PlainRecalls

2013 Recalls

6,262 recalls · Page 38 of 126

2013 Recall Year Insight

Federal agencies issued 6,262 product recalls indexed by PlainRecalls in calendar year 2013. That represents about 6.16% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 17.2 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 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 2013.

On this page of 50 records, severity classification shows 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 24 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Devices Moderate Nov 6, 2013

Valiant Thoracic Stent Graft with Captivia Delivery System, Talent Thoracic Stent Graft with the Captivia Delivery System.

Medtronic Vascular, Inc.

FDA Devices Moderate Nov 6, 2013

Siemens RAPIDPoint¿¿ 405 system blood gas analyzer Product PUsage: These systems are intended for near-patient and laboratory testing of blood ga…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Nov 6, 2013

Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic imaging

Toshiba American Medical Systems Inc

FDA Devices Moderate Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, 3rd Dilator, 14 mm Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tis…

DePuy Spine, Inc.

FDA Devices Moderate Nov 6, 2013

Baxter CLEARLINK System Non-DEHP Three Lead Extension Set. 6.0" (15 cm), 1.0 mL, Luer Activated Valve, male Luer Lock Adapter, Sterile, nonpyrogenic,…

Baxter Healthcare Corp.

FDA Devices Moderate Nov 6, 2013

DRX Revolution Mobile X-Ray System, Model DRXR-1, Verona Street Rochester, NY 14608 Catalog Numbers 1019397, 1023415, 1023423 --- Made in USA by C…

Carestream Health, Inc.

FDA Devices Moderate Nov 6, 2013

HemoCue¿ Urine Albumin Microcuvettes, 25 Microcuvettes HemoCue AB Angelholm, Sweden The quantitative, rapid, turbidimetric immunoassay of albumin …

HemoCue AB

FDA Devices Critical Nov 6, 2013

Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Samp…

Atossa Genetics, Inc.

FDA Devices Moderate Nov 6, 2013

NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in the United States)

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Metasul¿ Head. Intended for use either with or without bone cement in total hip arthroplasty.

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Globus Medical MicroFuse Putty, 2.5cc and 10cc. Product Usage: MicroFuse Bone Void Filler is indicated only for bony voids or gaps that are not i…

Globus Medical, Inc.

FDA Devices Moderate Nov 6, 2013

Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Xoran MiniCAT CT Scanner

Xoran Technologies, Inc.

FDA Devices Moderate Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, Holding Clip The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissue and enabling…

DePuy Spine, Inc.

FDA Devices Moderate Nov 6, 2013

The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professiona…

GE Healthcare It

FDA Devices Moderate Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for sequential dilation of soft tissu…

DePuy Spine, Inc.

FDA Devices Moderate Nov 6, 2013

REF 5100-088, TPS Micro Driver, For Use with Stryker Total Performance System Caution Federal Law (USA) restricts the device to use by or on the …

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Nov 6, 2013

Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring Catheters. Product / Catalogue No.s: 110-4B, 110-4BC, 110-4G, 110-4H, 110…

Integra Limited

FDA Devices Moderate Nov 6, 2013

Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 MM OD. Indicated in fracture dislocation of the hip.

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Xoran MiniCAT00202

Xoran Technologies, Inc.

FDA Devices Moderate Nov 6, 2013

chromID Salmonella Agar, Reference No. 43621. A selective isolation and differentiation medium for the detection of Salmonella in human specimens.

bioMerieux, Inc.

FDA Devices Moderate Nov 6, 2013

NexGen¿ Femoral Component (CR-FLEX GSF POR FEM, C-L; CR-FLEX GSF POR FEM, C-R; CR-FLEX GSF POR FEM, C-L MINUS; CR-FLEX GSF POR FEM, C-R MINUS; CR-FLE…

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

da Vinci Si Surgical System IS3000 with the da Vinci Surgeon Console which contains a high Resolution Stereoscopic Viewer. Intended to assist in t…

Intuitive Surgical, Inc.

FDA Devices Critical Nov 6, 2013

Edwards Lifesciences EMBOL-X Glide Protection System; Model Numbers: EXGF24D, EXGF24LLD, EXGF24MMD, EXGF24SSD, EXGF24XLD, EXGF24XSD, EXGFXS2D, EXGF24…

Edwards Lifesciences, LLC

FDA Devices Moderate Nov 6, 2013

Small Bone Innovations (SBi) rHead Radial Stem, rHead Recon Radial System, rHead Radial Stem Lateral Assembly, rHead Radial Stem 6mm Collar, rHead Re…

Small Bone Innovations, Inc.

