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 2 critical, 43 moderate, and 5 lower-severity recalls. The page references 21 distinct recalling firms operating in 5 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (32), FDA Food (13), FDA Drug (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 Food Moderate Aug 20, 2014

Fitness Labs Fitness Multi 1, 90 capsules (UPC 654186946555) and 180 capsules (UPC 654186946609).

Nutrition Express Corporation

FDA Food Moderate Aug 20, 2014

Cool Tropics Rips Slush, Blue Raspberry Flavored 100% Juice No artificial colors or flavors, Juice from Concentrate 4 fl oz, (118 mL), Contains: Water, Apple Juice Concentrate***Manufactured in USA for Tropical Paradise, Inc., www.cool-tropics.com DO NOT MICROWAVE"

Manufacturing Solutions International

FDA Food Moderate Aug 20, 2014

Part Skim Ricotta cheese: SYSCO Imperial Ricotta Cheese packaged in 5 pound tubs and Sargento Part-Skim Ricotta Natural Cheese and Miceli's Part-Skim Ricotta Cheese packaged in 15 ounce tubs.

Miceli Dairy Products Co

FDA Food Moderate Aug 20, 2014

Lindberg B-Complex, 100mg, 60 capsules (UPC 092865239602), 240 capsules (UPC 092865239244),

Nutrition Express Corporation

FDA Food Moderate Aug 20, 2014

Ocean Garden Wild Co-treated Steak IVP 10LB 10 oz. UPC 076550080922

Blue Venture Inc.

FDA Food Moderate Aug 20, 2014

Cool Tropics Rips Slush, Sour Apple Flavored 100% Juice No artificial colors or flavors, Juice from Concentrate 4 fl oz, (118 mL), Contains: Water, Apple Juice Concentrate***Manufactured in USA for Tropical Paradise, Inc., www.cool-tropics.com DO NOT MICROWAVE" UPC Code 9 76017 00310 1

Manufacturing Solutions International

FDA Food Moderate Aug 20, 2014

Cool Tropics Rips Slush, Cherry LimeadeFlavored 100% Juice No artificial colors or flavors, Juice from Concentrate 4 fl oz, (118 mL),Manufactured in USA for Tropical Paradise, Inc., www.cool-tropics.com DO NOT MICROWAVE

Manufacturing Solutions International

FDA Food Moderate Aug 20, 2014

Sargento Light Ricotta Natural Cheese packaged in 15 ounce plastic tubs.

Miceli Dairy Products Co

FDA Food Moderate Aug 20, 2014

Uncle Ben's(R) Ready Rice GARDEN VEGETABLE, with PEAS, CARROTS, AND CORN, NET WT. 8.8 OZ (250g), UPC 5480023334

Mars Food US

FDA Food Moderate Aug 20, 2014

Sargento Whole Milk Ricotta Natural Cheese packaged in 15 ounce plastic tubs.

Miceli Dairy Products Co

FDA Food Moderate Aug 20, 2014

Lindberg B-Complex, 50mg, 60 capsules (UPC 092865236601), 120 capsules (UPC 092865236120), 240 capsules (UPC 092865236243).

Nutrition Express Corporation

FDA Food Moderate Aug 20, 2014

Farimont Foods Ricotta Cheese packaged in 30 pound bags.

Miceli Dairy Products Co

FDA Food Moderate Aug 20, 2014

Fitness Labs Fitness Multi 2, 90 capsules (UPC 654186946203) and 180 capsules (UPC 654186946227).

Nutrition Express Corporation

FDA Drug Critical Aug 20, 2014

Lite Fit USA, For Men & Women, Extreme Fat Burner, Suppresses Appetite, Boosts Metabolism, Limits Fat Absorption, Increases Energy, Prevents lipid formation by limiting fat absorption 30 pills /Bottle, Distributed by: Bacai, INC. www.litefitusa.com

Bacai Inc. Dba Ky Duyen House

FDA Drug Low Aug 20, 2014

E-Z-HD (barium sulfate) For Suspension (98% w/w), 340 g bottle, Rx Only, Manufactured by E-Z-EM Canada Inc., a subsidiary of E-Z-EM, Inc., Lake Success, NY 11042, NDC 32909-764-01.

