PlainRecalls

2015 Recall Year Insight

Federal agencies issued 8,173 product recalls indexed by PlainRecalls in calendar year 2015. That represents about 7.83% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 22.4 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 164 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 2015.

On this page of 50 records, severity classification shows 18 critical, 32 moderate, and 0 lower-severity recalls. The page references 32 distinct recalling firms operating in 8 distinct product categories, with 36 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (21), NHTSA (14), CPSC (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 2015 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 Dec 23, 2015

MiniMed 640G, 3.0mL mmol/L, 3.0mL mg/dL, Model No. MMT-1711 and MMT-1712 The MiniMed 620G and MiniMed 640G insulin pump systems are indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. In addition, the pump system is indicated for continuous monitoring of glucose levels in the fluid under the skin, and possible low and high blood glucose episodes.

Medtronic MiniMed Inc.

FDA Devices Moderate Dec 23, 2015

Digital Temple Thermometer labeled under: Bestmed, Good Neighbor (Amerisource Bergen), Kroger, Medline, Meijer, Premier Value, Safeway, Life Brand, Target, Top Care, Best Choice, Western Family. Device is packaged in plastic blister with cardboard insert, 2 AAA batteries installed, a Quick Start Guide, and an Instruction Manual booklet. Product Usage: Device is a handheld thermometer that employs a thermistor sensor intended for people to take a human body temperature at the temporal artery

Bestmed, LLC

FDA Devices Moderate Dec 23, 2015

MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).

bioMerieux, Inc.

FDA Devices Moderate Dec 23, 2015

MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).

bioMerieux, Inc.

FDA Devices Moderate Dec 23, 2015

Fujifilm Medical Systems Duodenoscope, Model Numbers ED-200XU, ED-200XT, ED-250XT, ED-310XU, ED-420XL, ED-410XT, ED-410XU, ED-450XL, and ED-450XT. Medical endoscope for the duodenum and upper G.I. tract. Open elevator wire channel duodenoscopes.

Fujifilm Medical Systems U.S.A., Inc.

FDA Devices Moderate Dec 23, 2015

VentriClear¿ II Ventricular Drainage Catheter Set. Allows external access and drainage of cerebrospinal fluid (CSF) from the ventricles of the brain.

Cook Inc.

FDA Devices Moderate Dec 23, 2015

UniCel DxH 600 Coulter Cellular Analysis System, Software Version 1.1.1.0, Part No. B23858 The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a whole-blood sample, smears a blood film on a clean microscope slide, and delivers a variety of fixatives, stains, buffers, and rinse solutions to that blood smear.

Beckman Coulter Inc.

FDA Devices Moderate Dec 23, 2015

MiniMed 620G, 3.0mL mg/dL, Model No. MMT-1710 The MiniMed 620G and MiniMed 640G insulin pump systems are indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. In addition, the pump system is indicated for continuous monitoring of glucose levels in the fluid under the skin, and possible low and high blood glucose episodes.

Medtronic MiniMed Inc.

FDA Devices Critical Dec 23, 2015

OmniPod¿, Insulin Management System (US) Catalog Number: PODZXP420 Product Usage: The OmnniPod¿ Insulin Management System is intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin and for the quantitative measurement of glucose in fresh whole capillary blood (in vitro) from the finger.

Insulet Corporation

FDA Devices Moderate Dec 23, 2015

Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column

Teleflex Medical

FDA Devices Moderate Dec 23, 2015

Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system

Philips Electronics North America Corporation

FDA Devices Moderate Dec 23, 2015

Philips Healthcare Ingenuity CT Computed Tomography X-ray system

Philips Electronics North America Corporation

FDA Devices Moderate Dec 23, 2015

Intravascular (IV) Administration Sets, Model No. 54IV12, 54IV22, 54IV32, MK2450, 54IV42, MK132, MK2156, MK2270, MK2292, MK2300, MK2374, MK2394, MK2508, MK2227

Edwards Lifesciences, LLC

FDA Devices Moderate Dec 23, 2015

Philips Healthcare Brilliance 64 Computed Tomography X-ray system

Philips Electronics North America Corporation

FDA Devices Critical Dec 23, 2015

Perseus A500 Anesthesia Workstation, MK06000. Intended for use in anesthetizing adults, children, and neonates and can be used for automatic and manual ventilation, pressure-supported spontaneous breathing, and spontaneous breathing.