FDA Devices Moderate Nov 6, 2013

BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT), one unit per box. BrightView XCT is a gamma camera for Sing…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Nov 6, 2013

HemoCue¿ Hb 201 Microcuvettes, carton/4 boxes/25 pouches of Microcuvettes, HemoCue AB Angelholm, Sweden

HemoCue AB

FDA Devices Moderate Nov 6, 2013

Gender Solutions" Patello-Femoral Component

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

NexGen¿ Femoral Component (CR-FLEX GSF PRECOAT SZ C-L; CR-FLEX GSF PRECOAT SZ C-R ; CR-FLEX GSF PCT SZ C-L MINUS; CR-FLEX GSF PCT SZ C-R MINUS ;C…

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint 500 System: The RAPIDPoint 500 system is designed for professional us…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Nov 6, 2013

Single Site Curved Needed Driver Intuitive Surgical, Sunnyvale, CA. 94086 The Intuitive Surgical da Vinci Single-Site Instruments and Accessori…

Intuitive Surgical, Inc.

FDA Devices Moderate Nov 6, 2013

Siemens RAPIDLab¿ 1245 system blood gas analyzer Product Usage: RAPIDLab 1200 Systems: The Rapidlab 1200 systems are intended for in vitro di…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Nov 6, 2013

Vented Spike Adapter Product Code 2C0471, Sterile, nopyrogenic. Manufactured by an affiliate of Baxter Healthcare Corporation, Clintec Nutrition Divi…

Baxter Healthcare Corp.

FDA Devices Moderate Nov 6, 2013

Sidus" Head (Not distributed in the United States)

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab 1200 Systems: The Rapidlab 1200 systems are intended for in vitro diag…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Nov 6, 2013

MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG Made in Germany. Cardiopulmon…

Maquet Medical Systems USA

FDA Devices Moderate Nov 6, 2013

CPT¿ Femoral Stem (CPT 12/14 STEM SIZE 0 COCR; CPT 12/14 SIZE 0 COCR EXT; CPT 12/14 STEM SIZE 1 COCR; CPT 12/14 SIZE 1 COCR EXT CPT 12/14 STEM SIZE …

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic imaging

Toshiba American Medical Systems Inc

FDA Devices Moderate Nov 6, 2013

Single Site Bipolar Maryland Forceps Intuitive Surgical, Sunnyvale, CA. 94086 The Intuitive Surgical da Vinci Single-Site Instruments and Acces…

Intuitive Surgical, Inc.

FDA Devices Moderate Nov 6, 2013

Versys¿ Beaded Fullcoat Femoral Stem (POR FULL-CT FEM ST 11X160MM; VERSYS BEADED FC 11X200MM 8ST; POR FULLCT FEM ST 11 LOW EXT; POR FULLCT FEM ST 11 …

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic imaging

Toshiba American Medical Systems Inc

FDA Devices Moderate Nov 6, 2013

COULTER LH 750 and LH 780 Analyzers. The COULTER LH 750 Hematology Analyzer is a quantitative, automated hematology analyzer and leukocyte differ…

Beckman Coulter Inc.

FDA Devices Moderate Nov 6, 2013

Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These systems are intended for near-patient and laboratory testing of blood gase…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Nov 6, 2013

Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab 1200 Systems: The Rapidlab 1200 systems are intended for in vitro diag…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Nov 6, 2013

Natural-Knee¿ II Femoral Component

Zimmer, Inc.

FDA Devices Moderate Nov 6, 2013

Breeze C Scooter is a motorized electric scooter for elderly people. Brand name Breeze, model C. It is intended to provide increased mobility for …

S.A.E. AFIKIM

FDA Devices Moderate Nov 6, 2013

Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various i…

Ge Healthcare It

FDA Devices Moderate Nov 6, 2013

Medtronic Activa PC, model 37601, and Activa RC, model 37612, Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation. Medtronic A…

Medtronic Neuromodulation

FDA Devices Moderate Nov 6, 2013

Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile installations that combines Positron Emission Tomography (PET) and X-Ray Compute…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, 2nd Dilator, 10 mm, Insulated The PIPELINE LS Dilators and Holding Clip are intended for sequential dilation of soft ti…

DePuy Spine, Inc.

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2013 across the FDA, CPSC 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 July 2026.