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 10 critical, 39 moderate, and 1 lower-severity recalls. The page references 27 distinct recalling firms operating in 3 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (36), FDA Food (9), 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 Critical Jul 2, 2014

William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer, 8 oz. (227g) package; Dietary Fiber, Raw, Sprouted.

Navitas, LLC., dba Navitas Naturals

FDA Food Critical Jul 2, 2014

Oceans Cuisine brand CRAB STUFFING WITH REAL CRABMEAT, NET WEIGHT 3 LBS. (48 oz.) UPC 7 30692 00031 5, PRODUCT OF USA --- PACKED BY: OCEANS CUISINE LTD. FARMINGDALE, NY 11735 --- The product is packaged in plastic tub containers, 2 x 3 lb. containers per case

Oceans Cuisine, LTD.

FDA Food Critical Jul 2, 2014

Gouda Cheese wheels, Whole Wheels 10 lbs and Half Wheels 5 lbs., packaged under the the brand names: Mountain Gouda and Smiths Farmstand

Smith's Country Cheese, Inc.

FDA Food Low Jul 2, 2014

Marissa Collection Tangerine Appetizer Plate Set (set of 2). distributed by Princess House Inc., Taunton, MA

Princess House Inc.

FDA Food Critical Jul 2, 2014

Dark Old Fashioned Sponge Candy, sold under the following brand and sizes: 1. Eillien's in Net Wt. 6 oz (170g) UPC 34952-12994, 10 oz. (284g) UPC 34952-56927, 12 oz. (340g) UPC 34952-57307. 2. Blain's Farm & Fleet Net Wt. 14oz. (397g), UPC 34952-81171 3. Mae's Corner Market Net Wt. 14oz. (397g) UPC 34952-41075, 1 lb. 8 oz. (680g) UPC 34952-41098, and Premium Party Tray, Net Wt. 58.5 oz.(1687g) UPC 34952-41324. 5. Mrs. Kimball's Candy Shoppe, Net Wt 13 oz(369g) PCA3-13956. 6. Piggly

Eillien's Candies, Inc.

FDA Food Critical Jul 2, 2014

Navitas Naturals Omega Blend Sprouted Smoothie Mix, 8 oz. (227g) package; Dietary Fiber, Raw, Sprouted. UPC 858847000314; Also packaged for Williams Sonoma Omega Smoothie Mixer; SKU 506436 Navitas Naturals, Novato, CA

Navitas, LLC., dba Navitas Naturals

FDA Food Critical Jul 2, 2014

GreenSmoothieGirl TriOmega Superfood, GreenSmoothieGirl Sprouted Ground TriIOmega Superfood, Packaged in metalized resealable standup pouches in 1-pound units

Green Smoothie Girl

FDA Food Critical Jul 2, 2014

GSF LLC Shelled Walnuts, Kernel Combo Halves & Pieces, 15% New Wt. 25 lbs. GSF LLC, Visalia, CA 93290

GSF Nut Company LLC

FDA Food Critical Jul 2, 2014

Floribbean Key Lime Calypso Dip 12.5 oz Floribbean 68 SW 40 St. Suite 411 Miami, Florida 33155 1(800)282-8459

Miami Interculinary Center, Inc.

FDA Drug Moderate Jul 2, 2014

Gemcitabine For Injection USP, 1 g, (lyophilized), For Intravenous Use Only, Sterile Single Use Vial, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd, Gujarat, India, NDC 47335-154-40

Caraco Pharmaceutical Laboratories, Ltd.

FDA Drug Moderate Jul 2, 2014

Sodium Chloride Hypertonicity Ophthalmic Ointment, 5%, 1/8 oz. (3.5 g) tube per carton, Distributed by Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-5315-38, UPC 3 09045 31538 5.

Bausch & Lomb, Inc.

FDA Drug Moderate Jul 2, 2014

Dextroamphetamine Sulfate Tablets, USP, 10 mg, 100-count bottles, Rx only, Barr Laboratories, Inc., Pomona, NY 10970, NDC 0555-0953-02.

Teva Pharmaceuticals USA

FDA Drug Moderate Jul 2, 2014

Pristiq (desvenlafaxine) Extended-Release Tablets 50 mg, 30 count bottle, Rx only, Distributed by Wyeth Pharmaceuticals, Inc., NDC 0008-1211-30

Pfizer Us Pharmaceutical Group

FDA Drug Moderate Jul 2, 2014

Muro 128 (sodium chloride) hypertonicity ophthalmic ointment, 5%, packaged in a) 1 g tube per carton, professional sample, NDC 24208-385-01, UPC 3 24208-385-01 2; b) 1/8 oz. (3.5 g) tube per carton, NDC 24208-385-55, UPC 3 24208-385-55 5; and c) 1/4 oz. (7 g) Twin Pack, Two 1/8 oz. (3.5 g) tubes per carton, NDC 24208-385-56, UPC 3 24208-385-56 3; Bausch & Lomb Incorporated, Tampa, FL 33637.

