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 · 5 on this page

Recall event

Event 63995

63995

Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

Represented date: December 21, 2012
Product type: Food
Classification: Class II
Matching products: 2

Recall event

Event 64919

64919

Matched recalling firm

Recalling firm · Owens & Minor Distribution, Inc.

Represented date: March 26, 2013
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 63379

63379

Matched product description

Product description · Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The …

Represented date: October 03, 2012
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 73876

73876

Matched recalling firm

Recalling firm · Platinum Distribution Inc

Represented date: April 01, 2016
Product type: Food
Classification: Class I
Matching products: 1

Recall event

Event 91672

91672

Matched product description

Product description · … Adusa Distribution, LLC, Salisbury, NC 28147. NDC 72476-847-22

Represented date: February 09, 2023
Product type: Drug
Classification: Class II
Matching products: 2

Products

24,938 true total · 16 on this page

Recalled product

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

F-0883-2013

Matched recalling firm

Recalling firm · Dollar Tree Distribution, Inc.

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

Recalled product

Peptic Ulcer Test (H, pylori)

Z-0794-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Alcohol (ALC) Test Saliva

Z-0727-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Mycoplasma test, IgG and IgM

Z-0746-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

3 in 1 STI Test

Z-0817-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

H pylori (Peptic ulcer) Test

Z-0739-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Drug Test Small (4 substances)

Z-0734-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

MediChoice¿ Rayon Tipped OB/GYN Applicator, 8 inch, Plastic Shaft, Non-Sterile, Item Numbers WOD5001 and WOD5002. Product Usage: Usage: An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.

Z-1192-2013

Matched recalling firm

Recalling firm · Owens & Minor Distribution, Inc.

Represented date: March 26, 2013
Product type: Device
Classification: Class II

Recalled product

Herpes (HSV-1 & HSV-2) Test

Z-0740-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

8 in 1 STI Test Kit

Z-0818-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

2 in 1 Trichomonas / Gardnerella Test

Z-0816-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The device are Fluid Transfer Tube Sets, Sterile/EO, Std Volume Trifurcated, BAXA Corporation, Englewood, CO. The Repeater Pump is a device that provides a peristaltic pump driven fluid transfer that facilitates repeatable drug dosage distribution and reconstitution in hospital pharmacies. The device is for use with IV bags, syringes, elastomeric infusers, and other drug administration containers.

Z-0156-2013

Matched product description

Product description · Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The …

Represented date: October 03, 2012
Product type: Device
Classification: Class II

Recalled product

R No Sugar Added; Dark Chocolate 34 g/1.2 oz. Ross Chocolates, 4061 Butters Road, Scotch Creek, BC UPC 726007100054 Best Before: 191018

F-1588-2016

Matched recalling firm

Recalling firm · Platinum Distribution Inc

Represented date: April 01, 2016
Product type: Food
Classification: Class I

Recalled product

Epstein-Barr Virus (EBV VCA & EBNA IgG) Test

Z-0735-2026

Matched recall reason

Recall reason · Distribution without premarket approval/clearance.

Represented date: November 03, 2025
Product type: Device
Classification: Class II

Recalled product

Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 15-count cartons, Distributed By: Adusa Distribution, LLC, Salisbury, NC 28147. NDC 72476-847-22

D-0902-2023

Matched product description

Product description · … Adusa Distribution, LLC, Salisbury, NC 28147. NDC 72476-847-22

Represented date: February 09, 2023
Product type: Drug
Classification: Class II

Recalled product

Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT, STAY FREE SUPER 24/6CT, TAMPAX REG. 10CT, TAMPAX SUPER 10CT.

Z-1182-2026

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

Owens & Minor Distribution, Inc.

owens minor distribution inc

Matched recalling firm

Recalling firm · Owens & Minor Distribution, Inc.

Represented date: October 31, 2016
Product type: Device
Classification: Class II
Matching products: 5

Firm

Baxa Corporation

baxa corporation

Matched product description

Product description · Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The …

Represented date: June 04, 2013
Product type: Device
Classification: Class II
Matching products: 2

Firm

Platinum Distribution Inc

platinum distribution inc

Matched recalling firm

Recalling firm · Platinum Distribution Inc

Represented date: April 01, 2016
Product type: Food
Classification: Class I
Matching products: 1

Firm

L. Perrigo Company

l perrigo company

Matched product description

Product description · … Adusa Distribution, LLC, Salisbury, NC 28147. NDC 72476-847-22

Represented date: February 09, 2023
Product type: Drug
Classification: Class II
Matching products: 2