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 15 critical, 33 moderate, and 2 lower-severity recalls. The page references 31 distinct recalling firms operating in 7 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), FDA Food (11), NHTSA (5), 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 Dec 3, 2014

8MM, DUAL BLADE RETRACTOR; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Latex Reagent, DR0802, Lot 1301912. The responsible firm on the label is Oxoid Ltd.

Remel Inc

FDA Devices Moderate Dec 3, 2014

8MM,MEDIUM-LARGE CLIP APPLIER ; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.

Abbott Molecular

FDA Devices Moderate Dec 3, 2014

Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product is composed of die-cut hydrocolloid-coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose of infants to provide a protective barrier to the philtrum, columella, septum, nares, and tip of nose. It is available in multiple sizes that vary the external geometry and nare hole size and

Beevers Manufacturing & Supply, Inc.

FDA Devices Moderate Dec 3, 2014

8MM, CURVED BIPOLAR DISSECTOR; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

Dharma Cavity Varnish 15mL

Dharma Research, Inc.

FDA Devices Moderate Dec 3, 2014

ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated microparticles in MES buffer with sheep IgG stabilizers. Minimum Concentration: 0.08% solids. Preservative: ProClin 300. - 1 or 4 Bottle(s) (5.9 mL/26.3 mL) T3 acridinium-labeled conjugate in citrate buffer with NaCl and Triton X-100 stabilizers. Minimum concentration: 0.33 ng/mL. Preservative: ProClin 300. The ARCHITECT Total T3 (TT3) assay is a chemiluminescent microparticle

Abbott Ireland Diagnostics Division

FDA Devices Moderate Dec 3, 2014

The J700 Floor Mounted Tube Stand (FMTS) is intended to support and position the diagnostic x-ray tube housing assembly for a medical radiographic procedure. The product consists of a vertical column (with counterbalanced vertical carriage, counterweight and pulley system), horizontal floor car and a floor mounted track to ride on.

Summit Industries Inc.

FDA Devices Moderate Dec 3, 2014

Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A The software is applicable to the following CT systems: Aquilion ONE TSX-301A/2D X-ray CT system with a 320-row 0.5 mm detector is provided with a 7.5-MHU large-capacity X-ray tube unit, and permits scanning over large areas at the high-speed of 0.35 s per rotation. The system features are; 160-mm-wide area detector, station, gantry and patient couch operation controls, image reconstruction, high-speed volume s

Toshiba American Medical Systems Inc

FDA Devices Moderate Dec 3, 2014

Oxoid Legionella Pneumo Groups 2-14 Latex Test, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, Lot 1301912. The product is a latex agglutination test for the identification of predominant Legionella species grown on plate media from patients with suspected Legionellosis or from environmental sources. The test allows a separate identification of Legionella pneumophila serogroup 15 and serogroups 1-14

Remel Inc

FDA Devices Moderate Dec 3, 2014

Instructions for Use for the blue endo MOREsolution Electromechanical Laparoscopic Morcellator System, Model 55-000011, consisting of the control unit, hand-grip, flexible shaft, trocars/obturators, sleeves, valves, and blades.

Market-Tiers Inc

FDA Devices Moderate Dec 3, 2014

Dharma Cavity Varnish with Fluoride

Dharma Research, Inc.

FDA Devices Moderate Dec 3, 2014

8MM,BLACK DIAMOND MICRO FORCEPS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

8MM,LARGE NEEDLE DRIVER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

8MM PERMANENT CAUTERY SPATULA,; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators are microprocessor-controlled, electrically powered mechanical ventilators. Intended for use by medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients.

Respironics California Inc

FDA Devices Low Dec 3, 2014

LUNA Chest, Model No. LU4006

Novadaq Technologies, Inc.

FDA Devices Moderate Dec 3, 2014

IntelliSpace Portal DX/HX/EX model number: 881001 IntelliSpace Portal DX/HX/EX Upgrade model number: 881011 IntelliSpace Portal DX/HX/EX Demo model number: 881012 IntelliSpace Portal IX model number; 881030 System, x-ray, tomography, computed

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Dec 3, 2014

8MM, SMALL GRASPING RETRACTOR ; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

8MM,PROGRASP FORCEPS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Low Dec 3, 2014

Non-sterile drape

Novadaq Technologies, Inc.

FDA Devices Moderate Dec 3, 2014

8MM FENESTRATED BIPOLAR FORCEPS,; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen device with two balloons mounted near the distal tip for the treatment of cerebral ischemia resulting from symptomatic vasospasm following aneurysmal subarachnoid hemorrhage. The NeuroFlo Catheter is under Humanitarian Device Exemption and not commercially released under a premarket notification or premarket approval.

ZOLL Circulation, Inc.

FDA Devices Moderate Dec 3, 2014

8MM, ATRIAL RETRACTOR SHORT RIGHT ; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Moderate Dec 3, 2014

Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial Impactor to impact the tibial tray onto the tibia.

