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 14 critical, 35 moderate, and 1 lower-severity recalls. The page references 34 distinct recalling firms operating in 4 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (40), NHTSA (5), USDA FSIS (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 Jul 9, 2014

Laceration Trays, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc., Arden, NC.

Medical Action Industries Inc

FDA Devices Moderate Jul 9, 2014

BD FACS Canto and associated Fluidics Cart Product Usage: Flow cytometer for use in In vitro Diagnostics.

BD Biosciences, Systems & Reagents

FDA Devices Moderate Jul 9, 2014

Insert for IRK for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Vision Troubleshooting Guide for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for use in capturing images of the retina and anterior segment of the eye. Distributed by Nidek, Inc, and Marco Opthalmic Inc. Manufactured by Nidek Co. Ltd, Japan.

Nidek Inc

FDA Devices Moderate Jul 9, 2014

EXACTAMIX 1200 Compounder, model numbers 1200-DY, 1200-DX, 1200-DYR and 1200-DXR; EM1200 DY Display, Replacement EM 1200 DY Display. EXACTAMIX 2400 Compounder model numbers 2400-DY, 2400-DX, 2400-DYR and 2400-DYX. Baxa Corporation. An automated pumping system that compounds multiple sterile ingredients into a finished solution in a single patient IV administration bag.

Baxter Healthcare Corp.

FDA Devices Moderate Jul 9, 2014

Cautery QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Mobilett XP and Mobilett XP Hybrid are radiographic systems designed for use in wards, intensive care, and premature birth-wards, pediatric and emergency departments, operating theatres as well as the central X-ray department.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 9, 2014

Vessel Sealer QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

ACUSON S Family Ultrasound Systems at software versions VC25D, VC30A and VC30B; (S2000, S3000 and S1000 systems) Siemens Medical Solutions USA, Inc. Ultrasound imaging systems.

Siemens Medical Solutions USA, Inc.

FDA Devices Moderate Jul 9, 2014

illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is designed to be used with illumigene Molecular Assays. The device incubates illumigene Test Devices and reads endpoint reactions.

Meridian Bioscience Inc

FDA Devices Moderate Jul 9, 2014

Single Site US Manuals and Single Site OUS Manuals for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model numbers: PP-5.75-90 PP-9-90 PP-5.75-90PL PP-9-90PL

ORIGIO, Inc

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 4. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming arm, part numbers 3.113.025 and 03.113.026. Surgical instrument for use with Low Bend Medial Distal Tibia Plate. Orthopedic.

Synthes, Inc.

FDA Devices Moderate Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Jul 9, 2014

Laceration Kit: W/Needles, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

Medical Action Industries Inc

FDA Devices Moderate Jul 9, 2014

Natural Rubber Latex QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Simplexa" Flu A/B & RSV Direct, Model Number: MOL2650. 510(k) K120413  Simplexa" Flu A/B & RSV Direct. The Focus Diagnostics Simplexa Flu A/B & RSV Direct assay is intended for use on the 3M Integrated Cycler instrument for the in vitro qualitative detection and differentiation of influenza A virus, influenza B virus, and respiratory syncytial virus (RSV) RNA in nasopharyngeal swabs (NPS) from human patients with signs and symptoms of respiratory tract infection in conjunction with cli

Focus Diagnostics Inc

FDA Devices Critical Jul 9, 2014

Medtronic Neurosurgery

FDA Devices Moderate Jul 9, 2014

Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221

Microline Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.

Baxter Healthcare Corp.

FDA Devices Low Jul 9, 2014

DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.

DeVilbiss Healthcare LLC

FDA Devices Critical Jul 9, 2014

Medtronic Neurosurgery

FDA Devices Moderate Jul 9, 2014

BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code 882454. Gamma camera for Single Photon Emission Computed Tomography (SPECT) Medical Device for imaging.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 9, 2014

Vessel Sealer Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533), SMN 10310370, and Ancillary Pack Catalog number 03302138 (124581), SMN 10378677. Used on the ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP platforms. For in vitro diagnostic use in the quantitative determination of total homocysteine (HCY) in serum or plasma.

