PlainRecalls

2014 Recalls

7,499 recalls · Page 108 of 150

2014 Recall Year Insight

Federal agencies issued 7,499 product recalls indexed by PlainRecalls in calendar year 2014. That represents about 8.93% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.5 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 150 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 1 critical, 48 moderate, and 1 lower-severity recalls. The page references 23 distinct recalling firms operating in 4 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (45), CPSC (4), NHTSA (1), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Mar 19, 2014

Gyrus ACMI Disposable Falope-Ring Band Applicator Kits. REF 006889-901 and REF 005280-901 (with 8 mm Disposable Trocan). Sterile EO. Single Use On…

Gyrus Medical, Inc

FDA Devices Moderate Mar 19, 2014

VERIFY¿ SixCess 270FP Challenge Pack, STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060, 440-354-2600. The VERIFY¿ SixCess 270FP Challenge P…

Steris Corporation

FDA Devices Moderate Mar 19, 2014

Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data. T…

Mindray DS USA, Inc. dba Mindray North America

FDA Devices Moderate Mar 19, 2014

GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging p…

GE Healthcare, LLC

FDA Devices Moderate Mar 19, 2014

G1777: Umbilical (2) 3 mL Line Draw, Luer lock syringes (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ devices and (2) Needle-Pro¿ Devic…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with Q-CPR Meter Option B08 The HeartStart MRx is for use for the terminat…

Philips Medical Systems, Inc.

FDA Devices Moderate Mar 19, 2014

RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588. General ophthalmic imaging in…

Clarity Medical Systems Inc

FDA Devices Moderate Mar 19, 2014

Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave processing.

Biomet 3i, LLC

FDA Devices Moderate Mar 19, 2014

G2001: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device, Needle-Pro¿ Device and 23G x 1 needle …

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

4043G-2: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device and ice bag Arterial Blood Sampling …

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wound therapy pu…

Smith & Nephew Inc.

FDA Devices Moderate Mar 19, 2014

4043E: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device (for sale in Europe only) Arterial Bloo…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

VerifyNow IIb/IIIa Test, Catalog No. 85310, 10-Test Kit and Catalog No. 85011, 25-Test kit. Product Usage: The VerifyNow System is a turbidimetr…

Accumetrics Inc

FDA Devices Moderate Mar 19, 2014

Hand Control 12FR Suction Coagulator with 10 ft cord and holster, Sterile, Disposable, Model Number 0043-25, packaged Tyvek¿ polyester peel pouch, 25…

Megadyne Medical Products, Inc.

FDA Devices Moderate Mar 19, 2014

4042E: 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device (for sale in Europe only) Arterial Blo…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794, 66800795, and 66800796 (The RENASYS Soft Port Dressing Kits are used i…

Smith & Nephew Inc.

FDA Devices Moderate Mar 19, 2014

G1762: 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device, syringe tip cap, and 5 mL Luer lock syrin…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

REF 623401 R, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right, Medium, Sterile R Qty 1 The S-ROM Hinged knee femo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Mar 19, 2014

REF 623411 L, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Left, Small, Sterile R Qty 1 The S-ROM Hinged knee femora…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Mar 19, 2014

HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis IHC PR Breast Tissue Manual Read of Digital Slides The ScanScope¿¿ …

Leica Biosystems Imaging, Inc.

FDA Devices Moderate Mar 19, 2014

CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II¿ is a semi-automated fluorescence microscope, consisting …

Veridex, LLC

FDA Devices Moderate Mar 19, 2014

REF 623401 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Left, medium, Sterile R Qty 1 The S-ROM Hinged knee femor…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Mar 19, 2014

G1725: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device and 1 mL Line Draw Luer slip syringe (hepa…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

REF 623421 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Left , X-Small, Sterile R Qty 1 The S-ROM Hinged knee femo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Mar 19, 2014

Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A, M3536A, M3536M,M3536M4,M3536M6,861288,861289,861464,861483,and 861491

Philips Medical Systems, Inc.

FDA Devices Moderate Mar 19, 2014

Smith & Nephew RENASYS-G Sterile, Gauze Dressing Kit with Soft Port REF #'s: 66800961 (The RENASYS Soft Port Dressing Kits are used in conjunction …

Smith & Nephew Inc.

