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

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

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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 · 6 on this page

Recall event

Event 88892

88892

Matched recall reason

Recall reason · Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.

Represented date: October 20, 2021
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 79262

79262

Matched recall reason

Recall reason · Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Represented date: December 04, 2017
Product type: Device
Classification: Class II
Matching products: 4

Recall event

Event 95826

95826

Matched product description

Product description · … 128 FL OZ (1 GAL) 3.785 L, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509

Represented date: November 06, 2024
Product type: Drug
Classification: Class II
Matching products: 1

Recall event

Event 93187

93187

Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date: October 05, 2023
Product type: Drug
Classification: Class II
Matching products: 1

Recall event

Event 99021

99021

Matched recall reason

Recall reason · Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Represented date: April 30, 2026
Product type: Device
Classification: Class II
Matching products: 4

Recall event

Event 94575

94575

Matched product description

Product description · … Meijer Distribution Inc., Grand Rapids,MI 49544, NDC 79481-0034-9

Represented date: May 01, 2024
Product type: Drug
Classification: Class II
Matching products: 1

Products

24,938 true total · 15 on this page

Recalled product

Candy Canes, Peppermint Flavor, 5 oz boxes, packed 12 individually candy canes/box, and labeled in part Distributed by Greenbriar International, Inc., Chesapeake, VA 23320, MADE IN CHINA

F-0882-2013

Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date: December 21, 2012
Product type: Food
Classification: Class II

Recalled product

Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, TROJAN CONDOMS MAGNUM 48 CT DISP, *BOX TROJAN CONDOMS MAGNUM 50CT .

Z-1181-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

Represented date: December 26, 2025
Product type: Device
Classification: Class II

Recalled product

Aspiration Syringe Kit, REF: MVSK60

Z-0202-2022

Matched recall reason

Recall reason · Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.

Represented date: October 20, 2021
Product type: Device
Classification: Class II

Recalled product

Truth Renew

Z-0820-2018

Matched recall reason

Recall reason · Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Represented date: December 04, 2017
Product type: Device
Classification: Class II

Recalled product

Ultra Renew

Z-0819-2018

Matched recall reason

Recall reason · Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Represented date: December 04, 2017
Product type: Device
Classification: Class II

Recalled product

Truth Renew Plus

Z-0822-2018

Matched recall reason

Recall reason · Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Represented date: December 04, 2017
Product type: Device
Classification: Class II

Recalled product

Ultra Renew Plus

Z-0821-2018

Matched recall reason

Recall reason · Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Represented date: December 04, 2017
Product type: Device
Classification: Class II

Recalled product

Array Liquid Antiseptic Handwash, Chloroxylenol 0.1%, NET CONTENTS: 128 FL OZ (1 GAL) 3.785 L, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509

D-0089-2025

Matched product description

Product description · … 128 FL OZ (1 GAL) 3.785 L, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509

Represented date: November 06, 2024
Product type: Drug
Classification: Class II

Recalled product

Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail stores.

D-0045-2024

Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date: October 05, 2023
Product type: Drug
Classification: Class II

Recalled product

UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.

D-1036-2020

Matched recalling firm

Recalling firm · Med Man Distribution, Inc.

Represented date: November 08, 2019
Product type: Drug
Classification: Class I

Recalled product

Halyard, Pain Pack. Kit Code: AMPK48-01.

Z-2407-2026

Matched recall reason

Recall reason · Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Represented date: April 30, 2026
Product type: Device
Classification: Class II

Recalled product

Halyard, Drape Pack. Kit Code: LMDP36-01.

Z-2409-2026

Matched recall reason

Recall reason · Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Represented date: April 30, 2026
Product type: Device
Classification: Class II

Recalled product

Halyard, Towel Six Pack. Kit Code: AMTS70-01.

Z-2408-2026

Matched recall reason

Recall reason · Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Represented date: April 30, 2026
Product type: Device
Classification: Class II

Recalled product

Halyard, Eye Bag Pack. Kit Code: UIEB48-01.

Z-2410-2026

Matched recall reason

Recall reason · Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Represented date: April 30, 2026
Product type: Device
Classification: Class II

Recalled product

Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free, Sugar Free Grape, 10 fl. oz bottle, Distributed by: Meijer Distribution Inc., Grand Rapids,MI 49544, NDC 79481-0034-9

D-0501-2024

Matched product description

Product description · … Meijer Distribution Inc., Grand Rapids,MI 49544, NDC 79481-0034-9

Represented date: May 01, 2024
Product type: Drug
Classification: Class II

Firms

2,180 true total · 4 on this page

Firm

Microvention, Inc.

microvention inc

Matched recall reason

Recall reason · Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.

Represented date: September 05, 2025
Product type: Device
Classification: Class II
Matching products: 10

FDA name variants: Microvention, Inc. · MICROVENTION INC.

Firm

Accord Media, LLC

accord media llc

Matched recall reason

Recall reason · Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Represented date: December 04, 2017
Product type: Device
Classification: Class II
Matching products: 4

Firm

Midlab Incorporated

midlab incorporated

Matched product description

Product description · … 128 FL OZ (1 GAL) 3.785 L, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509

Represented date: November 06, 2024
Product type: Drug
Classification: Class II
Matching products: 1

Firm

AVID Medical, Inc.

avid medical inc

Matched recall reason

Recall reason · Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Represented date: April 30, 2026
Product type: Device
Classification: Class II
Matching products: 86

FDA name variants: AVID Medical, Inc. · Avid Medical, Inc.