GOLD STAR DISTRIBUTION INC

FDA recalling firm · 3 enforcement events · 33 product records · 2025–2025 · MN

GOLD STAR DISTRIBUTION INC has 3 FDA enforcement events on this register (33 product records) between 2025 and 2025: 1 device, 1 drug and 1 food; the busiest year was 2025 with 3.

0% of its events are Class I; the most common class is Class II (3). 3 events are listed as ongoing; the recalling firm's address is in MN.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
26 Dec 2025	Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT	Device	Class II	5	Ongoing
26 Dec 2025	Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559	Drug	Class II	27	Ongoing
26 Dec 2025	All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces,…	Food	Class II	1	Ongoing

By type and class

Device1

Drug1

Food1

Class II3

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for GOLD STAR DISTRIBUTION INC by year initiated.

Questions and answers

How many FDA recalls has GOLD STAR DISTRIBUTION INC had?

3 enforcement events (33 product records) on this register, 2025–2025: 1 device, 1 drug, 1 food.

Are any GOLD STAR DISTRIBUTION INC recalls ongoing?

3 events are listed as ongoing in the current openFDA export.

What class are GOLD STAR DISTRIBUTION INC recalls?

3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.