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 · 9 on this page

Recall event

Event 80128

80128

Matched product description

Product description · … Poseidon Distribution Atlanta, GA, UPC 638632428857

Represented date: May 17, 2018
Product type: Drug
Classification: Class I
Matching products: 1

Recall event

Event 61830

61830

Matched product description

Product description · Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide

Represented date: October 19, 2011
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 74982

74982

Matched product description

Product description · … 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination …

Represented date: August 15, 2016
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 88427

88427

Matched recall reason

Recall reason · Product label intended for the European community was distributed to the USA market via their US distribution organization

Represented date: June 25, 2021
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 81483

81483

Matched product description

Product description · … by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.

Represented date: October 19, 2018
Product type: Drug
Classification: Class II
Matching products: 1

Recall event

Event 95223

95223

Matched recall reason

Recall reason · The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has …

Represented date: August 06, 2024
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 66978

66978

Matched recall reason

Recall reason · … various lots of Avex CX2 Orthodontic Brackets because the design control process was not complete prior to distribution.

Represented date: November 19, 2013
Product type: Device
Classification: Class III
Matching products: 1

Recall event

Event 87829

87829

Matched recall reason

Recall reason · Manufacturing failed to follow process steps resulting in the distribution of potentially defective devices

Represented date: February 02, 2021
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 72252

72252

Matched product description

Product description · UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.

Represented date: September 16, 2015
Product type: Drug
Classification: Class III
Matching products: 2

Products

24,938 true total · 10 on this page

Recalled product

POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857

D-0879-2018

Matched product description

Product description · … Poseidon Distribution Atlanta, GA, UPC 638632428857

Represented date: May 17, 2018
Product type: Drug
Classification: Class I

Recalled product

Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide

Z-1538-2012

Matched product description

Product description · Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide

Represented date: October 19, 2011
Product type: Device
Classification: Class II

Recalled product

BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group A streptococci and group D enterococci bacteria.

Z-1422-2013

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

Recalled product

Thermo Scientific QMS Everolimus Assay; Model number: 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination of Everolimus, in human whole blood on automated clinical chemistry analyzers. The results obtained are used as an aid in the management of kidney and liver transplant patients receiving Everolimus therapy. This in vitro diagnostic device is intended for clinical laboratory use only. The QMS Everolimus assay is intended to be used as an aid in the management of patients receiving everolimus therapy for those organ transplant procedures indicated in the chart for each specific country.

Z-0008-2017

Matched product description

Product description · … 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination …

Represented date: August 15, 2016
Product type: Device
Classification: Class II

Recalled product

KeyPrint Soft- bottle, 32.5 oz (1kg). Resin for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints and repositioners. Model (Ref) #: 4220005

Z-2336-2021

Matched recall reason

Recall reason · Product label intended for the European community was distributed to the USA market via their US distribution organization

Represented date: June 25, 2021
Product type: Device
Classification: Class II

Recalled product

Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.

D-0276-2019

Matched product description

Product description · … by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.

Represented date: October 19, 2018
Product type: Drug
Classification: Class II

Recalled product

General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Number: 102-S60C

Z-3154-2024

Matched recall reason

Recall reason · The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has …

Represented date: August 06, 2024
Product type: Device
Classification: Class II

Recalled product

Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex CX2 ceramic brackets are intended for use in orthodontic treatment.

Z-0481-2014

Matched recall reason

Recall reason · … various lots of Avex CX2 Orthodontic Brackets because the design control process was not complete prior to distribution.

Represented date: November 19, 2013
Product type: Device
Classification: Class III

Recalled product

IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06.59 - Product Usage: Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals.

Z-1671-2021

Matched recall reason

Recall reason · Manufacturing failed to follow process steps resulting in the distribution of potentially defective devices

Represented date: February 02, 2021
Product type: Device
Classification: Class II

Recalled product

UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.

D-0782-2016

Matched product description

Product description · UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.

Represented date: September 16, 2015
Product type: Drug
Classification: Class III

Firms

2,180 true total · 6 on this page

Firm

Shoreside Enterprises Inc.

shoreside enterprises inc

Matched product description

Product description · … Poseidon Distribution Atlanta, GA, UPC 638632428857

Represented date: May 17, 2018
Product type: Drug
Classification: Class I
Matching products: 1

Firm

Philips Healthcare Inc.

philips healthcare inc

Matched product description

Product description · Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide

Represented date: August 08, 2013
Product type: Device
Classification: Class II
Matching products: 30

Firm

Microgenics Corporation

microgenics corporation

Matched product description

Product description · … 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination …

Represented date: October 01, 2025
Product type: Device
Classification: Class II
Matching products: 8

Firm

Straumann USA LLC

straumann usa llc

Matched recall reason

Recall reason · Product label intended for the European community was distributed to the USA market via their US distribution organization

Represented date: March 17, 2026
Product type: Device
Classification: Class II
Matching products: 16

FDA name variants: Straumann USA LLC · Straumann USA, LLC

Firm

Taro Pharmaceuticals U.S.A., Inc.

taro pharmaceuticals u s a inc

Matched product description

Product description · … by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.

Represented date: October 19, 2018
Product type: Drug
Classification: Class II
Matching products: 1

Firm

Cypress Medical Products LLC

cypress medical products llc

Matched recall reason

Recall reason · The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has …

Represented date: August 20, 2024
Product type: Device
Classification: Class II
Matching products: 6