Draeger Medical, Inc.

FDA Devices Moderate Dec 23, 2015

Catalog No. INF0020-A  EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Connector (spiked set); Catalog No. INF0500-A - 500ml EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Connector; Catalog No INF1200-A - 1200ml EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Connector; Catalog No GR1200-A  1200ml Enteral Feeding Delivery Set with ENFit Conn

MOOG Medical Devices Group

FDA Devices Moderate Dec 23, 2015

GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4 - 0574-0001; GVL 5- 0574-0030. The system consists of a video laryngoscope and portable video monitor. The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a clear, unobstructed view of the vocal cords for medical procedures. GVL is a video laryngoscope that incorporates a high resolution color camera, an LED light source and video output to a remote monitor.

Verathon, Inc.

FDA Devices Moderate Dec 23, 2015

MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).

bioMerieux, Inc.

FDA Devices Moderate Dec 23, 2015

MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the instruments connected to the application and the LIS(s) (Laboratory Information System(s)).

bioMerieux, Inc.

FDA Devices Moderate Dec 23, 2015

UniCel DxH 800 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 629029, B24465, B24802 The UniCel DxH 800/DxH 600 analyzers are quantitative, multi-parameter, automated hematology analyzers for in vitro diagnostic use in screening patient populations found in clinical laboratories. The DxH 800 is available as an analyzer for use on a benchtop or with a floor stand. The DxH 600 is available as an analyzer for use on a benchtop only.

Beckman Coulter Inc.

FDA Devices Moderate Dec 23, 2015

GE Healthcare Optima CL323i Product Usage: The angiographic X-ray systems are indicated for use for patients from newborn to geriatric in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventional procedures. Additionally, with the OR table, the angiographic X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for image-guided surgical procedures. The OR table is

GE Medical Systems, LLC

NHTSA No agency class Dec 23, 2015

JEEP 2015: STEERING:HYDRAULIC POWER ASSIST:HOSE, PIPING, AND CONNECTIONS

JEEP

NHTSA No agency class Dec 23, 2015

CHEVROLET 2015: SEAT BELTS:FRONT:ANCHORAGE

CHEVROLET

NHTSA No agency class Dec 23, 2015

HONDA 2011-2013: ELECTRICAL SYSTEM:WIRING

HONDA

NHTSA No agency class Dec 23, 2015

HYUNDAI 2011-2012: ELECTRONIC STABILITY CONTROL (ESC)

HYUNDAI

CPSC No agency class Dec 22, 2015

Breville Recalls Pressure Cookers Due to Risk of Burns

Breville USA Inc., of Torrance, Calif.

CPSC No agency class Dec 22, 2015

Carrier Recalls to Repair Packaged Terminal Air Conditioners, Heat Pumps Including Previously Recalled Units Due to Fire Hazard

Carrier Corporation, of Farmington, Conn.

CPSC No agency class Dec 22, 2015

John Deere Recalls Zero Turn Lawn Mowers Due to Risk of Fire, Serious Injury or Death (Recall Alert)

Deere & Company, of Moline, Ill.

CPSC No agency class Dec 22, 2015

Victorian Trading Company Recalls Tealight Holders Due to Fire Hazard (Recall Alert)

NHTSA No agency class Dec 22, 2015

FORD 2015: SEAT BELTS:FRONT:ANCHORAGE

FORD

NHTSA No agency class Dec 22, 2015

FORD 2015: POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT

FORD

NHTSA No agency class Dec 22, 2015

HYUNDAI 2015: TIRES:SIDEWALL

HYUNDAI

NHTSA No agency class Dec 22, 2015

FORD,MERCURY 2003-2005: EXTERIOR LIGHTING:HEADLIGHTS

FORD,MERCURY

NHTSA No agency class Dec 22, 2015

FREIGHTLINER,WESTERN STAR 2015-2016: POWER TRAIN:AXLE ASSEMBLY

FREIGHTLINER,WESTERN STAR

NHTSA No agency class Dec 22, 2015

FORD 2016: SERVICE BRAKES, AIR:SUPPLY:HOSES, LINES/PIPING, AND FITTINGS

FORD

USDA FSIS Moderate Dec 22, 2015

Bellisio Foods, Inc. Recalls Boneless Pork Rib Frozen Entree Products Due To Possible Foreign Matter Adulteration

Bellisio Foods, Inc.

