PlainRecalls

2013 Recalls

6,215 recalls · Page 99 of 125

2013 Recall Year Insight

Federal agencies issued 6,215 product recalls indexed by PlainRecalls in calendar year 2013. That represents about 7.40% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.0 recalls per day across the FDA, CPSC, 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 125 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 2013.

On this page of 50 records, severity classification shows 4 critical, 44 moderate, and 2 lower-severity recalls. The page references 33 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 (42), FDA Drug (8), 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 2013 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 100 mcg, packaged in a) 100-count bottles (NDC 60793-854-01) and b) 1000-count bottles ( NDC 60793-854-10…

Pfizer Inc.

FDA Drug Moderate Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 50 mcg, packaged in a) 100-count bottles (NDC 60793-851-01) and b) 1000-count bottles ( NDC 60793-851-10 …

Pfizer Inc.

FDA Drug Moderate Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 112 mcg, packaged in a) 100-count bottles (NDC 60793-855-01) and b) 1000-count bottles ( NDC 60793-855-10…

Pfizer Inc.

FDA Drug Moderate Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 137 mcg, packaged in a) 100-count bottles (NDC 60793-857-01) and b) 1000-count bottles ( NDC 60793-857-10…

Pfizer Inc.

FDA Drug Moderate Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 175 mcg, packaged in a) 100-count bottles (NDC 60793-859-01) and b) 1000-count bottles ( NDC 60793-859-10…

Pfizer Inc.

FDA Drug Moderate Apr 24, 2013

Levoxyl (levothyroxine sodium) tablets, USP 200 mcg, packaged in a) 100-count bottles (NDC 60793-860-01) and b) 1000-count bottles ( NDC 60793-860-10…

Pfizer Inc.

FDA Drug Low Apr 24, 2013

buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg, 30-count tablets per bottle, Rx only, Distributed by: Actavis South Atlantic LLC, Sunri…

Actavis South Atlantic LLC

FDA Drug Critical Apr 24, 2013

Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.

Hospira Inc.

FDA Devices Moderate Apr 24, 2013

EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and Accessories Part number C02033-01. Label reads in part "EsophyX2 2-LINK Device Q…

Endogastric Solutions Inc

FDA Devices Moderate Apr 24, 2013

VITROS 4600 Chemistry System (VITROS 5,1 FS System family member), Product Code 6802445. Intended for use in the measurement of a variety of chemi…

Ortho-Clinical Diagnostics

FDA Devices Moderate Apr 24, 2013

REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422763 Oxford Mlcroplasty Knee System Tibial instrument Tray …

Biomet U.K., Ltd.

FDA Devices Moderate Apr 24, 2013

Clinical Chemistry Phenobarbital, list number 1E08

Abbott Laboratories, Inc

FDA Devices Moderate Apr 24, 2013

GE Healthcare, AW Server. Product Usage: . AW Server is a medical software system that allows multiple users to remotely access AW applications f…

GE Healthcare, LLC

FDA Devices Moderate Apr 24, 2013

The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product U…

Synvasive Technology Inc

FDA Devices Moderate Apr 24, 2013

LifeScan brand OneTouch¿ Select Control Solution, Part Number/Model #: 02168902. Testing of Blood Glucose Levels.

Lifescan Inc

FDA Devices Low Apr 24, 2013

IMO-402 Mononucleosis Rapid Test Device (Whole Blood/Serum/Plasma). Catalog #IMO-402/94201 The MONO test (Whole Blood) is a rapid chromatographic…

Alere San Diego, Inc.

FDA Devices Moderate Apr 24, 2013

VITROS 5600 Integrated System, Product Code 6802413. Intended for use in the measurement of a variety of chemistry analytes.

Ortho-Clinical Diagnostics

FDA Devices Moderate Apr 24, 2013

EVOTECH Endoscope Cleaner and Reprocessor System, P/N 50004. Designed to automatically clean and high-level disinfect flexible, submersible video …

Advanced Sterilization Products

FDA Devices Moderate Apr 24, 2013

The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic inf…

Hospira Inc.

FDA Devices Moderate Apr 24, 2013

SR Instruments FG3105 Patient Scales Used on various Joerns Healthcare Patient Lifters. Model# FG3105 Patient Scales. Product Usage: The FG310…

Sr Instruments Inc

FDA Devices Moderate Apr 24, 2013

Vitrea CT Multi-Chamber Cardiac Functional Analysis application on Vitrea version 5.2 (Vitrea Enterprise Suite 1.3 and Vitrea fX 3.1) and subsequent …

Vital Images, Inc.

