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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 · 7 on this page

Recall event

Event 65089

65089
Matched recall reason

Recall reason · In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.

Represented date
April 12, 2013
Product type
Device
Classification
Class II
Matching products
2

Recall event

Event 64496

64496
Matched recall reason

Recall reason · Blue Planet products that contain the two recalled Dakota Specialty Milling ingredients; distribution of recalled bulk, wholesale, and …

Represented date
February 19, 2013
Product type
Food
Classification
Class II
Matching products
7

Recall event

Event 73070

73070
Matched recalling firm

Recalling firm · Family Dollar Stores - NC Distribution Center

Represented date
September 08, 2015
Product type
Food
Classification
Class II
Matching products
2

Recall event

Event 86427

86427
Matched product description

Product description · … Oz. (472 mL) bottle, Made in Guatemala, Distributed by Central Med Distribution, 6100 Hollywood Blvd, Hollywood FL 33024 …

Represented date
September 11, 2020
Product type
Drug
Classification
Class II
Matching products
1

Recall event

Event 86432

86432
Matched product description

Product description · … PermaFlo contains H1¿m average particle size with narrow upper limit particle distribution.

Represented date
August 31, 2020
Product type
Device
Classification
Class II
Matching products
1

Recall event

Event 38329

38329
Matched recall reason

Recall reason · Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.

Represented date
June 14, 2007
Product type
Drug
Classification
Class II
Matching products
2

Recall event

Event 90050

90050
Matched recall reason

Recall reason · Product not approved for release for US distribution

Represented date
March 22, 2022
Product type
Device
Classification
Class II
Matching products
2

Products

24,938 true total · 12 on this page

Recalled product

Dietary Supplements packaged in the following configurations: (1)Transformation Professional Protocol Digest Enzyme Supplement, Packaged in 45-(SKU 54646), 60-(SKU 52413), 90-(SKU 52520), 120-(SKU 53098) capsule bottles. The firm name on the label is Transformation Enzyme Corp. Houston, TX; (2) 3989V TEC-TPP DIGEST UNL 60' unlabeled 60-(SKU 53571) capsule bottles; (3) Transformation Digest. Packaged in 60-(SKU 54599) capsule bottles. Russian label; (4) Anti-aging Nutrition Health Graph Professional Strength Digest Enzyme Supplement. Packaged in 120-(SKU 54752) bottles. The firm name on the label is Health Graph, Glenview, IL; (5) The Lohad Center for Anti-Aging Digest Enzyme Supplement. Packaged in 90-(SKU 54914) capsules bottles. The firm name on the label is The Lohad Center, Jacksonville, FL. (6) Bulk 3989V TPP-TEC Digest Conv Pa capsules (SKU 92494) packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution)

F-0739-2014
Matched product description

Product description · … in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution)

Represented date
October 30, 2013
Product type
Food
Classification
Class II
D-0037-2021
Matched product description

Product description · … Oz. (472 mL) bottle, Made in Guatemala, Distributed by Central Med Distribution, 6100 Hollywood Blvd, Hollywood FL 33024 …

Represented date
September 11, 2020
Product type
Drug
Classification
Class II
Z-0053-2021
Matched product description

Product description · … PermaFlo contains H1¿m average particle size with narrow upper limit particle distribution.

Represented date
August 31, 2020
Product type
Device
Classification
Class II

Firms

2,180 true total · 6 on this page

blue planet foods inc
Matched recall reason

Recall reason · Blue Planet products that contain the two recalled Dakota Specialty Milling ingredients; distribution of recalled bulk, wholesale, and …

Represented date
February 19, 2013
Product type
Food
Classification
Class II
Matching products
7
genesis partnership company sa
Matched product description

Product description · … Oz. (472 mL) bottle, Made in Guatemala, Distributed by Central Med Distribution, 6100 Hollywood Blvd, Hollywood FL 33024 …

Represented date
September 11, 2020
Product type
Drug
Classification
Class II
Matching products
1
ultradent products inc
Matched product description

Product description · … PermaFlo contains H1¿m average particle size with narrow upper limit particle distribution.

Represented date
June 01, 2022
Product type
Device
Classification
Class II
Matching products
15
apotex corp
Matched recall reason

Recall reason · Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.

Represented date
June 14, 2007
Product type
Drug
Classification
Class II
Matching products
2
steris corporation
Matched recall reason

Recall reason · Product not approved for release for US distribution

Represented date
May 15, 2026
Product type
Device
Classification
Class II
Matching products
79

Field note

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