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

Food Intolerance Test Large

Z-0806-2026

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 Small

Z-0762-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Thyroid TSH Test

Z-0752-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Allergy & Food Intolerance Test

Z-0802-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Women s Hormone Test

Z-0798-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Sorbitol Intolerance Test

Z-0797-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Environmental Pollutants Profile Test

Z-0758-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Vaginal PH Test

Z-0755-2026

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 IgE

Z-0769-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Diabetes HbA1c Test

Z-0732-2026

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 Large

Z-0760-2026

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

Z-0742-2026

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 Large

Z-0778-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

HPV Antigen Test

Z-0741-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Female Fertility Test

Z-0737-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Menopause (FSH) 2 Tests

Z-0744-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Urinary Tract Infection Test

Z-0754-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Organic Acids Profile Test Large

Z-0767-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Food Allergy Panel Test (IgE)

Z-0759-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Diabetes Test (ketones & glucose)

Z-0799-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Fecal Occult Blood Test

Z-0736-2026

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 Mega

Z-0780-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Continuous Glucose Monitor (CGM)

Z-0770-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Vitamin D2 and D3 Test

Z-0768-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Ovulation Test (5 tests)

Z-0747-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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