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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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 96891

96891

Matched product description

Product description · Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev …

Represented date: May 15, 2025
Product type: Device
Classification: Class I
Matching products: 1

Recall event

Event 99217

99217

Matched recall reason

Recall reason · … Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Represented date: June 11, 2026
Product type: Drug
Classification: Class II
Matching products: 10

Recall event

Event 64907

64907

Matched product description

Product description · … Each product is produced for a specific customer with their distribution information on the label. A general label …

Represented date: April 15, 2013
Product type: Food
Classification: Class III
Matching products: 1

Recall event

Event 89939

89939

Matched recall reason

Recall reason · … relevant 510(k) exemption and so their performance characteristics were not evaluated by the FDA prior to distribution.

Represented date: March 23, 2022
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 89524

89524

Matched recall reason

Recall reason · Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.

Represented date: January 14, 2022
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 88384

88384

Matched product description

Product description · … 7 60236 18732 5; Made in the Czech Republic, Distributed by Meijer Distribution Inc, Grand Rapids, MI 49544.

Represented date: July 27, 2021
Product type: Drug
Classification: Class II
Matching products: 1

Recall event

Event 85893

85893

Matched product description

Product description · … For Distribution exclusively by Gordon Food Service Wyoming, MI 49509

Represented date: June 18, 2020
Product type: Food
Classification: Class I
Matching products: 1

Products

24,938 true total · 12 on this page

Recalled product

Ingenia Elition X- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781358

Z-1852-2024

Matched recall reason

Recall reason · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may …

Represented date: May 03, 2024
Product type: Device
Classification: Class II

Recalled product

Achieva 3.0T for PET -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 781477

Z-1840-2024

Matched recall reason

Recall reason · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may …

Represented date: May 03, 2024
Product type: Device
Classification: Class II

Recalled product

Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.

Z-1904-2025

Matched product description

Product description · Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev …

Represented date: May 15, 2025
Product type: Device
Classification: Class I

Recalled product

Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.

Z-2761-2016

Matched recall reason

Recall reason · Nylon Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging.

Represented date: August 05, 2016
Product type: Device
Classification: Class II

Recalled product

SmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 782118

Z-1863-2024

Matched recall reason

Recall reason · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may …

Represented date: May 03, 2024
Product type: Device
Classification: Class II

Recalled product

Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781361

Z-1864-2024

Matched recall reason

Recall reason · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may …

Represented date: May 03, 2024
Product type: Device
Classification: Class II

Recalled product

BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) 100 x 10.5 mL Applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-34, catalog number 930700NS.

D-0652-2026

Matched recall reason

Recall reason · … Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Represented date: June 11, 2026
Product type: Drug
Classification: Class II

Recalled product

Free Form Amino Acids L-Arginine 7 L-Ornithine Complex With Alpha-Lipoic Acid, Promotes Circulation and Muscle Development, Dietary Supplement, 50 Vegetarian Capsules, Gluten Free, Serving Size 2 Capsules. Each product is produced for a specific customer with their distribution information on the label. A general label template was provided with attachment B information. Product is sold in 50 and 100 ct bottles.

F-1338-2013

Matched product description

Product description · … Each product is produced for a specific customer with their distribution information on the label. A general label …

Represented date: April 15, 2013
Product type: Food
Classification: Class III

Recalled product

TearCare version 1.0 SmartHubs

Z-1001-2022

Matched recall reason

Recall reason · … relevant 510(k) exemption and so their performance characteristics were not evaluated by the FDA prior to distribution.

Represented date: March 23, 2022
Product type: Device
Classification: Class II

Recalled product

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

Z-0723-2022

Matched recall reason

Recall reason · Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.

Represented date: January 14, 2022
Product type: Device
Classification: Class II

Recalled product

Meijer allergy relief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, NDC 41250-060-22 UPC 7 60236 18716 5; b) 30 count bottle, NDC 41250-060-39, UPC 7 60236 18717 2; c) 45 count bottle, NDC 41250-060-95, UPC 7 60236 18732 5; Made in the Czech Republic, Distributed by Meijer Distribution Inc, Grand Rapids, MI 49544.

D-0343-2022

Matched product description

Product description · … 7 60236 18732 5; Made in the Czech Republic, Distributed by Meijer Distribution Inc, Grand Rapids, MI 49544.

Represented date: July 27, 2021
Product type: Drug
Classification: Class II

Recalled product

Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution exclusively by Gordon Food Service Wyoming, MI 49509

F-1019-2020

Matched product description

Product description · … For Distribution exclusively by Gordon Food Service Wyoming, MI 49509

Represented date: June 18, 2020
Product type: Food
Classification: Class I

Firms

2,180 true total · 6 on this page

Firm

SunMed Holdings, LLC

sunmed holdings llc

Matched product description

Product description · Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev …

Represented date: December 15, 2025
Product type: Device
Classification: Class I
Matching products: 17

Firm

CareFusion 213, LLC

carefusion 213 llc

Matched recall reason

Recall reason · … Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Represented date: June 11, 2026
Product type: Drug
Classification: Class II
Matching products: 15

FDA name variants: CareFusion 213, LLC · Carefusion 213, Llc

Firm

Nexgen Pharma, Inc.

nexgen pharma inc

Matched product description

Product description · … Each product is produced for a specific customer with their distribution information on the label. A general label …

Represented date: November 19, 2013
Product type: Food
Classification: Class III
Matching products: 2

Firm

Sight Sciences, Inc.

sight sciences inc

Matched recall reason

Recall reason · … relevant 510(k) exemption and so their performance characteristics were not evaluated by the FDA prior to distribution.

Represented date: March 23, 2022
Product type: Device
Classification: Class II
Matching products: 1

Firm

Carl Zeiss Meditec, Inc.

carl zeiss meditec inc

Matched recall reason

Recall reason · Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.

Represented date: January 14, 2022
Product type: Device
Classification: Class II
Matching products: 9

Firm

Trident Seafoods Corporation

trident seafoods corporation

Matched product description

Product description · … For Distribution exclusively by Gordon Food Service Wyoming, MI 49509

Represented date: June 18, 2020
Product type: Food
Classification: Class I
Matching products: 1