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Recall Observatory FDA recall evidence

Current FDA corpus

Search recall evidence

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

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Results for “nationwide distribution”

35,881 true results · 25 per page

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

Events

8,763 true total · 4 on this page

Recall event

Event 89658

89658
Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date
February 18, 2022
Product type
Device
Classification
Class II
Matching products
1

Recall event

Event 85729

85729
Matched recall reason

Recall reason · … Philips is therefore removing this device from distribution.

Represented date
May 19, 2020
Product type
Device
Classification
Class II
Matching products
1

Recall event

Event 97896

97896
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date
November 03, 2025
Product type
Device
Classification
Class II
Matching products
92

Products

24,938 true total · 18 on this page

F-0783-2014
Matched product description

Product description · … quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83314);

Represented date
October 30, 2013
Product type
Food
Classification
Class II
Z-0822-2022
Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date
February 18, 2022
Product type
Device
Classification
Class II
D-0285-2026
Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

Represented date
December 26, 2025
Product type
Drug
Classification
Class II
F-0799-2014
Matched product description

Product description · … quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92473);

Represented date
October 30, 2013
Product type
Food
Classification
Class II
F-0787-2014
Matched product description

Product description · … within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92275); (2) ActiFIT, Actizyme, Digest …

Represented date
October 30, 2013
Product type
Food
Classification
Class II
D-0286-2026
Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

Represented date
December 26, 2025
Product type
Drug
Classification
Class II

Recalled product

Iodine Test

Z-0810-2026
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

SIBO Test

Z-0796-2026
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Candida Test

Z-0775-2026
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

IBS Test

Z-0784-2026
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Akkermansia Test

Z-0773-2026
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Recalled product

Melatonin Test

Z-0812-2026
Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

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

Firms

2,180 true total · 3 on this page

dollar tree distribution inc
Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date
October 05, 2023
Product type
Device
Classification
Class II
Matching products
4
philips north america llc
Matched recall reason

Recall reason · … Philips is therefore removing this device from distribution.

Represented date
June 05, 2026
Product type
Device
Classification
Class II
Matching products
332

FDA name variants: Philips North America Llc · Philips North America, LLC · Philips North America LLC

d b p distribution
Matched recalling firm

Recalling firm · D.B.P. Distribution

Represented date
April 23, 2019
Product type
Drug
Classification
Class I
Matching products
1