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 11 critical, 37 moderate, and 2 lower-severity recalls. The page references 34 distinct recalling firms operating in 5 distinct product categories, with 38 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), NHTSA (12), CPSC (2), 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 Devices Moderate Sep 24, 2014

BD Vacutainer EDTA Tubes (LAVENDER TOP TUBE 2.0ML) Part Number: BD 367841 Part Number: FMC 87-7841-7 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use.

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Sep 24, 2014

ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m) leadwires Part number: 8900-4052 These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFE's are processed through Gamma Radiation The indications for use include defibrillation, cardioversion, external non-invasive pacing and monitoring.

Bio-Detek, Inc.

FDA Devices Moderate Sep 24, 2014

BD Vacutainer Trace Element Tubes (ROYAL BLUE TOP TUBE 6.0ML) Part Number: 363083 Part Number: FMC 87-8380-1 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use. Trace elements, aluminum and zinc determination.

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Sep 24, 2014

Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, and ZZ98774. Designed for use within an institutional healthcare environment (i.e. assisted living, skilled nursing, transitional care, rehabilitation centers, etc.).

GF Health Products, Inc./d.b.a.Basic American Metal Products

FDA Devices Moderate Sep 24, 2014

Volcano TrakBack II Disposable Pullback Device; Sterile and nonpyrogenic; Single Use. TrakBack II is used to move the catheter steadily and precisely, allowing uniform collection of imaging data.

Volcano Corporation

FDA Devices Moderate Sep 24, 2014

The Brilliance CT Big Bore is a whole-body Computed Tomography X-ray system intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data from the same axial plane taken at different angles. Model Numbers 728244 and 728243.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Sep 24, 2014

ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry Systems, REF/Catalog Number/Siemens Material Number (SMN) 10491408, IVD ADVIA Chemistry A1c_3 Calibrator Information: For in vitro diagnostic use in the calibration of A1c_3 (A1c_3 and A1c_3M) and Total Hemoglobin_3 (tHb_3 and tHb_3M) methods on ADVIA Chemistry systems. The ADVIA Chemistry systems are automated, clinical chemistry analyzers that can run tests on human serum, plasma, or urine in random access and batch

Siemens Healthcare Diagnostics

FDA Devices Moderate Sep 24, 2014

Photonica Light Modulator. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed, UltraBlue, Slim-PRO, Dazzle Light, UltraSlim Cold Light, SlenderRay, and U-Slim It, as well as those products with private labelling branding. Company claims that the product provide non-invasive solutions to improve the appearance of fat accumulations, cellulite, fine lines, wrinkles, skin tone, and blemishes.

Advanced Photonic Systems, LLC

FDA Devices Moderate Sep 24, 2014

BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance to vancomycin and to predict the synergistic activity of this antimicrobial with an aminoglycoside antimicrobial.

Becton Dickinson & Co.

FDA Devices Moderate Sep 24, 2014

C-Series High Energy Linear Accelerator - Models: Novalis Tx, Trilogy, Trilogy Tx, Clinac iX, Clinac 2100 C/D, Clinac 2300C/D, Clinac 21EX, Clinac 23EX with versions 7, 8, 9 and 6 MV configuration and maximum dose rate of at least 6000 MU/min only. Varian High Energy Linear Accelerator is intended to provide sterotactic radiosurgery and precision radio-therapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.

Varian Medical Systems, Inc.

FDA Devices Moderate Sep 24, 2014

Luxurian. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed, UltraBlue, Slim-PRO, Dazzle Light, UltraSlim Cold Light, SlenderRay, and U-Slim It, as well as those products with private labelling branding. Company claims that the product provide non-invasive solutions to improve the appearance of fat accumulations, cellulite, fine lines, wrinkles, skin tone, and blemishes.

Advanced Photonic Systems, LLC

FDA Devices Low Sep 24, 2014

JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is a portable thermocycler and real-time fluorimeter capable of simultaneous and rapid identification of multiple biological warfare and clinical pathogens from a variety of biological specimens. The software and instrument provides an integrated environment for performing the required functions to control JBAIDS instruments and to perform PCR tests and analysis.

Biofire Defense

FDA Devices Moderate Sep 24, 2014

BD Vacutainer SST Tubes (RED/GREY TOP SST TUBE 3.5ML) Part Number: BD 367981 Part Number: 87-7981-5 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use. serum determination in chemistry.