USDA FSIS Critical Dec 19, 2015

The Cure House Recalls Pork Products Produced Without Benefit Of Inspection

NHTSA No agency class Dec 18, 2015

SUZUKI 2014: ELECTRICAL SYSTEM:IGNITION

SUZUKI

NHTSA No agency class Dec 18, 2015

SUZUKI 2014: ELECTRICAL SYSTEM:12V/24V/48V BATTERY:CABLES

SUZUKI

NHTSA No agency class Dec 18, 2015

SUZUKI 2012-2013: ENGINE AND ENGINE COOLING:ENGINE

SUZUKI

NHTSA No agency class Dec 18, 2015

SUZUKI 2014: ELECTRICAL SYSTEM:WIRING

SUZUKI

USDA FSIS Critical Dec 18, 2015

Bonavista Foods Inc. Recalls Pork Products Produced Without Benefit Of Import Inspection

Bonavista foods Inc.

CPSC No agency class Dec 17, 2015

Ace Bayou Reannounces Recall of Bean Bag Chairs Due to Low Rate of Consumer Response; Two Child Deaths Previously Reported; Consumers Urged to Install Repair

Ace Bayou Corp., of New Orleans, La.

CPSC No agency class Dec 17, 2015

Casablanca Recalls Ceiling Fans Due to Injury Hazard

CPSC No agency class Dec 17, 2015

Focus Bicycles Recalls Izalco Max Bicycles Due to Fall Hazard

CPSC No agency class Dec 17, 2015

S.R. Smith Recalls Pool Lifts Due to Fall Hazard

S.R. Smith, LLC, of Canby, Ore.

FDA Food Moderate Dec 16, 2015

Canned Chinook Salmon with paper label reading in part: ***SKIPANON BRAND SEAFOOD CHINOOK SALMON***Ingredients: Chinook Salmon, Sea Salt NET WT. 6 OZ. (170g)***" UPC: 58071 00118 Can code beginning with OCCR. Label background is yellow with a brown stripe at the bottom and multiple colored ink lettering. Chinook (aka King) Salmon with salt added, canned and distributed as brites in 6oz cans. Can code beginning with OCCR.

Skipanon Brand Seafoods LLC

FDA Food Moderate Dec 16, 2015

SMOKED ALBACORE TUNA, sold under brand The Garibaldi Cannery, metal can, net weight 8 oz. (227 gram). No UPC

The Garibaldi Cannery, LLC

FDA Food Moderate Dec 16, 2015

Albacore Tuna in gold pouches with stick-on label reading in part: ***SKIPANON BRAND SEAFOOD ALBACORE TUNA***INGREDIENTS: Albacore Tuna, Sea Salt. NET WT. 48 OZ. ***" UPC: 58071 00148 Code on pouch beginning with OCK TUNA 3#. Label has green, yellow and blue background with multiple color lettering. Canned Albacore Tuna with paper label reading in part: ***SKIPANON BRAND SEAFOOD ALBACORE TUNA***Ingredients: Albacore Tuna, Sea Salt. NET WT. 66.5 OZ. (1885g)***" UPC: 58071 00144 C

Skipanon Brand Seafoods LLC

FDA Food Moderate Dec 16, 2015

Texas Style HEB Charro Beans Spicy NET WT. 15 OZ (425g) in metal cans UPC: 041220927159.

Durrset Amigos Ltd.

Nearby Recall Years

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

Compare 2015 with 2014 →

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 2015

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 2015 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.