Current FDA corpus

Search recall evidence

Search official identifiers, recalled products, recalling firms, recall reasons, distribution language, and available device root-cause evidence.

Product, firm, identifier, or evidence phrase

Result scope

Ordinary terms are combined with AND. Put a literal phrase in quotation marks. Raw operators, wildcards, field syntax, and repeated controls are rejected.

All · Relevance

Results for “nationwide distribution”

35,881 true results · 25 per page

Events: 8,763
Products: 24,938
Firms: 2,180

Products

24,938 true total · 25 on this page

Recalled product

Adrenal Test

Z-0772-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Syphilis Test

Z-0751-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Parasite Test

Z-0748-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Chlamydia Test

Z-0730-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Pregnancy Test

Z-0749-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Estrogen & Progesterone Test

Z-0805-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Allergy test Small

Z-0803-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Leaky Gut Test

Z-0787-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Gonorrhea test

Z-0738-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Liver Test

Z-0801-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Food Intolerance Test Small

Z-0808-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Vitamin D-Test

Z-0756-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Food Intolerance Test Medium

Z-0807-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Blood Type Test

Z-0728-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Biological Age & Longevity Test

Z-0774-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Food Sensitivity Test Medium

Z-0761-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Iron Deficiency Test (ferritin)

Z-0811-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Men s Hormone Test

Z-0788-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

GI Microbiome Profile XL

Z-0764-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Gut Microbiome Test Medium

Z-0779-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Gut Microbiome Test Small

Z-0781-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Trichomonas Vaginalis test

Z-0753-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Gut Microbiome Test XL

Z-0782-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

D-Dimer Test

Z-0731-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

GI Microbiome Profile Small

Z-0763-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II