Bracco Diagnostic Inc

FDA Drug Moderate Aug 20, 2014

Carbidopa and Levodopa Tablets USP, 25mg/100mg, 1000 count bottle, Rx only, Manufactured in Israel by Teva Pharmaceutical IND, LTD., Jeruselem, Israel, for Teva Pharmaceuticals USA, Sellersville, PA, NDC 0093-0293-10

Teva Pharmaceuticals USA

FDA Drug Low Aug 20, 2014

Depo-Medrol (methylprednisolone acetate injectable suspension USP), 40 mg/ mL, 1 mL Single-Dose Vial, Rx only, Distributed by Pharmacia & Upjohn Co Division of Pfizer Inc, New York NY 10017 NDC 0009-3073-03 DEPO-MEDROL methylprednisolone acetate Injectable Suspension USP, 40 mg per mL, 1 mL Single-Dose Vial, Rx ONLY, Distributed by Pharmacia & Upjohn Co Division of Pfizer Inc, New York NY 10017, NOVAPLUS is a registered trademark of Novation, LLC NDC 0009-3073-23

Pfizer Inc.

FDA Drug Critical Aug 20, 2014

Super ARTHGOLD 500mg, 120 Capsule Bottle, Dietary Supplement. Manufactured for & Distributed by Nanowellbeing Health, Inc., 14747 Artesia Blvd, #5V, La Mirada, CA 90638. UPC: 7 99475 35350 5.

Sung Soo Kim

FDA Devices Moderate Aug 20, 2014

Prisma M 100 PRE set. Product number 103657. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is intended as an intraoperative image-guided localization system to enable minimally invasive surgery. It links a freehand probe, tracked by a passive marker sensor system to virtual computer image space on a patient's preoperative or Intraoperative 2D or 3D image data. The system is indicated for any medical condition in which the use of stereotactic surgery may be appropriate and where a reference to a rigid anatomical structure, such as

Brainlab AG

FDA Devices Moderate Aug 20, 2014

Vl DBL OFFST WI LRG STPL, RT Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Prisma M 60 PRE set (new design). Product number 103658. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Double Offset Rasp Handle, Right Hand Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to conduct syncope examinations.

Medical Positioning Inc

FDA Devices Moderate Aug 20, 2014

Prisma TPE 2000 set. Product number 109672. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Codman Certas - In Line Valve only with SIPHONGUARD¿ Device; Product Code: 82-8804 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydrocephalus.

Codman & Shurtleff, Inc.

FDA Devices Moderate Aug 20, 2014

Prismaflex M150. Product number 109990. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

X-MARS Set (component of MARS Treatment Kit Type 1116/1 X-MARS US), Product Number 800541

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Double Offset Rasp Handle, Left Hand Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Medtronic MiniMed Guardian Monitor, Model No. CSS7100, CSS7100K Product Usage: The Medtronic MiniMed model CSS7100 and CSS7100K Guardian REAL-Time monitors are used in combination with the Minilink transmitter and Sof-sensor glucose sensor for continuous monitoring of subcutaneous glucose concentration. The information provided by these devices is intended for use in identifying potential episodes of high or low blood glucose. The information provided is not intended to be used directly for

Medtronic MiniMed Inc.

FDA Devices Low Aug 20, 2014

Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with diagnoses.

AGFA Healthcare Corp.

FDA Devices Low Aug 20, 2014

Radiomat M+ NIF 14 x 17; Radiomat SG 14 x 17 NIF; RX-B 8 x 10 in./IBF-004355; Radiomat B+ NIF 14 x 17; Radiomat B+ NIF 8 x 10; Radiomat B+ NIF 9 1/2 x 9 1/2; CX Ultra UV-G Plus NIF 11 x 14; Radiomat G Plus 14 x 17 NIF Product Usage: Radiographic film is a device that consists of a thin sheet of radiotransparent material coated on one or both sides of the film, with a radiotransparent material coated on one or both sides of the film, with a photographic emulsion intended to record images duri

AGFA Healthcare Corp.