FDA Devices Moderate Mar 19, 2014

Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933, 66800934, 66800935, and 66800936 (The RENASYS Soft Port Dressing Kits are used …

Smith & Nephew Inc.

FDA Devices Moderate Mar 19, 2014

Cannabinoids DAU Calibrator Control Level 1 (37.5 ng/mL) This solution is prepared from non-sterile urine and should be handled as potentially inf…

Lin-Zhi International Inc

FDA Devices Low Mar 19, 2014

VITROS Immunodiagnostic Products 25-OH Vitamin D Total Calibrators; REF/CATALOG # 684 4055, IVD --- COMMON/USUAL NAME: VITROS Vitamin D Calibrators -…

Ortho-Clinical Diagnostics

FDA Devices Moderate Mar 19, 2014

Navigator Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave processing.

Biomet 3i, LLC

FDA Devices Moderate Mar 19, 2014

bioMerieux PREVI Isola System (General purpose,microbiology, diagnostic Medical Device), (REF 29500/29500R), bioMerieux, Hazelwood, MO.

Biomerieux Inc

FDA Devices Moderate Mar 19, 2014

G1469J: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device (for sale in Japan only) Arterial Blo…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239 CARESCAPE Monitor B650 The CARESCAPE Monitor B650 is a multi-parameter pa…

GE Healthcare, LLC

FDA Devices Moderate Mar 19, 2014

Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave processing.

Biomet 3i, LLC

FDA Devices Moderate Mar 19, 2014

MAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat Exchanger is used as part of a cardioplegia system to set and maintain te…

Maquet Cardiovascular Us Sales, Llc

FDA Devices Moderate Mar 19, 2014

GE Healthcare Infinia and Infinia Hawkeye Nuclear Medicine Systems. For Dual-Head Variable Angle Gamma Camera, Hawkeye Option for Dual-Head Variab…

GE Healthcare, LLC

FDA Devices Moderate Mar 19, 2014

Smith & Nephew RENASYS-F XL with Soft Port REF #: 66800797 (The RENASYS Soft Port Dressing Kits are used in conjunction with negative pressure wou…

Smith & Nephew Inc.

FDA Devices Moderate Mar 19, 2014

REF 623421 RS-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right , X-Small, Sterile R Qty 1 The S-ROM Hinged knee femo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Mar 19, 2014

XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam radiation therapy or brachythera…

Elekta, Inc.

FDA Devices Moderate Mar 19, 2014

Contra-Angle Torque Driver Kit For Certain Internal Connection Product Usage: Molded plastic tray used in holding various dental instruments for …

Biomet 3i, LLC

FDA Devices Moderate Mar 19, 2014

4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device, 22g x 1¿ needle, and Point-Lok…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

Mar Cor Purification CWP Reverse Osmosis System. Models 101, 102, 104, and 106.

Mar Cor Purification

FDA Devices Moderate Mar 19, 2014

Contra-Angle Torque Driver Kit For Certain and External Connection Product Usage: Molded plastic tray used in holding various dental instruments …

Biomet 3i, LLC

FDA Devices Moderate Mar 19, 2014

4043W-2: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device, syringe tip cap and 6 mL Luer slip syri…

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 19, 2014

4043-2: 3 mL Line Draw, Luer slip syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device Arterial Blood Sampling Line Draw Syr…

Smiths Medical ASD, Inc.

CPSC Moderate Mar 19, 2014

Ganz Recalls Grumpy Cat Stuffed Animal Toys Due to Choking Hazard

Ganz USA LLC, Marietta, Ga.

CPSC Moderate Mar 19, 2014

Vera Bradley Recalls Bear Ring Rattles and Bunny Toys Due to Choking Hazard

Vera Bradley Designs Inc., of Fort Wayne, Ind.

NHTSA Critical Mar 19, 2014

INFINITI 2014: EQUIPMENT:OTHER:LABELS

INFINITI

CPSC Moderate Mar 18, 2014

Arctic Cat Recalls Off-Highway Utility Vehicles Due to Fuel Leak and Fire Hazard (Recall Alert)

CPSC Moderate Mar 18, 2014

Schneider Electric Recalls Square D-Brand F and K Frame Circuit Breakers Due to Fire Hazard

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 — consumer product and vehicle recall feeds for 2014