PlainRecalls

2014 Recall Year Insight

Federal agencies issued 7,659 product recalls indexed by PlainRecalls in calendar year 2014. That represents about 7.33% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 21.0 recalls per day across the FDA, CPSC, USDA FSIS, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 154 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2014.

On this page of 50 records, severity classification shows 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 15 distinct recalling firms operating in 4 distinct product categories, with 20 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Drug (34), FDA Devices (16), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2014 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Mar 12, 2014

Teva Ethambutol Hydrochloride Tablets, USP, 400 mg, 100- count bottle, Rx Only,Distributed by Teva Pharmaceuticals, USA, Sellersville, PA., NDC 0555-0923-02.

Teva Pharmaceuticals USA

FDA Drug Moderate Mar 12, 2014

Teva Hydroxyzine Pamoate Capsules, USP, 25 mg, 100- count bottle, Rx Only,Distributed by Teva Pharmaceuticals, USA, Sellersville, PA. NDC 0555-0323-02.

Teva Pharmaceuticals USA

FDA Drug Moderate Mar 12, 2014

Triamcinolone Acetonide 3mg/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Tacrolimus (H20-based) 0.03% ophth.

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Voriconazole 1% opthal

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Cyanocobalamin 100mcg/ml injection

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Cyano B-12 p-f 1000mcg/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Sodium Bicarbonate 8.4% inj.

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Cyano B-12 (Cmpd) 1000mcg/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Hydroxyprogesterone Caproate

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Tetracaine 0.5% ophth.

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Voriconazole 0.5mg/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Lidocaine 4% Urethral Gel

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Dexamethasone phosphate 24mg/ml inj.

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Glutathione Inhalation 200mg/5ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Testosterone Cypionate 200mg/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Estradiol Cypionate 2mg/cc testosterone cypionoate 50mg

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Prostaglandin all combinations

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Bladder Instillation

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Testosterone Cypionate 100mg/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Hydroxocobalamin inj.

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

5-Fluorouracil 1% ophthal

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Vancomycin (fortified) 25mg/ml opth

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

AMP/M-B12/Pyridox/Methionine Inositol

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Vitamin D (Ergocalciferol) 800 u/ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Glutathione 6%/ascorbic 1%/DMSO 6.25%

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-Dose Vial, Rx only, NDC 63323-540-11, 25 vials in tray, each boxed vial individually labeled as: Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-Dose Vial, Rx only, NDC 63323-540-11.

Fresenius Kabi USA, LLC

FDA Drug Moderate Mar 12, 2014

Renacidin Irrigation

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

L-Glutathione inhalation

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Glutathione 1.25%/Ascorbic 1.25%/DMSO 6.25%

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Acetylcysteine 10% ophthalmic

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Terbutaline/Ipratropium 0.5mg/2.5ml

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Gentamycin 80mg/1000cc 0.9% NS

Natures Pharmacy & Compounding Center

FDA Drug Moderate Mar 12, 2014

Idoxuridine 0.1% Ophthalmic

Natures Pharmacy & Compounding Center

FDA Devices Moderate Mar 12, 2014

PRE1001US: Prevena Peel and Place System Kit (US-ONLY) Product Usage: The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.

KCI USA, INC.

FDA Devices Moderate Mar 12, 2014

Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's Robotic Arm Interactive Orthopedic System (RIO). It is composed of a unicompartmental implant system (Restoris MCK Uni) and a patellofemoral implant system (Restoris MCK PF). The Restoris MCK Uni is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees. In Restoris MCK combination where multi-compartmental areas are being treated, the Restoris MCK components wer

Mako Surgical Corporation

FDA Devices Moderate Mar 12, 2014

FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell to replicate the kinematics of a natural hip.

Djo Surgical

FDA Devices Moderate Mar 12, 2014

PRE1055: Prevena Dressing, 5 Pack Product Usage: The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.

KCI USA, INC.

FDA Devices Moderate Mar 12, 2014

Agility. Version 3.0 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators which is associated with Agility collimators.

Elekta, Inc.

FDA Devices Moderate Mar 12, 2014

Model Kodak 2100 Intraoral X-Ray System, Catalog Numbers 5303144, 8011579 -- Carestream Health, Inc. 150 Verona Street Rochester, NY 14608 -- Made in France -- TROPHY 77435 Marne La Vallee --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray, Extraoral with timer --- There are four major components: x-ray tube, x-ray generator, collimator and image receptor. These systems are permanently installed diagnostic dental x-ray systems for generation of x-rays for examin

Carestream Health Inc.

FDA Devices Moderate Mar 12, 2014

DeRoyal ST. Circumcision Clamp, REF 32-1622, Size 1.3 cm, 1 Per Pack, Rx Only STERILE EO, distributed by DeRoyal Industries.

DeRoyal Industries Inc

FDA Devices Moderate Mar 12, 2014

Desktop Pro TM linear accelerator control software intended to assist a licensed practitioner in the delivery of radiation to defined target volumes.

Elekta, Inc.

FDA Devices Moderate Mar 12, 2014

TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System.

Toshiba American Medical Systems Inc

FDA Devices Moderate Mar 12, 2014

Model Kodak 2200 Intraoral X-Ray System, Catalog Numbers 5303177, 5303169, 5303151, XR-5154323 -- Carestream Health, Inc. Made in France -- --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray, Extraoral with timer --- There are four major components: x-ray tube, x-ray generator, collimator and image receptor. These systems are permanently installed diagnostic dental x-ray systems for generation of x-rays for examination of the teeth, jaw and oral structures.

Carestream Health Inc.

FDA Devices Moderate Mar 12, 2014

Integrity. Version 1.1 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators.

Elekta, Inc.

FDA Devices Moderate Mar 12, 2014

Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027 and BI-700-00028 The 0-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D and 3D information of anatomic structures and objects with high x-ray attenuation such as bony anatomy and metallic objects. The 0-ann Imaging System is compatible with certain Image Guided Surgery Systems.

Medtronic Navigation, Inc.

FDA Devices Moderate Mar 12, 2014

Punch Hair Matic A surgical hair transplant device designed for automation of follicular transplantation.

MEDICAMAT S.A.

FDA Devices Moderate Mar 12, 2014

GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On- Alarm (AVOA) feature enabled. The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is intended for use under the direct supervision of a licensed healthcare practitioner, or by personnel trained in proper use of the equipment in a professional medical facility, such as hospital, clinic, surgical center or doctor's office. It can be used in multip

GE Healthcare, LLC

FDA Devices Moderate Mar 12, 2014

MEDITECH Microbiology - Calculator/data processing module, for clinical use.

Medical Information Technology, Inc.

FDA Devices Moderate Mar 12, 2014

*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch with 210 Micron Filter Pump, Prepierced Injection Site and Secure Lock; Made in Costa Rica; Product Inquiries should be directed to Hospira, Inc., Lake Forest, IL 60045 USA; *** 2) List Number 127200465 labeled in part: 12720-65 LifeShield LATEX-FREE HEMA; BLOOD SET, Nonvented, 81 Inch with 170 Micron Filter, Pump, Prepierced Injection Site and Secure Lock; Made in Costa Ri

Hospira Inc.

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2014 with 2013 →

Data Sources

  • Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
  • Source: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2014

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2014 across the FDA, CPSC, USDA FSIS and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of September 2026.