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Power Selles Imports dba Culinary Collective

Complete recall history across all FDA and CPSC categories — 9 total recalls

Power Selles Imports dba Culinary Collective 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.

Food Recalls (9)

FDA food safety enforcement actions by Power Selles Imports dba Culinary Collective

Date Product Reason Class
Mar 13, 2023 Matiz Piparra Peppers are packaged in a clear glass jar, net wt. 4lb. (1.8kg)... A shard of glass being found in one of the jars. Class II
Feb 6, 2023 Arroyabe Bonito Flakes White Meat Tuna Flakes in Oil From the Basque region o... Dried fish bones were found in product. Class II
May 5, 2022 Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt.... Potential contamination with peanut while label does not declare peanut. Class I
Apr 29, 2022 Valencian Almonds with TRUFFLE FS distributed in bulk case, each case contain... Foreign materials. Class II
Dec 13, 2021 ZOCALO AJI LIMO DRIED CHILI PODS- ORGANIC, Dried Aji Peppers for consumer con... Due to presence of mold on product Class II
Mar 17, 2021 Blanxart Milk Chocolate with Hazelnuts Cacao 33% Min. Net wt.7 oz. Product is... Metal fragment. The small thin metal piece is around 0.5 inch long without s... Class II
Aug 27, 2020 Blanxart 82% Congo Organic Chocolate Bar. Paper packaging with internal foil ... A foreign object found by a consumer in a chocolate bar. Class II
Jun 23, 2020 Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packagin... A foreign object found by a consumer in dark chocolate bar. Class II
Jul 24, 2018 Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar, packaged in shrink wrap pla... Matiz Apricot Bar Demi-luna 8.8 ounces bar is recalled because customer found... 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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