How many inspections has Orlando Novelty LLC in Premier Row Orlando had?

Orlando Novelty LLC in Premier Row Orlando has 3 FDACS food safety inspection(s) on record from January 2022 to present.

What did the most recent FDACS inspection of Orlando Novelty LLC in Premier Row Orlando find?

Orlando Novelty LLC in Premier Row Orlando was most recently inspected by FDACS on June 17, 2025 (Product Re-inspection Required).

Has Orlando Novelty LLC in Premier Row Orlando had any stop-sale or stop-use orders?

Yes, Orlando Novelty LLC in Premier Row Orlando has 527 stop-sale or stop-use enforcement action(s) on record with Florida FDACS. Most affected products were voluntarily destroyed.

Orlando Novelty LLC in Premier Row Orlando

Name: Orlando Novelty LLC in Premier Row Orlando Inspection Records
Creator: Florida Department of Agriculture and Consumer Services
License: https://creativecommons.org/publicdomain/zero/1.0/

1624, Premier Row Orlando, FL 32809

Dry Storage · FDACS
FDACS Estab #: 393162

Overview

Orlando Novelty LLC in Premier Row Orlando, FL has 3 FDACS food safety inspections on record with 13 violations and 527 stop-sale or stop-use enforcement actions.

3FDACS Insp.

13Violations

527Stop-Sale Orders

Last inspected FDACS: June 17, 2025

Orlando Novelty LLC in Premier Row Orlando: FDACS Inspection History (3)

Inspections conducted by the Florida Department of Agriculture and Consumer Services (FDACS), which oversees grocery stores, convenience stores, bakeries, food manufacturers, mobile vendors, and vending machines.

2025 — 1 inspection

Jun 17, 2025 — Product Re-inspection Required· 13 violations· 527 stop-sale orders· Re-Inspection Required

Inspector: HANNAH BRUT, ENVIRONMENTAL SPECIALIST III

Comments: Stop Sale Order issued. Food establishment may visit https://foodpermit.fdacs.gov or contact the Business Center at (850) 245-5520 to request a written release of the Stop Sale Order. If the product contains a controlled substance, a court order obtained by a law enforcement agency may be required before the Department may release the product for destruction. Failure to obtain a written release from the Department prior to moving the stopped product or failure to comply with the terms of the Department's written release will result in Administrative Action.

Risk-Based Violations

70 A valid food license/permit and the most recent food safety or health inspection report from the approved source was not provided to the department upon request. 5K-4.034(4)(a), F.A.C.

A valid food license/permit and the most recent food safety or health inspection report from the approved source was not provided to the department upon request for multiple hemp extract products intended for ingestion. 5K-4.034(4)(a), F.A.C. See Stop Sale Order for products. o

70 A valid license/permit and the most recent inspection report from the permitting source was not provided to the department upon request. 5K-4.034(4)(b), F.A.C.

A valid license/permit and the most recent inspection report from the permitting source was not provided to the department upon request for hemp extract product intended for inhalation. 5K-4.034(4) (b), F.A.C. See Stop Sale Order for products. o

71 Hemp or Hemp Extract intended for Human Consumption sold or distributed in a container that is not compliant with ASTM International D3475-20, Standard Classification of Child Resistant Packages, because the container does not meet one or more of the descriptions of child-resistant packages set out in Table 1 therein. 5K-4.034(6)(j), F.A.C.

Multiple hemp extract products intended for Human Consumption sold or distributed in a container that is not compliant with ASTM International D3475-20, Standard Classification of Child Resistant Packages, because the container does not meet one or more of the descriptions of child-resistant packages set out in Table 1 therein. 5K-4.034(6)(j), F.A.C. See Stop Sale Order for products. o

75 Hemp extracted intended solely for inhalation is not clearly labeled with the statement "Not Intended For Ingestion - Do Not Eat". 5K-4.034(6)(e), F.A.C.

Multiple hemp extract products intended solely for inhalation are not clearly labeled with the statement "Not Intended For Ingestion - Do Not Eat." 5K-4.034(6)(e), F.A.C. See Stop Sale Order for products. o Print Date: 7/1/2025 Page 1 of 3 75 Citation Description: The label for retail products containing Hemp or Hemp Extract intended for Human Consumption does not include the serving size and servings per container expressed in Common Household Measures and the net contents expressed in both the appropriate International System of Units (SI) and United States customary units. 5K-4.034(6)(f), F.A.C. Observation: The label for multiple hemp extract products intended for Human Consumption does not include the serving size and servings per container expressed in Common Household Measures and the net contents expressed in both the appropriate International System of Units (SI) and United States customary units. 5K-4.034(6)(f), F.A.C. See Stop Sale Order for products. o

75 Hemp and hemp extract intended for human consumption does not declare the number of milligrams of each cannabinoid per serving and the serving size on the label. 5K-4.034(6)(c), F.A.C.