Bausch & Lomb, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0033***Custom Autolube Food Guard***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-302 Lactate , 40, Potassium 1, Sodium 140, Calcium 3, Magnesium 1, Chloride 105, Glucose (mg/dL) 100, Batch Size (liters): 60 The SAK is one of the disposables used with NxStage PureFlow SL Dialysate Preparation System. The SAK is a disposable bag pre-filled with dialysate concentrate that is then filled with purified water prepared by NxStage PureFlow SL Dialysate Preparation System to prepare a batch of d

NxStage Medical, Inc.

FDA Devices Moderate Jul 2, 2014

UniCel DxH 800 Coulter Cellular Analysis System, Part No. 629029, B24465, and B24802. Used for in vitro diagnostic use in screening patient populations found in clinical laboratories.

Beckman Coulter Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***MA Attachment, Straight version Custom***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

UniCel DxH 600 Coulter Cellular Analysis System, Part No. B23858. Used for in vitro diagnostic use in screening patient populations found in clinical laboratories.

Beckman Coulter Inc.

FDA Devices Moderate Jul 2, 2014

NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow SL REF: SAK-305 Lactate 45, Potassium 1, Sodium 140, Calcium 3, Magnesium 1 Chloride 100, Glucose (mg/dL) 100 Batch Size (liters) 40

NxStage Medical, Inc.

FDA Devices Moderate Jul 2, 2014

IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed for use in physical therapy, rehabilitation, and pain relief applications.

Zynex Medical, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***Custom QD11 Attachment with thinner nose tube***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Critical Jul 2, 2014

HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Standard Shaft, Straight Tip, 150 CM Length Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures.

Nitinol Devices and Components, Inc.

FDA Devices Moderate Jul 2, 2014

Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)

Western / Scott Fetzer Company

FDA Devices Moderate Jul 2, 2014

Shaver Handpiece Sterilization Tray. Model number 272-700-000. For sterilization of Stryker Endoscopy arthroscopic shaver.

Stryker Endoscopy

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0023***Custom 5 cm Extension Bearing Sleeve***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or non-invasive ventilatory support and monitoring for infant, pediatric, and adult patients with respiratory failure or respiratory insufficiency. It is used in hospitals and healthcare facilities.

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA Devices Moderate Jul 2, 2014

ANSPACH***Modified QD11 Attachment with Soft Tissue Protector***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4604-00***3mm Fluted Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

Accell Evo3C Demineralized Bone Matrix, 5 cc, Model Number: 02-6000-050 , Lot Number: 132160. Product Usage: Accell Evo3c Demineralized Bone Matrix Putty is intended for filling voids and gaps in the skeletal system that are not intrinsic to the stability of the bony structure. Accell Evo3c is indicated for use as a bone graft extender in the spine, extremities and pelvis, or as a bone void filler in the extremities and pelvis. The voids or gaps may be surgically created defects or

Integra LifeSciences Corp.

FDA Devices Moderate Jul 2, 2014

Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum.

JAS Diagnostics Inc.

FDA Devices Moderate Jul 2, 2014

Coulter DxH Cleaner 5L, Part No. 628022. For use on UniCel DxH Systems for components that come in contact with blood samples.

Beckman Coulter Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-3012-00***13 mm Drill with Depth Stop for Short Heavy Duty Attachment***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0022***8 mm Coarse Headless Screw with Driver***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0042***XMax Motor with Custom Hose***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-5000-00***Threaders, Arthroscopic Suture Anchor***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

Siemens StreamLAB(R) Analytical Workcell; Catalog number 746002.901. Designed to automate sample handling and processing in the clinical laboratory.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0035***Custom eMax 2 Plus Motor with microMax Disconnect Sleeve***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Critical Jul 2, 2014

HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures.

Nitinol Devices and Components, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4601-00***1mm Coarse Diamond Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

Integra UCR 3mm Hex, Large Axial Driver. The UCR Hex Axial Driver is a surgical instrument used to implant and remove polyaxial screws of varying reduction heights provided with the Malibu", UCR, and NewPort" Systems. The Malibu", UCR, NewPort" Systems are 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. Accepted standard techniques of

SeaSpine Inc

FDA Devices Moderate Jul 2, 2014

Ingenia 3.0T, magnetic resonance imaging system.

Philips Medical Systems, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4605-00***Arthroscopic Suture Anchor assembly with Suture Threader***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0020***Modified Arthroscopic Knotless Suture Anchor Deployment Tool with Suture Puller***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***Arthroscopic Knotless Suture Anchor***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0048***Custom Circular ePLUS-FP***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, Inc.

FDA Devices Moderate Jul 2, 2014

Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing ADVIA Centaur Acid Reagent bottles, lot number: 454778 Kit Catalog Number: 112219 SMN: 10310026 Intended Use: In vitro diagnostic use. Acid Regent is a component of the ADVIA Centaur and ADVIA Centaur XP instruments

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Jul 2, 2014

SteriGear Urinary Drain Bag with Fig Leaf Cover, 2000 ml, REF 10270, The Fig Leaf, SteriGear 362 S. University Avenue, provo, UT 84601, 1-800-398-3259, SteriGear.com, Sterile, EO Urinary Drainage Collection Kit, for Indwelling Catheter. This device is intended to collect the Urine drained from an indwelling catheter

SteriGear, LLC

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0019***Modified MDA Tube with MA-D20 Attachment***Rx Only*** This device is intended to be used with Anspach Systems

The Anspach Effort, 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.