Z-1180-2026 Class II Ongoing

Recalled by GOLD STAR DISTRIBUTION INC — Minneapolis, MN

FDA device recall Z-1180-2026 was initiated by GOLD STAR DISTRIBUTION INC on Dec 26, 2025 and is designated Class II. Reason for recall: Potential exposure of rodents and rodent activity in the distribution center. The recall status is ongoing.

Recall Details

Product Type
Devices
Report Date
Feb 4, 2026
Initiation Date
Dec 26, 2025
Voluntary/Mandated
Voluntary: Firm initiated

Product Description

Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT

Reason for Recall

Potential exposure of rodents and rodent activity in the distribution center.

Distribution Pattern

US Nationwide distribution in the states of Minnesota.

Code Information

FIRST AID KIT 24/42PC, UPC 808829102536; LUCKY FIRST AID BANDAGES 24CT, UPC 808829041002. All codes purchased from this firm

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1180-2026
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for Z-1180-2026. Report a data issue: hello@regdatalab.com.