products may be contaminated with micro-organisms Burkholderia cepacia and/or... Class II
Mar 23, 2021 SUNSTAR Butler Clear Dip, 16 FL OZ, SKU #716PA Product may be contaminated with Burkholderia contaminans. Class II
Feb 18, 2021 SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray, 2 FL.OZ. UPC0 70... The product may be contaminated with Burkholderia cepacia 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.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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