Associates of Cape Cod recalls Fungitell Kit (Catalog FT001) due to possible missing components. This affects kits sold with lot number FK180:18005. Consumers should check their kit's lot number and contact the company for remedy.
The kits may contain the incorrect number of components or the kits may be missing components.
Associates of Cape Cod is recalling Fungitell Kit (Catalog FT001) because some kits may be missing required components. This could affect the kit's ability to properly detect fungal infections in patients.
The kits may have incorrect component counts or missing parts. This could lead to inaccurate fungal infection testing results if the kit is used without all required components.
Patients using the Fungitell Kit for fungal infection testing may be affected. Those with the specific lot number FK18005 are most at risk.
Check the lot number on the kit, which is FK18005 for this recall. The product is sold under the catalog number FT001.
Look for the lot number FK18005 on the Fungitell Kit packaging.
The kits may contain the incorrect number of components or be missing required parts.
Check the lot number on the kit. If it's FK18005, contact Associates of Cape Cod for remedy instructions.
This recall is low risk as it only affects the kit's ability to test properly, not causing injury.
We’ve drafted a message you can send Associates of Cape Cod to request your refund or repair — edit it as you like.
Subject: Recall Z-1329-2019 — Associates of Cape Cod Associates of Cape Cod Hello, I own a Associates of Cape Cod that is covered by recall Z-1329-2019 from Associates of Cape Cod. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
