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 9 critical, 40 moderate, and 1 lower-severity recalls. The page references 35 distinct recalling firms operating in 8 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), CPSC (10), FDA Food (10), 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 Nov 18, 2015

GE Healthcare, SIGNA HDxt 3.0T. Product Usage: The 1.5T Signa HDx family and 3.0T Signa HDx family are a whole body magnetic resonance scanner for use as a diagnostic imaging device.

GE Healthcare

FDA Devices Moderate Nov 18, 2015

MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Nov 18, 2015

GE Healthcare, SIGNA HD 3.0T. Product Usage: The Signa Profile EXCITE MR system is an open, whole body scanner for use as a diagnostic imaging device. It may be utilized for imaging during interventional procedures when performed with MR compatible devices such as in-room display and MR safe biopsy needles.

GE Healthcare

FDA Devices Moderate Nov 18, 2015

Access CEA Assay, Part No. 33200. For the quantitative determination of Carcinoembryonic Antigen (CEA) levels in human serum.

Beckman Coulter Inc.

FDA Devices Moderate Nov 18, 2015

miraDry System consisting of the MD4000-MC Console, the MD4000-HP miraDry Handpiece, and the MD4000-BT miraDry bioTip and accessories. General and Plastic Surgery: The miraDry System is intended for the treatment of primary axillary hyperhidrosis and was recently cleared for the permanent removal of underarm hair.

Miramar Labs, Inc.

FDA Devices Moderate Nov 18, 2015

Cook Medical CXI Support Catheter 2.6FR curved catheter and 4.0FR straight catheter, for cardiovascular use.

Cook Inc.

FDA Devices Moderate Nov 18, 2015

Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152 AMP020150152 AMP025120152 AMP030080152 AMP040040152 AMP225210152 AMP020040152 AMP025040152 AMP025150152 AMP030120152 AMP040080152 AMP253210152 AMP020080152 AMP025080002 AMP030040002 AMP030150152 AMP040120152 AMP335210152 AMP020120152 AMP025080152 AMP030040152 AMP035120152 AMP040150152 AMP354210152; OUS: AMD025150152 AMD030150152 AMD040120002 AMD335210002 AMD030040002 AMD035040152 AMD040120152 AMD335210152 AMD03004

Medtronic Vascular, Inc.

FDA Devices Moderate Nov 18, 2015

Synthes Small Notch Titanium Reconstructive Plate set (SNTRP). Ti PLATE/ROD/PLATE 231mm 6HOLES/5.0mm ROD/17HOLES. Orthopedic implant.

Synthes (USA) Products LLC

FDA Devices Moderate Nov 18, 2015

Maquet Getinge Group, Universal Frame for Positioning Patients (1007.24XX) Manufacturer: Maquet GmbH, Germany The MAQUET Adjustable Positioning Elements are designed for the placement and positioning of patients in the prone position immediately before, during and after surgical interventions as well as for examination and treatment. With a patient in the prone position, the adjustable positioning elements stabilize the upper body while simultaneously relieving the abdominal region in the verti

Maquet Cardiovascular Us Sales, Llc

FDA Devices Moderate Nov 18, 2015

GE Healthcare, SIGNA HDx 3.0T. Product Usage: The GE Signa HDx MR system is a whole body magnetic resonance scanner for use as a diagnostic imaging device.

GE Healthcare

FDA Devices Moderate Nov 18, 2015

Stryker Orthopaedics, MIS MODULAR DISTAL CAPTURE TRIATHLON MIS INSTRUMENTS, REF 6541-5-723, Lot AdminECR19205, Non-Sterile, The Triathlon MIS Distal Capture is used when a surgeon elects to use a capture for the distal femoral resection in a Triathlon primary MIS TKA. Once the Triathlon MIS distal Resection Guide (cat. no. 6541-5-721/722, for left or right preparation, respectively) has been secured to the femoral, the MIS distal capture can optionally be attached to the distal resection guide t

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Nov 18, 2015

Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.

Teleflex Medical

FDA Devices Moderate Nov 18, 2015

NovoCut Suture Manager; Ceterix catalog number CTX-001. General and Plastic Surgery: Intended for use in arthroscopic surgery.