Siemens Healthcare Diagnostics, Inc

FDA Devices Critical Jul 9, 2014

Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Catheter, Catalog No. 46916. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar subarachnoid (intrathecal) region.

Medtronic Neurosurgery

FDA Devices Moderate Jul 9, 2014

Endowrist Instrument and Accessory Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Control System.

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Port-A-Cath Tray, Stage One: Sterile Single Use, Stage Two: Clean Ready to Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

Medical Action Industries Inc

FDA Devices Moderate Jul 9, 2014

Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and storage and transport of biological specimens.

Global Cooling Inc

FDA Devices Moderate Jul 9, 2014

Atrium Express Dry Seal Chest Drain ATS Blood Recovery, Catalog Number: 4050-100N. Autotransfusion Apparatus.

Atrium Medical Corporation

FDA Devices Moderate Jul 9, 2014

syngo Lab Data Manager, SMN 10800057, 10803189, and 10804573.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jul 9, 2014

Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.

Blue Belt Technologies MN

FDA Devices Moderate Jul 9, 2014

The Claymount Harmony is a grid cabinet designed to accept a digital x-ray imaging receptor and stationary grid. It contains signaling electronics to indicate the presence of the grid and detector as well as detector orientation. It may be mounted to a wall stand or incorporated in a radiographic table. It is intended to be used in general radiographic applications as a component of a radiographic system.

Claymount Assembli

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 6. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

McKesson Medi-Pak, Laceration Trays with Cotton O.R. Towels, Sterile, Single Use, Latex Free, 20 Each per Case, Rx only, Distributed by: McKesson Medical Surgical, Inc., Richmond, VA 23228

Medical Action Industries Inc

FDA Devices Critical Jul 9, 2014

Medtronic Neurosurgery

FDA Devices Critical Jul 9, 2014

Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT5000, BVM700, CPRM1000, CPRM2000, CPRM3000, PRO-1900, PRO-1000, PRO-2000, SC7000, SC8000, SC8020, SC8120, SC9000, SS3200, VN2000, VN3000, VN4000, VN5000, VT1000 , VN2102, VN2002. Emergency manual resuscitator for the Pediatric Population.

Ventlab LLC

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 8. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.

Zimmer, Inc.

NHTSA No agency class Jul 8, 2014

HYUNDAI 2007-2012: ENGINE AND ENGINE COOLING:ENGINE

HYUNDAI

NHTSA No agency class Jul 8, 2014

TOYOTA 2014: POWER TRAIN:AUTOMATIC TRANSMISSION:GEAR POSITION INDICATION (PRNDL)

TOYOTA

NHTSA No agency class Jul 8, 2014

FORD 2011-2013: ENGINE AND ENGINE COOLING:ENGINE:GASOLINE

FORD

NHTSA No agency class Jul 7, 2014

VOLKSWAGEN 2015: STEERING

VOLKSWAGEN

USDA FSIS Critical Jul 4, 2014

Nevada Firm Recalls Chicken Products That Were Produced Without Fully Implementing a Ready-To-Eat HACCP Plan

Kanani Foods II, Inc.

CPSC No agency class Jul 3, 2014

Big Fireworks Recalls Mock Sword Fireworks Devices Due to Impact, Burn Hazards

American Eagle dba Big Fireworks, of Lansing, Mich.

NHTSA No agency class Jul 3, 2014

CHEVROLET,OLDSMOBILE,PONTIAC 2000-2008: ELECTRICAL SYSTEM:IGNITION

CHEVROLET,OLDSMOBILE,PONTIAC

USDA FSIS Critical Jul 3, 2014

Texas Firm Recalls Beef Products Due to Possible Foreign Matter Contamination

HEB Meat Plant

FDA Food Critical Jul 2, 2014

Navitas Naturals Organic Sprouted Chia Powder, 8 oz (227g) package; Omega Fatty Acids, Protein, dietary Fiber. UPC 858847000369; Navitas Naturals, Novato, CA 94949

Navitas, LLC., dba Navitas Naturals

FDA Food Critical Jul 2, 2014

California Grown Shelled Walnuts, Net Weight 12 oz (340g), UPC 69887507806 46 cases, 24 count, 12 oz packages.

Suntree LLC

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.