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FDA Medical Device Recalls (openFDA)

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

Recall number
Z-1180-2026
Recalling firm
GOLD STAR DISTRIBUTION INC
Product
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Status
Open, Classified
Initiated
2025-12-26
Posted
2026-01-27
Terminated
not on file
Reason
Potential exposure of rodents and rodent activity in the distribution center.
Root cause
Storage
Action
Gold Start Distribution, Inc. issued a press release on 12/26/2025 to notify the public of their recall of FDA regulated products due to the presence of rodent and avian contamination. The press release explained the risk to health, provided a list of retail outlets to which the products were distributed, and directed those in possession of the affected product to destroy them and verify such destruction by receipt provided to Gold Start at 1000 N. Humboldt Ave, Minneapolis, MN 55411. Refunds will be provided upon request. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products. If you have any questions, contact Gold Star at 612-617-9800, 7 days a week, 8:00 am to 5:00 pm, Central Standard Time. The firm followed with a letter to its consignees on 12/30/2025 via email with the same message.
Quantity
unknown
Distribution
US Nationwide distribution in the states of Minnesota.
Lot, serial or model codes
FIRST AID KIT 24/42PC, UPC 808829102536; LUCKY FIRST AID BANDAGES 24CT, UPC 808829041002. All codes purchased from this firm
510(k) numbers
not on file
PMA numbers
not on file
Product code
KGX
Firm FEI
3004388746
Firm city
Minneapolis
Firm state
MN
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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