FDA Devices Moderate Apr 24, 2013

TRIGEN (TM) L-P SCREW, 4.5 MM X 37.5 MM, TI-6AL-4V, QTY: (1), STERILE R, REF 71645437, Smith & Nephew, Inc. Memphis, TN 38116 USA orthopedic surge…

Smith & Nephew Inc

FDA Devices Moderate Apr 24, 2013

Edwards Lifesciences Crimpers, Model 9100CR26. The Crimpers are used to crimp the transcatheter heart valve onto the delivery system prior to us…

Edwards Lifesciences, LLC

FDA Devices Moderate Apr 24, 2013

HCS3011 AV Loop Kit For use with Transonic CO status System Only, -HCS3021 AV Loop Kit For use with Transonic CO status System Only. Product Usa…

Transonic Systems Inc

FDA Devices Critical Apr 24, 2013

ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are intended to be used as patient-specific surgical instrumentation to as…

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Apr 24, 2013

Accuray CyberKnife System Medical Physicist, Robotic Radiosurgery System, Medical charged-particle radiation therapy system, Model: Iris Variable Ape…

Accuray Incorporated

FDA Devices Moderate Apr 24, 2013

MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version 3.3.0.0) Product Usage: The Cardiohelp System is a blood oxygenation and …

Maquet Cardiovascular, LLC

FDA Devices Moderate Apr 24, 2013

CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used with the CoagCHEK XS Pro Meters to quantitatively determines prothrombi…

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Apr 24, 2013

ADVIA Centaur Vitamin D Assay (100 tests); Reference Number: 10491994. For use in the quantitative determination of Vit D.

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Apr 24, 2013

Duane Reade TRUEtrack monitor kit, UPC# 6 39194 01679 7 Part # A4006-81 The TRUEtrack Blood Glucose System is intended for the quantitative determ…

Nipro Diagnostics, Inc.

FDA Devices Moderate Apr 24, 2013

OsteoSelect DBM Putty Product Usage: Orthopedic bone filler

Bacterin International, Inc.

FDA Devices Moderate Apr 24, 2013

IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical System and da Vinci Si-e Surgical System, Model SI3000. Arm drapes protect equipmen…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 24, 2013

IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System, Model IS2000. Arm drapes protect equipment from contamination.

Intuitive Surgical, Inc.

FDA Devices Critical Apr 24, 2013

All OneTouch Verio IQ Blood Glucose Meters sold as: Verio IQ System Kits - Meter; Verio IQ Starter kits - Meter; Verio IQ Warranty Meter. Pro…

Lifescan Inc

FDA Devices Moderate Apr 24, 2013

ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner. Used with the ACCU-CHEK Inform II System to quantitatively measure glucose …

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Apr 24, 2013

DeGotzen XRay unit XGenus Dental X-ray unit.

DeGotzen

FDA Devices Moderate Apr 24, 2013

Alere Cholestech LDX ALT AST Test Cassette, Model #12-788. For the in vitro quantitative determination of alanine aminotransferase (ALT) and aspar…

Alere San Diego, Inc.

FDA Devices Moderate Apr 24, 2013

Aplio 500/400/300 Diagnostic Ultrasound System (TUS-500/400/300). Device Listing Number: Dl53118. Diagnostic Ultrasound system.

Toshiba American Medical Systems Inc

FDA Devices Moderate Apr 24, 2013

HORIBA ABX PENTRA 400 I.S.E. Module, Model Numbers: P400ISE110EN02 and P400ISE110US02, All Serial Numbers, Software Versions 5.0.7 and Below. Used…

Horiba Instruments, Inc dba Horiba Medical

FDA Devices Moderate Apr 24, 2013

Elana Catheter Sizer 2.0*** The Elana Catheter Sizer 2.0 is designed to aid the surgeon to assess the bypass graft of the ELANA technique.

Elana, Inc.

FDA Devices Critical Apr 24, 2013

Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply co…

Carefusion Corporation

FDA Devices Moderate Apr 24, 2013

Edwards Lifesciences Crimpers, Model 9100CR23. The Crimpers are used to crimp the transcatheter heart valve onto the delivery system prior to us…

Edwards Lifesciences, LLC

FDA Devices Moderate Apr 24, 2013

Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R) Workflow SLR is a digital …

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Apr 24, 2013

ACIST Medical Systems Inc. The ACIST Angiographic Injection System is intended to be used for the controlled infusion of radiopaque contrast media…

Acist Medical Systems

FDA Devices Moderate Apr 24, 2013

Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply …

Carefusion Corporation

FDA Devices Moderate Apr 24, 2013

GE Healthcare, Innova 2100IQ, Innova 3100IQ, Innova 4100IQ, Cardiovascular and Interventional Imaging System.

GE Healthcare, LLC

FDA Devices Moderate Apr 24, 2013

Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Apr 24, 2013

VITROS 5,1 FS Chemistry System, Product Code 6801375 and VITROS 5,1 FS Chemistry System Refurbished, Product Code 6801890. Intended for use in the…

Ortho-Clinical Diagnostics

FDA Devices Moderate Apr 24, 2013

Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc. (El Dorado Hills, CA) & manufactured under Synvasive Technology, Inc. E…

Synvasive Technology Inc

FDA Devices Moderate Apr 24, 2013

Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The cannulae are intended for use in situations which require rapid femor…

Edwards Lifesciences, LLC

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2013 with 2012 →

Data Sources

  • Source: FDA openFDA Enforcement API — calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA — consumer product and vehicle recall feeds for 2013