Zimmer, Inc.

FDA Devices Moderate Dec 3, 2014

Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A The software is applicable to the following CT systems: Aquilion ONE TSX-301C X-ray CT system with a 320-row 0.5 mm detector is provided with a 7.5-MHU large-capacity X-ray tube unit, and permits scanning over large areas at the high-speed of 0.35 s per rotation. The system features are; 160-mm-wide area detector, station, gantry and patient couch operation controls, image reconstruction, high-speed volume scan, hi

Toshiba American Medical Systems Inc

FDA Devices Moderate Dec 3, 2014

Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Tibia) is intended to be used as a surgical instrument to assist in the positioning of Total Knee Replacement components intraoperatively and in guiding the marking of bone before cutting provided that anatomic landmarks necessary for alignment and positioning of the implant are identifiable on patient imaging scans.

Materialise USA LLC

FDA Devices Moderate Dec 3, 2014

8MM, LARGE HEM-O-LOK CLIP APPLIER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

FDA Devices Critical Dec 3, 2014

Gel-E Donut : 92025-A (Extra Small), 92025-B (Small), 92025-C (Medium) and Squishon 2 91033-2. The products are intended to support and cradle a baby's head and/or body.

Philips Medical Systems, Inc.

FDA Devices Moderate Dec 3, 2014

CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5 Model Number(s): R2010 Intended Use: Diagnosis and treatment of non-invasive HPV-related or unrelated lesions of the lower genital tract.

CooperSurgical, Inc.

NHTSA No agency class Dec 3, 2014

CHRYSLER,DODGE 2004-2005: AIR BAGS

CHRYSLER,DODGE

CPSC No agency class Dec 2, 2014

Daikin Recalls Air Purifiers Due to Fire Hazard

Daikin Industries Ltd, of Japan

CPSC No agency class Dec 2, 2014

Eaton Recalls Electrical Meter Breakers Due to Shock Hazard (Recall Alert)

Eaton Corporation, of Moon Township, Pa.

CPSC No agency class Dec 2, 2014

Felt Bicycles Recalls Cyclocross Bicycles Due to Risk of Injury

Felt Bicycles, of Irvine, Calif.

NHTSA No agency class Dec 1, 2014

MERCEDES-BENZ 2014: ENGINE AND ENGINE COOLING:ENGINE:DIESEL

MERCEDES-BENZ

NHTSA No agency class Dec 1, 2014

SUBARU 2003-2005: AIR BAGS

SUBARU

NHTSA No agency class Nov 28, 2014

FREIGHTLINER,WESTERN STAR 2015: SERVICE BRAKES, AIR:DISC:CHAMBER

FREIGHTLINER,WESTERN STAR

NHTSA No agency class Nov 28, 2014

INFINITI,NISSAN 2012-2015: FUEL SYSTEM, GASOLINE

INFINITI,NISSAN

FDA Food Critical Nov 26, 2014

M & M brand Number 2 Florida Avocados, packed in 50 lb cardboard boxes

M & M Farm Inc.

FDA Food Critical Nov 26, 2014

White and Wild Medley/Garden Vegetable 12/36 oz; Product number 10410. Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast Extract, Sugar. contains 2%$ of less of each of the following: dehydrated tomato, spices, natural flavor, Citric Acid, Soybean Oil, Silicon Dioxide (anticaking agent) Seasoning is added to 2 lbs of rice/grain/legume and wat

InHarvest, Inc.

FDA Food Critical Nov 26, 2014

U-TA-NE Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035

Welcome Market Inc

FDA Food Critical Nov 26, 2014

Raw Serrano Peppers packed in white cardboard box with label reading: John Vena, Inc. Serrano 5 lb Product of Mexico Packed by John Vena, Inc. Philadelphia, PA 19153 101570 or 101619

John Vena, Inc.

FDA Food Moderate Nov 26, 2014

THE ORIGINAL SOUPMAN Lobster Bisque, Net Wt 17 oz (482 g). Product is packed as a tetra pak and ships as a pack of 12 or 6 containers per carton. Distributed exclusively by: SoupMan Inc. Staten Island, NY 10314

Original Soup Man

FDA Food Critical Nov 26, 2014

Pineapple Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035

Welcome Market Inc

FDA Food Moderate Nov 26, 2014

FORMULATIONS FOR LIFE Resevera Action High Potency Longevity Complex DIETARY SUPPLEMENT, 60 VEGETARIAN CAPSULES. Distributed by: Formulations for LIfe Hauppauge, New York 11788 USA.

Formulations For Life

FDA Food Critical Nov 26, 2014

Red Bean Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035

Welcome Market Inc

FDA Food Critical Nov 26, 2014

Taro Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035

Welcome Market Inc

FDA Food Critical Nov 26, 2014

Coconut Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035

Welcome Market Inc

FDA Food Critical Nov 26, 2014

Raisin Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035

Welcome Market 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.