PlainRecalls

2014 Recalls

6,290 recalls · Page 62 of 126

2014 Recall Year Insight

Federal agencies issued 6,290 product recalls indexed by PlainRecalls in calendar year 2014. That represents about 7.49% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.2 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 126 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, 48 moderate, and 0 lower-severity recalls. The page references 26 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (46), FDA Drug (4), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Jul 9, 2014

HCG (Human Chorionic Gonadotropin) + Methylcobalamin (Methyl B12), 1500 units + 1000 mcg/mL drop, 8 mL bottle, Rx only, MD Custom Rx, 19035 W. Capit…

Brookfield Prescription Center Inc. dba MD Custom Rx

FDA Drug Moderate Jul 9, 2014

Brevibloc Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2,500 mg/250 mL (10 mg/mL), 250 mL Single Use IntraVia container, packaged in…

Baxter Healthcare Corp.

FDA Drug Moderate Jul 9, 2014

Bystolic (nebivolol) tablets, 20 mg/tablet. 7 Tablet Professional Sample Bottle, Rx Only. Forest Pharmaceuticals, Inc., Subsidiary of Forest Laborat…

Forest Pharmaceuticals Inc

FDA Drug Moderate Jul 9, 2014

HCG (Human Chorionic Gonadotropin) 200 units/ 0.1 mL drops, packaged in 5 mL and 10 mL bottles, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105…

Brookfield Prescription Center Inc. dba MD Custom Rx

FDA Devices Critical Jul 9, 2014

Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Catalog No. 46914. Intended to allow drainage and measurement o…

Medtronic Neurosurgery

FDA Devices Moderate Jul 9, 2014

Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE Product Usage: The Triathlon Tritanium Patella Inserter is part of the T…

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Jul 9, 2014

GE Healthcare, Revolution XR/d. Revolution XR/d Intended Use: The Revolution XR/d Digital Radiographic imaging system is indicated for use in gen…

GE Healthcare, LLC

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 1. Part of the NexGen systems of …

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 3. Part of the NexGen systems of …

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 5. Part of the NexGen systems of …

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

GE Healthcare, Proteus XR/a. Proteus XR/a Intended Use: Is intended for use in generating radiographic images of human anatomy in all general purp…

GE Healthcare, LLC

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…

Claymount Assembli

FDA Devices Moderate Jul 9, 2014

IRK QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System and Si-e. Intuitive Surgical Endoscopic Instrument C…

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.

Blue Belt Technologies MN

FDA Devices Moderate Jul 9, 2014

Suture Set, 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

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 7. Part of the NexGen systems of …

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

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

Medical Action Industries Inc

FDA Devices Moderate Jul 9, 2014

Integra¿ LED Battery Charger, Single Bay. Product Number: 90523 The LED Headlight System Battery Charger (90523) is an accessory to the LED Hea…

Integra LifeSciences Corp.

FDA Devices Moderate Jul 9, 2014

Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part Number 585006 contained in Alcon Assembly Numbers 9795-37, 11233-14, and 1333…

Alcon Research, Ltd.

FDA Devices Moderate Jul 9, 2014

NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 2. Part of the NexGen systems of …

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

System Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument Contro…

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Max Barrier Kit, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

Medical Action Industries Inc

FDA Devices Critical Jul 9, 2014

Langston Dual Lumen Catheters, 6Fr, REF 5550 and 5540. The Vascular Solutions Langston Dual Lumen Pressure Monitoring catheter is used as a pressure …

Vascular Solutions, Inc.

FDA Devices Moderate Jul 9, 2014

MIS Rod 2, a component of the NewPort System. Model No: 60-0545 (45mm); 60-0550 (50mm); 60-0555 (55mm); 60-0560 (60mm); 60-0575 (75mm); 60-0580 (8…

Integra LifeSciences Corp.

FDA Devices Moderate Jul 9, 2014

MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus instrument access door hinge. Siemens Healthcare Diagnostics, Inc. in vitro …

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jul 9, 2014

Connection QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic Instrument Co…

Intuitive Surgical, 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…

Zimmer, Inc.

FDA Devices Moderate Jul 9, 2014

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

Medical Action Industries Inc

FDA Devices Moderate Jul 9, 2014

CNS-6200 Series Central Nurse Station and accessories. Model Number: CNS-6201 For cardiac and vital signs monitoring for multiple patients.

Nihon Kohden America Inc

FDA Devices Moderate Jul 9, 2014

Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips (Reusable) Ref 3222

Microline Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

Stapler Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instrument C…

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 9, 2014

ADVIA Centaur¿ Systems TnI-Ultra assay; Catalog Number 02789602 (100 tests), SMN 10317708 and 02790309 (500 tests), SMN 10317790

Siemens Healthcare Diagnostics, Inc

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 Con…

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 …

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. …

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 …

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 Contr…

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 …

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 …

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. …

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…

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…

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 …

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 us…

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 Ins…

Intuitive Surgical, 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: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2014