Skip to content

Trojan Premium Latex Condoms Magnum Large Size Condoms recallZ-1181-2026 · Gold Star Distribution Inc · initiated Dec 26, 2025

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Gold Star Distribution Inc or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

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

FDA root cause category: Storage

What the company is doing

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.

Recall details

Recall number
Z-1181-2026
Status
Open, Classified
Initiated by the company
Dec 26, 2025
Posted by the FDA
Jan 27, 2026
Recalling firm
Gold Star Distribution Inc
Quantity
unknown
Product code
HIS
FDA submissions
K874383
Distribution
US Nationwide distribution in the states of Minnesota.

Product description

Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, TROJAN CONDOMS MAGNUM 48 CT DISP, *BOX TROJAN CONDOMS MAGNUM 50CT .

Code information (models, lots, serial numbers)

TROJAN MAGNUM CONDOMS 6/DSP BLACK, UPC 022600642039; TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, UPC 022600930501; TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, UPC 022600931508; TROJAN ULTRA THIN CONDOMS 6/DSP GREY, UPC 022600926207; TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, UPC 022600940500; TROJAN NONLUBRICATED CONDOMS 6/DSP RED, UPC 22600920502; TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, UPC 022600973201; TROJAN CONDOMS MAGNUM 48 CT DISP, UPC 815556020125; *BOX TROJAN CONDOMS MAGNUM 50Ct, UPC none All codes purchased from this firm

Devices named in this recall

6 devices in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Other products in the same recall event

The FDA groups related products into one recall event (event 98234).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page