Multiple hemp extract products intended for human consumption do not declare the number of milligrams of each cannabinoid per serving and the serving size on the label. 5k-4.034(6)(c). See Stop Sale Order for products. o

75 The label of a product containing Hemp or Hemp Extract intended for Human Consumption in packaged form does not specify conspicuously the name and place of business of the processor, packer, or distributor. 5K-4.034(6)(i), F.A.C.

The labels of multiple products containing Hemp or Hemp Extract intended for Human Consumption in packaged form do not specify conspicuously the name and place of business of the processor, packer, or distributor. 5K-4.034(6)(i), F.A.C. See Stop Sale Order for products. o

75 Hemp or Hemp Extract intended for human consumption is distributed or sold in packaging that does not include: 1. A scannable barcode or quick response code linked to the certificate of analysis of the hemp extract by an independent testing laboratory; 2. The batch number; 3. The Internet address of a website where batch information may be obtained; 4. The expiration date; 5. The number of milligrams of each marketed cannabinoid per serving. s. 581.217(7)(a)2. a. - e., F.S. and 5K-4.034(6)(a), F.A.C.

Multiple hemp extract products intended for human consumption is distributed or sold in packaging that does not include: 1. A scannable barcode or quick response code linked to the certificate of analysis of the hemp extract by an independent testing laboratory; 2. The batch number; 3. The Internet address of a website where batch information may be obtained; 4. The expiration date; 5. The number of milligrams of each marketed cannabinoid per serving. s. 581.217(7)(a)2. a. - e., F.S. and 5K-4.034(6)(a), F.A.C. See Stop Sale Order for products. o

75 Hemp or Hemp extract intended for human consumption distributed or sold in the state not labeled pursuant to s. 500 F.S., s. 581.217(7) F.S., 5K-4.034(6)(a), F.A.C.

Hemp extract product intended for ingestion lacks nutritional labeling pursuant to s. 500 F.S., s. 581.217(7) F.S., 5K-4.034(6)(a), F.A.C. See Stop Sale Order for product. o

77 Hemp or Hemp Extract intended for Human Consumption distributed or sold in a container that is attractive to children as provided in 581.217, F.S. 5K-4.034(6)(b), F.A.C.

Multiple hemp extract products intended for Human Consumption distributed or sold in a container that is attractive to children as provided in 581.217, F.S. 5K-4.034(6)(b), F.A.C. Stop Sale Order for products. o

77 Hemp or hemp extract for human consumption is attractive to children, containing color additives. 581.217(3)(a) F.S., 5K-4.034(5), F.A.C.

Multiple hemp extract products for human consumption found to be attractive to children, containing color additives. 581.217(7)(3)(a) F.S., 5K-4.034(5), F.A.C. See Stop Sale Order for products. o INSPECTION: STATUTE-RULE Violation No.

91 The food establishment did not register as a Food Facility with the United States Food and Drug Administration (FDA) prior to beginning of manufacturing/processing, packing or holding food for consumption in the United States. 5K-4.002(D) F.A.C., 21 CFR 1, Subpart H.Repeat

You did not register as a Food Facility with the United States Food and Drug Administration. Registration information provided at time of inspection. Repeat COS o 92 Citation Description: Food is deemed misbranded as provided in 500.11, F.S. Observation: The following products are not labeled as required: 1) The allergen "contains" statement on the labels for Zombi "Cookies & Cream White Chocolate Bar" in the 15g size and the 50g size fail to declare the allergen of wheat. 2) The labels for lil' MFs tablets in "Blue Razz," "Sour Apple," and "Fruit Punch" contain a supplement facts panel but do not bear a statement that it is a "dietary supplement" or equivalent term. Further, the quantitative amounts by weight per serving of these dietary ingredients are not listed in the Supplement Facts panel. Additionally, the sub-ingredients of the ingredient "Psilocybin Free Magic Mushroom Extract" are not declared. 3) The labels for The Good Fellows chocolate bars in "Strawberry Crunch," "Dark Chocolate Monster Blend," "Cookies and Cream," and "Euphoria" contain a supplement facts panel but do not bear a statement that it is a "dietary supplement" or equivalent term. 4) The labels for Allitom CBN CBD Gel Caps contain a supplement facts panel, but it is labeled as "Product Facts" and not "Supplement Facts." Further, these labels do not bear a statement that it is a "dietary supplement" or equivalent term. o

97 Food bears or contains a poisonous or deleterious substance which may render it injurious to health. 500.10(1)(a), F.S.

Multiple Silly Farms branded chocolate and white chocolate bars found to contain amanita extract (muscimol). See Stop Sale Order for products. o

98 The product intended for human consumption contains a total delta-9 tetrahydrocannabinol concentration of more than 0.3% on a wet-weight basis and therefore does not meet the definition of hemp or hemp extract. The product is considered adulterated pursuant to s. 500.10(1)(a), and s. 581.217(3)(e), F.S. and contains a controlled substance pursuant to s. 893.03(1)(c)190.a., F.S.

Hemp extract products observed to be over the 0.3% total delta 9 THC concentration according to product package labeling or Certificate of Analysis. See 581.217(3)(e), F.S., and Rule 5k-4.034(2)(m). o A Supplemental Report was also issued during the visit which includes important information for management.