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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 · 5 on this page

Recall event

Event 98234

98234

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

Represented date: December 26, 2025
Product type: Device
Classification: Class II
Matching products: 5

Recall event

Event 85122

85122

Matched product description

Product description · … FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Distribution, 10 tests/box …

Represented date: February 21, 2020
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 75558

75558

Matched product description

Product description · SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of …

Represented date: October 28, 2016
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 84265

84265

Matched recalling firm

Recalling firm · Med Man Distribution, Inc.

Represented date: November 08, 2019
Product type: Drug
Classification: Class I
Matching products: 2

Recall event

Event 94261

94261

Matched recall reason

Recall reason · Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device …

Represented date: April 22, 2024
Product type: Device
Classification: Class II
Matching products: 5

Products

24,938 true total · 16 on this page

Recalled product

LUCKY ICE, Cool Mouthwash, Alcohol Free, 16.9oz, 12CT, UPC: 808829108989

D-0284-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

PREGNANCY TEST 24CT

Z-1184-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

AmniSure ROM Test, Material Nos. FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Distribution, 10 tests/box), FMRT-1-25-CA (Canadian Distribution; 25 tests/box)

Z-1636-2020

Matched product description

Product description · … FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Distribution, 10 tests/box …

Represented date: February 21, 2020
Product type: Device
Classification: Class II

Recalled product

Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148

D-0282-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

TUMS a) Assorted, 12 Ct.; b) Extra Strength (EX) Assorted Berries, 12-count #1194A 05/27; c)Extra Strength (EX) Assorted Fruit, 12-count, #1194C 03/27

D-0279-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

TYLENOL a) 500 MG., 2'S DISPLAY, 50CT; b) COLD & FLU, 25CT/2S; c) COLD & FLU SEVERE, 2PK, 50CT; d) PM, 50CT; e) SINUS SEVERE, 2PK, 50CT

D-0277-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932

D-0263-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

Dietary Supplements packaged in the following configurations: (1) No-Fenol Chewable, Multi-Enzyme Product for Digestion of Phenolic Foods and Fibers, packaged 180-chewable tablets bottles (SKU 54651). Firm name on the label is Houston Nutraceutical Inc. (HNI), Siloam, AR; (2) Bulk C613 Houston No-Fenol Bulk powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83451); (3) Bulk C613 Houston No-Fenol Chew T chewable tablets, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92566);

F-0806-2014

Matched product description

Product description · … within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83451); (3) Bulk C613 Houston …

Represented date: October 30, 2013
Product type: Food
Classification: Class II

Recalled product

Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559

D-0261-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Recalled product

Amy's Vegetable Lasagna, 9.5 oz (269 g) 12 boxes per case. UPC 0 42272 00032 6 - US Distribution: UPC 0-42272-90032-9 - Canadian distribution Vegetable Lasagna 8 pack - 9.5 oz, (269g) UPC: 0-42272-00032-6 - US distribution Family Size, 28 oz. (794 g), 8 boxes per case UPC 0-42272-00965-7 - US distribution Club size, 57 oz. 3.6 lbs, 1.6 kg, 6 x 9.5 oz, per case UPC: 0-42272-00201-6 Amy's Kitchen, Petaluma, CA 94953

F-2351-2015

Matched product description

Product description · … UPC 0 42272 00032 6 - US Distribution: UPC 0-42272-90032-9 - Canadian distribution Vegetable Lasagna 8 pack …

Represented date: March 22, 2015
Product type: Food
Classification: Class II

Recalled product

SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices. For uterine sound

Z-0655-2017

Matched product description

Product description · SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of …

Represented date: October 28, 2016
Product type: Device
Classification: Class II

Recalled product

Bow & Arrow, Dietary Supplement, Libido Enhancer for Men, a) Four pack, b) Ten pack capsules per carton, Exclusively Manufactured by: Medicine Man Distribution, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783

D-1037-2020

Matched recalling firm

Recalling firm · Med Man Distribution, Inc.

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

Recalled product

Streptococcal A rapid test kits, labeled as: Easy Healthcare Corporation, Areta Strep A Swab Test and EASY at Home Medical LLC, Areta One Step Strep A Swab Test, Part Number ARST-100

Z-2032-2024

Matched recall reason

Recall reason · Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device …

Represented date: April 22, 2024
Product type: Device
Classification: Class II

Recalled product

Amy's Vegetable Lasagna, Light in Sodium, 9.5 oz (269 g) 12 boxes per case. UPC: 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA

F-2360-2015

Matched product description

Product description · … 0-42272-00240-5, US distribution only; UPC : 0-42272-90807-3 - Canadian distribution Amy Kitchen, Petaluma, CA

Represented date: March 22, 2015
Product type: Food
Classification: Class II

Recalled product

Independent Medical Co-op Inc., Streptococcal A rapid test kits, labeled as: IMCO Strep A Rapid Test Strip and IMCO Strep A Rapid Test, Part Number STP25-IMC

Z-2033-2024

Matched recall reason

Recall reason · Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device …

Represented date: April 22, 2024
Product type: Device
Classification: Class II

Recalled product

Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT

Z-1180-2026

Matched recalling firm

Recalling firm · GOLD STAR DISTRIBUTION INC

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

Firms

2,180 true total · 4 on this page

Firm

Qiagen Sciences LLC

qiagen sciences llc

Matched product description

Product description · … FMRT-1-25-US (US Distribution, 25 tests/box), FMRT-1-10-US (US Distribution, 10 tests/box …

Represented date: April 28, 2023
Product type: Device
Classification: Class II
Matching products: 7

Firm

Hologic, Inc

hologic inc

Matched product description

Product description · SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of …

Represented date: April 08, 2026
Product type: Device
Classification: Class II
Matching products: 29

FDA name variants: Hologic, Inc · Hologic, Inc. · Hologic Inc

Firm

Med Man Distribution, Inc.

med man distribution inc

Matched recalling firm

Recalling firm · Med Man Distribution, Inc.

Represented date: November 08, 2019
Product type: Drug
Classification: Class I
Matching products: 2

Firm

Wondfo USA Co Ltd

wondfo usa co ltd

Matched recall reason

Recall reason · Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device …

Represented date: April 22, 2024
Product type: Device
Classification: Class II
Matching products: 5