There is a dog supplement tub in your cupboard. You see a Fi recall headline and suddenly the ordinary label looks like a puzzle. The brand name alone will not answer the question. You need the product name and lot number.
First, check the exact product and lot
The FDA notice lists two products. Both are 180 g tubs. The lot number is the decisive detail, not a photo that merely looks similar to your container.
| Product in FDA notice | Lot number | UPC |
|---|---|---|
| Fi Calming supplement for Dogs, 180 g | 26118 | 8 50064 80011 1 |
| Fi 8-in-1 Formula supplement for Dogs, 180 g | 26159 | 8 50055 11168 4 |

Find the lot printed on the package and compare every digit with the FDA table. The UPC is a second way to identify the product, but it does not replace the lot check. If the print is smudged or missing, do not guess from the color of the tub. Keep the product aside and ask Fi directly using the contact details in the official notice.

The announcement says these lots were distributed directly to consumers and through Amazon and Chewy. If you ordered online, the order history can help you identify when and where you bought the tub, but the code on the actual container remains the check that matters.
What to do if your container matches
The company’s instructions are direct: discontinue use, make sure the container is tightly sealed, and dispose of it in the trash. Do not give the rest to another dog, and do not leave the tub where a pet can investigate it.

Photograph the product name, lot code and UPC before disposal if you may need them when contacting the company or veterinarian. That is a practical record-keeping step, not an FDA requirement. Fi lists 1-888-434-3647 (10 a.m. to 8 p.m. Eastern, seven days a week) and support@tryfi.com for consumer questions in its announcement. Check the FDA page for any later change before calling.

Handle the tub carefully, wash your hands afterward, and clean any surfaces or bowls that may have contacted the supplement. The notice warns that Salmonella can affect dogs and people who handle contaminated products or animal waste.
What if your dog already ate it?
A matching lot is a reason to stop feeding the supplement. It does not mean your dog has a confirmed infection. The FDA notice says dogs with Salmonella infection may be lethargic or have diarrhea, sometimes bloody diarrhea, fever or vomiting. Some may show reduced appetite or abdominal pain. A dog can also carry the bacteria without looking sick.

If your dog ate a recalled lot and has these signs, contact your veterinarian. Tell them the product name and lot number, when it was eaten, and what has changed. If your dog seems seriously ill or deteriorates quickly, seek prompt veterinary care rather than waiting for a reply from the supplement company. Do not try to diagnose Salmonella from symptoms alone; many illnesses can look similar.

If your dog appears well, the recall still applies to the product. Stop using a matching lot and ask your veterinarian whether anything else is appropriate for your individual dog. A replacement supplement is not automatically needed. If a veterinarian recommended Fi for a particular issue, check with them before changing the broader care plan.
The human side of the recall
The FDA-posted announcement also warns about human exposure through handling the supplement, contact surfaces or animal waste. Wash hands after touching those items, and keep children away from the recalled product. People with symptoms such as diarrhea, fever or abdominal cramps after potential exposure should contact a healthcare professional.

Do not confuse this with a Fi smart collar recall. The notice is about the two named supplement lots, not all Fi products and not every supplement made by the brand. Broad warnings spread faster than careful ones; the product and lot are what make this notice useful.

Quick answers
Is every Fi dog supplement recalled? The FDA announcement identifies the two specific product-and-lot combinations in the table above. It does not say all Fi products are recalled.
My lot is different. Should I throw it away? A different lot is not identified in this notice. Recheck the code and current FDA page. Contact Fi if the code is unreadable or you have questions about your container.
Does “possible contamination” mean a dog has been infected? No. It is the reason for the recall, not a diagnosis of any particular dog. Contact your veterinarian if a dog that ate a recalled lot develops concerning signs.
Where should I check for updates? Use the FDA recall page. The company announcement was dated September 3, 2026 and published by FDA on September 8; a September 18 note corrected the company name to Fi Barking Labs Corp. This page was reviewed on September 29, 2026.

Bottom line: Check the tub, not the headline. The two lot numbers are 26118 and 26159. A match means stop using the supplement and follow Fi’s disposal instructions. Symptoms after exposure warrant a veterinarian’s advice.
Source: FDA-posted Fi company recall announcement, reviewed September 29, 2026. This article summarizes the announcement; it does not replace the current notice or individualized veterinary or human medical advice. Images are AI-generated editorial illustrations, not photos of the recalled product. No affiliate product is recommended here.

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