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 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 11 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 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 Devices Moderate Apr 16, 2014

Dengue IgG/IgM; LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Buprenorphine Test Strip; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Morphine Strip (300); LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

10mm Drain Kit Flat 3/4 Perforated with 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage

Aspen Surgical Products, Inc.

FDA Devices Moderate Apr 16, 2014

FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down. Electrical extension cable intended to transmit signal from, or power or excitation signal to patient connected electrodes. The cable is a sterile, disposable device.

Remington Medical Inc.

FDA Devices Moderate Apr 16, 2014

Fentanyl Test Card; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

7mm Drain Kit Flat Full Perforated with Trocar and 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage

Aspen Surgical Products, Inc.

FDA Devices Moderate Apr 16, 2014

Tuberculosis Antibody Test Card Serum; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Ketamine Test Card; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Clonazepam Test Card; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Saber 100ml Infection Control PVC Bulb Evacuator, Sterile (10/case) Intended to provide manual suction and collection of fluids for closed wound drainage systems

Aspen Surgical Products, Inc.

FDA Devices Moderate Apr 16, 2014

PSA Test Card (Whole Blood); LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

CK-MB Test Card (serum); LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Troponin I test Card (serum); LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

15FR Drain Kit Round End Perforated with Trocar and 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drainage

Aspen Surgical Products, Inc.

FDA Devices Moderate Apr 16, 2014

K2 (synthetic Marijuana) Test Strip; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Cobas c8000 Modular Analyzer Series Cobas c502, Part Number 5964067001, a clinical chemistry analyzer intended for the in vitro quantitative / qualitative determination of analytes in body fluids.

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Apr 16, 2014

Tramadol Test Card; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.

Energizer Personal Care

FDA Devices Moderate Apr 16, 2014

Rotavirus Test Card LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

H. Pylori Antibody Test Card (Whole Blood) LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity conditions

Smiths Medical ASD, Inc.

FDA Devices Moderate Apr 16, 2014

PCP Test Card; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Methamphetamine Strip; LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

5X250 MM Curved Cannula, Arm 2 for use with daVinci SI Surgical System, model number IS3000. Intuitive Surgical 1266 Kifer Road Sunnyvale, CA 94086 The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians in an operating room environment for endoscopic manipulation of tissue, grasping, cutting, blunt and sharp dissection, approximation,clip- ligation, electrocautery and suturing

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 16, 2014

Propoxyphene Test Strip; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Syphilis Test Card Whole Blood(Serum) LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Syphilis Test Card (Serum); LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

CK-MB Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Drugs of Abuse Panel Test Device; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Morphine Test Card (2000); LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Alcohol Test, Saliva; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Sit/stand Rolling Walker, SKU/Item Number 66838. Intended for use by those with difficulty walking and weighing 225 lbs. or less.

Central Purchasing LLC DBA Harbor Freight Tools

FDA Devices Moderate Apr 16, 2014

Salmonella typhi IgG/IgM Duo Test; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

5X300 MM Curved Cannula, Arm 1 for use with daVinci SI Surgical System, model number IS3000. Intuitive Surgical 1266 Kifer Road Sunnyvale, CA 94086 The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians in an operating room environment for endoscopic manipulation of tissue, grasping, cutting, blunt and sharp dissection, approximation,clip- ligation, electrocautery and suturing

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 16, 2014

Troponin I test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Myoglobin Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

K2 (synthetic Marijuana) Test card; LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Benzodiazepine Test Card; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

7mm Drain Kit Flat 3/4 Perforated with 100ml S-Vac Bulb Evacuator, Sterile (10/case) 10 FR Drain Kit 3/4 Fluted with Trocar and 100ml S-Vac Bulb Sterile (10/case) 10mm Drain Kit, Flat Full Perforated with Trocar, Saber 100ml Bulb and 3C System Sterile (10/case)

Aspen Surgical Products, Inc.

FDA Devices Moderate Apr 16, 2014

Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofragmentation.

Alcon LenSx, Inc.

FDA Devices Moderate Apr 16, 2014

GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, Non-Sterile, DePuy, Johnson & Johnson Product Usage: Usage: The GLOBAL APG+ 2.5mm Guide Pin is a single-use instrument that is used to assist the surgeon in the orientation of the cannulated reamer(s) and cannulated central drills in the preparation of the glenoid surface. The GLOBAL APG+ 2.5mm Guide Pin is validated for use with the GLOBAL APG+, GLOBAL STEPTECH APG, and DELTA XTEND Systems. The guide pin

DePuy Orthopaedics, Inc.

FDA Devices Moderate Apr 16, 2014

Cardiac Panel Test (Serum); LumiQuick,. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Fecal Occult Blood Test Card; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

Barbiturate Test Card; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

7mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case) Intended for closed wound suction drainage

Aspen Surgical Products, Inc.

FDA Devices Moderate Apr 16, 2014

MDMA/Ecstasy Strip; LumiQuick. Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

K-Lite Knee 2 Stays with Visco, Model No. 122015. Product Usage: The product is intended to provide flexible knee support.

Breg Inc

FDA Devices Moderate Apr 16, 2014

Malaria pan Antigen Test; LumiQuick, Santa Clara, CA 95054

LumiQuick Diagnostics Inc.

FDA Devices Moderate Apr 16, 2014

15FR Drain Kit Full Fluted with Trocar and 100ml S-Vac Bulb, Sterile (10/case) Intended for closed wound suction drainage

Aspen Surgical Products, 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.