FDA Devices Moderate Aug 20, 2014

Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydrocephalus.

Codman & Shurtleff, Inc.

FDA Devices Moderate Aug 20, 2014

Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Verigene BC-GN Test Cartridges. Each Test Cartridge comes preloaded with all required reaction solutions, including wash solutions, oligonucleotide probe solution and signal amplification solutions required to generate a test result. BC-GN is indicated for use in conjunction with other clinical and laboratory findings to aid in the diagnosis of bacterial bloodstream infections; however, is not used to monitor these infections.

Nanosphere, Inc.

FDA Devices Low Aug 20, 2014

Nanosphere Verigene Each CDF test consists of a Verigene CDF Nucleic Acid Test Kit and a Verigene CDF Amplification Reagent Kit. The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative multiplexed in vitro diagnostic test for the rapid detection of toxin A (tcdA), toxin B (tcdB), and tcdC gene sequences of toxigenic Clostridium difficile and for presumptive identification of PCR ribotype 027 strains from unformed (liquid or soft) stool specimens collected from patient

Nanosphere, Inc.

FDA Devices Moderate Aug 20, 2014

Double Offset Rasp Handle, Left Hand Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Double Offset Rasp Handle, Left Hand Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Codman Certas - In Line Valve with SIPHONGUARD¿, Unitized Catheter and Accessories; Product Code: 82-8806 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydrocephalus.

Codman & Shurtleff, Inc.

FDA Devices Moderate Aug 20, 2014

23.5 Deg Rasp Handle Assy- RIGHT Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Prismaflex HF 1000. Product number 107140. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Prisma HF1000 preset (new design). Product number 107639. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs, Lot 1320 VITROS¿ CA 19-9 Reagent Packs are used on VITROS¿ ECi/ECiQ Immunodiagnostic Systems, VITROS¿ 3600 Immunodiagnostic Systems and VITROS¿ 5600 Integrated Systems for the quantitative measurement of 1116-NS-19-9 defined antigen in human serum and plasma.

ORTHO-CLINICAL DIAGNOSTICS

FDA Devices Moderate Aug 20, 2014

DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull, spinal column and extremities, check abdomen and other both parts.

AGFA Healthcare Corp.

FDA Devices Moderate Aug 20, 2014

IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace Portal (ISP) is a multimodality (CT, NM, and MR) thin-client applications server that delivers full diagnostic viewing and clinical applications to the enterprise. IntelliSpace Portal (ISP) is a medical software system that allows multiple users to remotely access IntelliSpace Workspace Portal (ISP) from compatible computers on a network. The system allows networking, selectio

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Aug 20, 2014

VI DBL OFFST W/ LRG STPL, LT Nonsterile

Zimmer, Inc.

FDA Devices Moderate Aug 20, 2014

Prismaflex M100. Product number 106697. Each set is packaged in a plastic pouch, 4 pouches per carton box

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Codman Certas - In Line Valve with SIPHONGUARD¿ Device, Unitized BACTISEAL¿ Catheter and Accessories; Product Code: 82-8807 The Codman Certas Programmable valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of hydrocephalus.

Codman & Shurtleff, Inc.

FDA Devices Moderate Aug 20, 2014

PrisMARS Kit (component of MARS Treatment Kit Type 1115/1 PrisMARS US), 1 MARS Treatment Kit per carton box, Product Number 800480, Batch

Gambro Renal Products, Incorporated

FDA Devices Moderate Aug 20, 2014

Integra NewPort MIS System Model No. NWPIMP (NewPort Implant Tray w/ Components) NWP2INSTP (NewPort Instrument Tray w/ Components) The NewPort System is intended to be used as a temporary or permanent posterior, non-cervical implant to correct spinal disorders and provide stabilization of the spine to permit the biological process of spinal fusions to occur.

Integra LifeSciences Corp.

FDA Devices Moderate Aug 20, 2014

Double Offset Rasp Handle, Left Hand Nonsterile

Zimmer, 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.