CLASS II ONGOING Device recall · Reported 4 Feb 2026 · FDA Enforcement Report
Bandages and first aid kits: First Aid Kit 24/42PC recalled
Gold Star Distribution is recalling Bandages and first aid kits: First Aid Kit 24/42PC, Lucky First Aid Bandages, distributed nationwide in the US. The recall was initiated on 26 Dec 2025 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1180-2026
- FDA event ID
- 98234
- Recalling firm
- Gold Star Distribution, Minneapolis, MN
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 26 Dec 2025
- FDA classified
- 27 Jan 2026
- Reported
- 4 Feb 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Foreign Material
- Device type
- Other Medical Devices
Timeline
| 26 Dec 2025 | Recall initiated by company | |
| 27 Jan 2026 | Classified by FDA | +32 days |
| 4 Feb 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential exposure of rodents and rodent activity in the distribution center.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Where it was distributed
US Nationwide distribution in the states of Minnesota.
Questions about this recall
Why was it recalled?
Potential exposure of rodents and rodent activity in the distribution center.
Which lots are affected?
FIRST AID KIT 24/42PC, UPC 808829102536; LUCKY FIRST AID BANDAGES 24CT, UPC 808829041002. All codes purchased from this firm
Where was it sold?
US Nationwide distribution in the states of Minnesota.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
4 other products · FDA event 98234This product is part of a recall event; the main page for the event is Feminine hygiene products, labeled as recalled by Gold Star Distribution.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Feminine hygiene products, labeled as recalled by Gold Star Distribution | Gold Star Distribution | Foreign Material | Nationwide | |
| CLASS II | Toothbrushes, labeled as: Oral B Tooth Brush Shiny Clean Soft recalled | Gold Star Distribution | Foreign Material | Nationwide | |
| CLASS II | Condoms, labeled as: Trojan Magnum Condoms 6/Dsp Black recalled | Gold Star Distribution | Foreign Material | Nationwide | |
| CLASS II | Pregnancy Test recalled by Gold Star Distribution | Gold Star Distribution | Foreign Material | Nationwide |
More recalls from Gold Star Distribution
All 33| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Pregnancy Test recalled by Gold Star Distribution | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Condoms, labeled as: Trojan Magnum Condoms 6/Dsp Black recalled | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Toothbrushes, labeled as: Oral B Tooth Brush Shiny Clean Soft recalled | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Feminine hygiene products, labeled as recalled by Gold Star Distribution | Gold Star Distribution | Foreign Material | Nationwide |
| Food | CLASS II | All human food products distributed from the firm recalled | Gold Star Distribution | Foreign Material | IN, MN, ND |
Other Other Medical Devices recalls
All 13,884| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | NOxBOXi Nitric Oxide Delivery System recalled | Noxbox | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos R pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065 recalled | Percussionaire | Other | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-1C recalled by Percussionaire | Percussionaire | Other | Nationwide |