Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Summary
The FDA issued a Class II for Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24 by GOLD STAR DISTRIBUTION INC. Reason: Potential exposure of rodents and rodent activity in the distribution center..
Details
Source
Device Recall
External ID
Z-1180-2026
Action Date
2026-02-04
Status
Ongoing
Category
device
Product Description
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Lot/Code Info: FIRST AID KIT 24/42PC, UPC 808829102536; LUCKY FIRST AID BANDAGES 24CT, UPC 808829041002. All codes purchased from this firm
Quantity Affected: unknown
Reason for Recall
Potential exposure of rodents and rodent activity in the distribution center.
Distribution
US Nationwide distribution in the states of Minnesota.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-12-26
Company
Minneapolis, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 175 device recalls issued in the same week, part of 403 device-related FDA actions this month.
GOLD STAR DISTRIBUTION INC has 33 FDA actions in our database, including 33 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GOLD STAR DISTRIBUTION INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GOLD STAR DISTRIBUTION INC have FDA actions?
GOLD STAR DISTRIBUTION INC has 33 FDA actions in our database, including 33 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1180-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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