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Sep 24, 2014

Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.

Amerx Health Care Corp.

FDA Devices Moderate Sep 24, 2014

ZOLL Pro-padz Sterile Adult Multi-Function Electrodes Part number: 8900-4012 These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFE's are processed through Gamma Radiation to a SAL of 1 o.e per International/ National Standards, EN ISO 11137- 2:2012 and ANSI/AAMI/ISO 11137-2:2013, Method 1, for use in a sterile environment by trained medical professionals. The indications for use include defibrillation, cardioversion, external n

Bio-Detek, Inc.

FDA Devices Moderate Sep 24, 2014

AXIOM Luminos dRF system with SW VD10 or on Luminos dRF Max The Axiom Luminos dRF is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. The Axiom Luminos dRF is a device intended to visualize anatomical structures by converting a pattern of X-ray into a visible image.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 24, 2014

BD Vacutainer Serum Tubes (RED TOP PLAIN TUBE 6.0 ML)Part Number: BD 367815 FMC Part Number: 87-7815-4 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use.

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Sep 24, 2014

Coulter DxH Diluent, Catalog No. 628017 Blood cell analysis comprises diluting a whole-blood sample with a solution that functions as a diluent. The diluent provides the ability to analyze portions of the diluted blood sample for different blood cell types and the measurement of hemoglobin.

Beckman Coulter Inc.

FDA Devices Moderate Sep 24, 2014

Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm); LW0057 (20gx57mm), LW0077(20gx77mm), LW0107(20gx107mm), LW0137(20gx137mm). The Bard DuaLok Breast Lesion Localization Wire is intended for use as a guide for directing surgical biopsies.

Bard Peripheral Vascular Inc

FDA Devices Moderate Sep 24, 2014

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 24, 2014

Tenor is a mobile passive lift, intended to be used on horizontal surfaces for lifting and transfer in hospitals, nursing homes or other healthcare facilities. Transfers with the Tenor are made indoors in the patient's room, in communal areas or in a bathroom. Tenor is meant to be used with the patient type who: sits in a wheelchair, has no capability to support themselves at all, cannot stand unsupported and is not able to bear weight (not even partially), is dependent on caregiver in most situ

ARJOHUNTLEIGH POLSKA SP. ZO.O.

FDA Devices Moderate Sep 24, 2014

ADVIA Centaur Immunoassay System, Catalog Numbers/Siemens Material Numbers (SMN) 10284980, 10286140, 10309524, 10309525, 10310210, 10313282, 10314322, 10316248, 10316372, 10316968, 10317060, 10317403, 10319111, 10319433, 10320929, 10321568, 10322149, 10322731, 10323204, 10325015, 10326217, 10327008, 10327379, 10328250, 10328647, 10329364, 10330873, 10331013, 10332617, 10334139, 10334759, 10337512, 10337526, 10339677, 10340551, 10340737, 10341051, 10341110, 10361010, 10361011, 10361012 --- For in

Siemens Healthcare Diagnostics

FDA Devices Moderate Sep 24, 2014

B.Braun Accuflo 100ML/H 100ML Elastomeric Infusion Device. AccuFlo devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications.

B. Braun Medical, Inc.

FDA Devices Moderate Sep 24, 2014

SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.

JK Products & Services, Inc

FDA Devices Low Sep 24, 2014

Stago IVD, Liquid Anti-Xa, NDC 3607450003116. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite Analyzers for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparins by measuring their anti-Xa activity on antithrombin in a competitive assay using a synthetic chromogenic substrate.

Diagnostica Stago, Inc.

FDA Devices Moderate Sep 24, 2014

Rusch, Soft Rubber (Nelaton and Nelaton Robinson), Bladder Catheter, Sterile. These catheters are indicated for the routine drainage of urine from the bladder. These catheters are not intended or designed for indwelling use.

Teleflex Medical

FDA Devices Moderate Sep 24, 2014

Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing, Amerigel Wound Wash, 22x2 Gauze Pads, and 1x3 Fabric Bandages CAT # A2002. Wound management.

Amerx Health Care Corp.

FDA Devices Moderate Sep 24, 2014

VERO Linear Accelerator System, Model Number MHI-TM2000; Common Name: Medical Linear Accelerator. MHI-TM2000 Linear Accelerator System is intended for radiation therapy of lesions, tumors and conditions anywhere in the body where radiation treatment is indicated.

MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK

FDA Devices Moderate Sep 24, 2014

Vac-Assist Suction Units (SUA01 Suction Aspirator Unit w/800 cc Canister). The suction unit is intended for professional use to remove fluids from a patient's airway or respiratory support unit. The intended population for this device is s both adult and pediatric.

EMG Technology Co., Ltd.

FDA Devices Moderate Sep 24, 2014

The Brilliance 64 and Ingenuity CT are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient, and equipment supports, components and accessories.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Sep 24, 2014

ZOLL Pro-padz Sterile Adult Multi-Function Electrodes ((singles) Part number: 8900-4013 These MFE Electrodes are used in connection with ZOLL Defibrillators for Adult patients. These disposable single use MFE's are processed through Gamma Radiation to a SAL of 1 o.e per International/ National Standards, EN ISO 11137- 2:2012 and ANSI/AAMI/ISO 11137-2:2013, Method 1, for use in a sterile environment by trained medical professionals. The indications for use include defibrillation, cardioversi

Bio-Detek, Inc.

FDA Devices Moderate Sep 24, 2014

Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion.

Genesis BPS, LLC.

FDA Devices Moderate Sep 24, 2014

Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion

Genesis BPS, LLC.

FDA Devices Moderate Sep 24, 2014

4D Integrated Treatment Console (4DITC), versions 10 and 11. 4DITC provided assistance for accurate treatment delivery by monitoring linear accelerator parameters and preventing the radiation therapy device from commencing irradiation when any parameter is out of conformance with the treatment plan.

Varian Medical Systems, Inc.

NHTSA No agency class Sep 24, 2014

FORD 2006-2014: EQUIPMENT ADAPTIVE/MOBILITY

FORD

NHTSA No agency class Sep 24, 2014

CHEVROLET 2013-2015: LATCHES/LOCKS/LINKAGES:HOOD:LATCH

CHEVROLET

CPSC No agency class Sep 23, 2014

Hearth & Home Technologies Recalls Gas Fireplaces, Stoves, Inserts and Log Sets Due to Risk of Gas Leak and Fire Hazard

Hearth & Home Technologies, of Lakeville, Minn.

NHTSA No agency class Sep 23, 2014

FREIGHTLINER 2013: FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY

FREIGHTLINER

NHTSA No agency class Sep 23, 2014

FREIGHTLINER 2014-2015: EQUIPMENT:ELECTRICAL

FREIGHTLINER

NHTSA No agency class Sep 23, 2014

FORD 2007-2014: EQUIPMENT ADAPTIVE/MOBILITY

FORD

USDA FSIS Critical Sep 23, 2014

Indiana Firm Recalls Uncured Beef Corn Dogs Due To Possible Temperature Abuse

Monogram Frozen Foods

NHTSA No agency class Sep 22, 2014

INFINITI 2013-2015: ENGINE AND ENGINE COOLING:ENGINE

INFINITI

NHTSA No agency class Sep 22, 2014

INFINITI 2014: POWER TRAIN:AUTOMATIC TRANSMISSION

INFINITI

NHTSA No agency class Sep 22, 2014

INFINITI 2014: HYBRID PROPULSION SYSTEM

INFINITI

NHTSA No agency class Sep 19, 2014

SUBARU 2015: TRAILER HITCHES

SUBARU

NHTSA No agency class Sep 19, 2014

LEXUS,TOYOTA 2014-2015: FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS

LEXUS,TOYOTA

NHTSA No agency class Sep 19, 2014

CADILLAC,SAAB 2010-2015: SUSPENSION:REAR

CADILLAC,SAAB

NHTSA No agency class Sep 19, 2014

CHEVROLET 2015: AIR BAGS

CHEVROLET

CPSC No agency class Sep 18, 2014

Siemens Recalls Audible Fire Alarm Base Due to Risk of Injury

Beijing Siemens Cerberus Electronics Ltd., of China

FDA Food Moderate Sep 17, 2014

Roundy's Salsa Con Queso; NET WT; 16 OZ (1 LB) 454g; DISTRIBUTED BY Roundy's Milwakee, WI 53202. Distributed in cases of 12/16 W jars.

Durrset Amigos, Ltd.

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.