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 · 3 on this page

Recall event

Event 67114

67114

Matched product description

Product description · … 2 mu, and 1 mu packages, For use and distribution in prescription compounding, manufacturing, processing or repacking only …

Represented date: October 21, 2013
Product type: Drug
Classification: Class I
Matching products: 1

Recall event

Event 88565

88565

Matched code information

Code information · UDI: (01)00884999042780(10)XXXXX(17)211015(240)04N02-021; US Distribution: Part Number 04N02-021, Lot Numbers …

Represented date: August 04, 2021
Product type: Device
Classification: Class II
Matching products: 1

Recall event

Event 68162

68162

Matched recall reason

Recall reason · … the external is not represented by contours, the bug can trigger an error in the 3D dose distribution.

Represented date: April 25, 2014
Product type: Device
Classification: Class II
Matching products: 1

Products

24,938 true total · 21 on this page

Recalled product

Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor. PN: 989803137631

Z-0908-2023

Matched recall reason

Recall reason · … Philips has decided to discontinue the distribution of this product.

Represented date: November 21, 2022
Product type: Device
Classification: Class II

Recalled product

STAR ActiveTrak Excimer Laser System, Model: STAR S3, Catalog Number: 0030-2450, Product is manufactured and distributed by AMO Manufacturing USA, LLC, Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive keratectomy (PRK), and phototherapeutic keratectomy (PTK) eye surgery in certain patient populations.

Z-0047-2014

Matched recall reason

Recall reason · … caused by an unexpected failure of a thyristor component on the AC Power Distribution Printed Circuit Board (PCB).

Represented date: September 16, 2013
Product type: Device
Classification: Class II

Recalled product

STAR Excimer Laser System, Model STAR S4 IR, Catalog Number: 0030-4864, Product is manufactured and distributed by AMO Manufacturing USA, LLC Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive keratectomy (PRK), and phototherapeutic keratectomy (PTK) eye surgery in certain patient populations.

Z-0049-2014

Matched recall reason

Recall reason · … caused by an unexpected failure of a thyristor component on the AC Power Distribution Printed Circuit Board (PCB).

Represented date: September 16, 2013
Product type: Device
Classification: Class II

Recalled product

BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol),500 x 1 mL applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31, bulk catalog number 930480NSB

D-0651-2026

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

Rugby Polyvitamin Liquid, 1 2/3 oz (50 mL)

F-3521-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Rugby Liquid Vitamin C Supplement, 4 oz., 118 mL

F-3519-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Major Ferrous Drops, 1 2/3 oz (50 mL)

F-3526-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Human Chorionic Gonadotropin, EP (HCG) in 5 mu. 2 mu, and 1 mu packages, For use and distribution in prescription compounding, manufacturing, processing or repacking only in accordance with FDA regulations and applicable law. Potency 5489.6IU/mg. Packed by Medisca, Inc. Irving, TX, 75063, USA NDC 38779-2673-1, NDC 38779-2673-2, and NDC 38779-2673-6. Lot Numbers 101751/A, Exp: 05/16, CAS: 9002-61-3; 101752/A, Exp: 05/16, CAS 9002-61-3; and 101799/A, Exp: 05/16, CAS: 9002-61-3

D-1263-2014

Matched product description

Product description · … 2 mu, and 1 mu packages, For use and distribution in prescription compounding, manufacturing, processing or repacking only …

Represented date: October 21, 2013
Product type: Drug
Classification: Class I

Recalled product

Vysis CLL FISH Probe Kit with the following components: Vysis LSI p53 SpectrumOrange/ATM, SpectrumGreen and LSI D13S319, SpectrumOrange/ 13q34, SpectrumAqua/CEP 12 SpectrumGreen Probes

Z-2576-2021

Matched code information

Code information · UDI: (01)00884999042780(10)XXXXX(17)211015(240)04N02-021; US Distribution: Part Number 04N02-021, Lot Numbers …

Represented date: August 04, 2021
Product type: Device
Classification: Class II

Recalled product

STAR Excimer Laser System with Variable Spot Scanning, Model: STAR S4, Catalog Number: 0030-4077, Product is manufactured and distributed by AMO Manufacturing USA, LLC, Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive keratectomy (PRK), and phototherapeutic keratectomy (PTK) eye surgery in certain patient populations.

Z-0048-2014

Matched recall reason

Recall reason · … caused by an unexpected failure of a thyristor component on the AC Power Distribution Printed Circuit Board (PCB).

Represented date: September 16, 2013
Product type: Device
Classification: Class II

Recalled product

Major Poly-Vita Drops, 1 2/3 oz (50 mL)

F-3527-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Major Tri-Vita Drops, 1 2/3 oz (50 mL)

F-3529-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Rugby Tri-vitamin Liquid, 1 2/3 oz (50 mL)

F-3523-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Major D-Vita Drops, 1 2/3 oz (50 mL)

F-3525-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL

F-3518-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Rugby Polyvitamin Liquid with Iron, 1 2/3 oz (50 mL)

F-3522-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the labels is TriMed Inc., Santa Clarita, CA.

Z-0359-2020

Matched distribution pattern

Distribution pattern · Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China …

Represented date: September 28, 2018
Product type: Device
Classification: Class II

Recalled product

RayStation software version 4.0.3.4 RayStation is a software system designed for treatment planning and analysis of radiation therapy.

Z-1806-2014

Matched recall reason

Recall reason · … the external is not represented by contours, the bug can trigger an error in the 3D dose distribution.

Represented date: April 25, 2014
Product type: Device
Classification: Class II

Recalled product

Major Poly-Vita Drops with Iron, 1 2/3 oz (50 mL)

F-3528-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Rugby D 3 Vitamin Liquid, 400 IUI/1 mL, 1 and 2/3 oz., 50 mL

F-3517-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Recalled product

Leader Liquid Multivitamin Supplement for Infants and Toddlers , 1 2/3 oz (50 mL)

F-3530-2017

Matched recall reason

Recall reason · The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating …

Represented date: August 02, 2017
Product type: Food
Classification: Class II

Firms

2,180 true total · 1 on this page

Firm

Abbott Molecular, Inc.

abbott molecular inc

Matched code information

Code information · UDI: (01)00884999042780(10)XXXXX(17)211015(240)04N02-021; US Distribution: Part Number 04N02-021, Lot Numbers …

Represented date: April 28, 2025
Product type: Device
Classification: Class II
Matching products: 18