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

Result scope

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 · 7 on this page

Recall event

Event 71426

71426

Matched recall reason

Recall reason · Superpotent Drug: Product may not be uniformly blended resulting in non-uniform distribution of the active ingredient menthol.

Represented date: June 04, 2015
Product type: Drug
Classification: Class III
Matching products: 1

Recall event

Event 75948

75948

Matched recall reason

Recall reason · … Product was shipped to distribution centers instead of the sterilization facility due to an operations error by a …

Represented date: December 12, 2016
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 97304

97304

Matched recall reason

Recall reason · … Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the …

Represented date: July 24, 2025
Product type: Drug
Classification: Class III
Matching products: 1

Recall event

Event 81523

81523

Matched recall reason

Recall reason · Failed Stability Specifications: Out-of-Specification results obtained for particle size distribution during stability testing.

Represented date: November 06, 2018
Product type: Drug
Classification: Class III
Matching products: 1

Recall event

Event 78811

78811

Matched recall reason

Recall reason · … together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.

Represented date: December 22, 2017
Product type: Drug
Classification: Class II
Matching products: 1

Recall event

Event 64011

64011

Matched product description

Product description · … Only approved for distribution from Authorized Distributors/Retailers, pharmaceutical laboratories and governmental research facilities.

Represented date: January 02, 2013
Product type: Food
Classification: Class II
Matching products: 1

Recall event

Event 82998

82998

Matched product description

Product description · Centricity PACS Foundation Centricity PACS software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution …

Represented date: May 16, 2019
Product type: Device
Classification: Class II
Matching products: 2

Products

24,938 true total · 11 on this page

Recalled product

Dr Blue Pain Relieving Gel, (4.6% menthol), For temporary relief of minor aches and pains of muscles and joints, a) 2 oz. Tube, NDC 10578-035-05, b) 5 oz. Jar, NDC 10578-035-04, Manufactured by Indiana Botanic Gardens, Hobart, IN 46342

D-1149-2015

Matched recall reason

Recall reason · Superpotent Drug: Product may not be uniformly blended resulting in non-uniform distribution of the active ingredient menthol.

Represented date: June 04, 2015
Product type: Drug
Classification: Class III

Recalled product

Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)

Z-0717-2022

Matched recall reason

Recall reason · … Rapid Test Kit) are not authorized, cleared, or approved for marketing and/or distribution in the U.S.

Represented date: January 13, 2022
Product type: Device
Classification: Class I

Recalled product

Medline E-Z Lubricating Jelly; Bacteriostatic. Water Soluble. Sterile. 2 FL OZ (59 ml). Product Usage: For medical purposes to lubricate body orifices to facilitate entry of diagnostic or therapeutic devices. Single use only. Sterile if unopened, undamaged package.

Z-0984-2017

Matched recall reason

Recall reason · … Product was shipped to distribution centers instead of the sterilization facility due to an operations error by a …

Represented date: December 12, 2016
Product type: Device
Classification: Class II

Recalled product

Albuterol Sulfate, Inhalation Aerosol, 90 mcg, 200 metered Inhalations, NET CONTENT 6.7 g, Manufactured by: Cipla Ltd, Indore, SEZ, Pithampur, India; Manufactured for: Cipla USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-142-60.

D-0593-2025

Matched recall reason

Recall reason · … Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the …

Represented date: July 24, 2025
Product type: Drug
Classification: Class III

Recalled product

Megestrol Acetate Oral Suspension, USP 625 mg/5mL, 150 mL bottle, Rx only, Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487, Manufactured by: Pharmaceutics International Inc. Hunt Valley, MD 21031

D-0279-2019

Matched recall reason

Recall reason · Failed Stability Specifications: Out-of-Specification results obtained for particle size distribution during stability testing.

Represented date: November 06, 2018
Product type: Drug
Classification: Class III

Recalled product

Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber Pharmaceuticals. Inc. Piscataway, NJ 08854 By: HETERO, Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar-509 301, India. NDC 31722-708-30

D-0415-2018

Matched recall reason

Recall reason · … together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.

Represented date: December 22, 2017
Product type: Drug
Classification: Class II

Recalled product

Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 782127

Z-1865-2024

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

Growth Factor Complex 200 GFC 200, Dietary Supplement 2 Fl Oz, Manufactured for: Soto Supplements P.O. Box 75774 Colorado Springs, CO 80237, Instructions: Place drops under your tongue for 2 min then swallow. Do not eat or drink for 15 min. Only approved for distribution from Authorized Distributors/Retailers, pharmaceutical laboratories and governmental research facilities.

F-0937-2013

Matched product description

Product description · … Only approved for distribution from Authorized Distributors/Retailers, pharmaceutical laboratories and governmental research facilities.

Represented date: January 02, 2013
Product type: Food
Classification: Class II

Recalled product

MR RT - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781439

Z-1858-2024

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

Centricity PACS Foundation Centricity PACS software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution, printing, editing, and processing of digital images and data acquired from diagnostic imaging devices.

Z-1911-2019

Matched product description

Product description · Centricity PACS Foundation Centricity PACS software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution …

Represented date: May 16, 2019
Product type: Device
Classification: Class II

Recalled product

MR RT Upgrades- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781440

Z-1859-2024

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

Firms

2,180 true total · 7 on this page

Firm

Indiana Botanic Gardens, Inc

indiana botanic gardens inc

Matched recall reason

Recall reason · Superpotent Drug: Product may not be uniformly blended resulting in non-uniform distribution of the active ingredient menthol.

Represented date: June 04, 2015
Product type: Drug
Classification: Class III
Matching products: 1

Firm

MEDLINE IND

medline ind

Matched recall reason

Recall reason · … Product was shipped to distribution centers instead of the sterilization facility due to an operations error by a …

Represented date: December 12, 2016
Product type: Device
Classification: Class II
Matching products: 1

Firm

Cipla USA, Inc.

cipla usa inc

Matched recall reason

Recall reason · … Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the …

Represented date: July 24, 2025
Product type: Drug
Classification: Class III
Matching products: 1

Firm

Breckenridge Pharmaceutical, Inc

breckenridge pharmaceutical inc

Matched recall reason

Recall reason · Failed Stability Specifications: Out-of-Specification results obtained for particle size distribution during stability testing.

Represented date: November 06, 2018
Product type: Drug
Classification: Class III
Matching products: 1

FDA name variants: Breckenridge Pharmaceutical, Inc · Breckenridge Pharmaceutical, Inc.

Firm

Hetero Labs Limited Unit V

hetero labs limited unit v

Matched recall reason

Recall reason · … together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.

Represented date: December 22, 2017
Product type: Drug
Classification: Class II
Matching products: 1

FDA name variants: Hetero Labs Limited Unit V · Hetero Labs Limited (Unit V)

Firm

EonNutra, LLC

eonnutra llc

Matched product description

Product description · … Only approved for distribution from Authorized Distributors/Retailers, pharmaceutical laboratories and governmental research facilities.

Represented date: January 02, 2013
Product type: Food
Classification: Class II
Matching products: 1

Firm

GE Healthcare, LLC

ge healthcare llc

Matched product description

Product description · Centricity PACS Foundation Centricity PACS software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution …

Represented date: February 27, 2026
Product type: Device
Classification: Class II
Matching products: 296

FDA name variants: GE Healthcare, LLC · GE Healthcare LLC