Ceterix Orthopedics, Inc.

FDA Devices Moderate Nov 18, 2015

Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Nov 18, 2015

DeRoyal Sterile Custom Surgical Kits containing 3M DuraPrep (TM) Surgical Solution, Catalog No. 8630, Lot Nos: 2016-09EE: TOTAL KNEE A & B, REF 89-4561.11; TOTAL HIP A & B, REF 89-4562.12; PODIATRY TRAY, REF 89-3101.04; KNEE SCOPE PACK, REF 89-7744.03; KNEE PACK, REF 89-8194.02; BEACH CHAIR PACK, REF 89-8439.01; TOTAL JOINT, REF 50-12160.17; BACK TRAY, REF 50-12602.09; PACEMAKER PACK, REF 89-8381.01;

DeRoyal Industries Inc

FDA Devices Moderate Nov 18, 2015

Maquet Getinge Group, Adjustable Positioning Elements (1007.28A0) Manufacturer: Maquet GmbH, Germany. Patient positioners. The MAQUET Adjustable Positioning Elements are designed for the placement and positioning of patients in the prone position immediately before, during and after surgical interventions as well as for examination and treatment. With a patient in the prone position, the adjustable positioning elements stabilize the upper body while simultaneously relieving the abdominal regio

Maquet Cardiovascular Us Sales, Llc

FDA Devices Moderate Nov 18, 2015

R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip, Sterile, Rx only, Teleflex Medical.

Teleflex Medical

FDA Devices Moderate Nov 18, 2015

GE Healthcare, SIGNA PET/MR 3.0T. Product Usage: The SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high-resolution physiologic and anatomic information, acquired simultaneously and isocentrically.

GE Healthcare

FDA Devices Moderate Nov 18, 2015

Samsung GM60A-40S Intended for use in generating radiographic images of human anatomy.

NeuroLogica Corporation

FDA Devices Moderate Nov 18, 2015

Focus Diagnostics Anaplasma Phagocytophilum IFA IgM Test Kit, Model No. IF1450M in vitro diagnostic.

Focus Diagnostics Inc

FDA Devices Moderate Nov 18, 2015

GE Healthcare, SIGNA 3.0T. Product Usage: Magnetic resonance system for diagnostic imaging. The indications for use for the 3.0T Signa VH/i (Signa 3.0T MR System) Transmit/Receive Body Imaging Coil expands the imaging capability of the 3.0T Signa VH/i MR Imaging System. The Transmit/Receive Body Imaging Coil is intended for imaging of the Neck, Spine, Abdomen/Thorax and the extremities.

GE Healthcare

FDA Devices Low Nov 18, 2015

MILEX PESSARY KIT; Model Numbers: MXPES00; MXKPES00; MXKPREG03; MXKPGSK07 Product Usage: The Coopersurgical MILEX SILICONE PESSARY is used to manage a number of gynecologic issues including pelvic support defects and stress urinary incontinence.

CooperSurgical, Inc.

FDA Devices Moderate Nov 18, 2015

Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drilling unit to carry components such as implant mounts, healing abutments and screws for placement and removal. For dental and restorative procedures.

Biomet 3i, LLC

FDA Devices Moderate Nov 18, 2015

Myelo-Nate CSF Sampling Kit, Neonatal/Pediatric cerebralspinal fluid sampling sterile tray, including a lumbar puncture needle, four collection vials, an iodine swabstick package, a fenestrated drape, a polylined drape, three gauze pads, and one spot bandage.

Utah Medical Products, Inc

FDA Devices Moderate Nov 18, 2015

Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips are attached to a surgical drilling unit to carry components such as implant mounts, healing abutments and screws for placement and removal. For dental and restorative procedures.

Biomet 3i, LLC

FDA Devices Moderate Nov 18, 2015

TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811

Tekia, Inc.

CPSC No agency class Nov 17, 2015

Kona Recalls Bicycles Due to Fall Hazard

Kona Bicycle Company, of Ferndale, Wash.

CPSC No agency class Nov 17, 2015

PetSmart Expands Recall of Fish Bowls Due to Laceration Hazard

Shanghai Freeart Trading Co. Ltd., of China

CPSC No agency class Nov 17, 2015

PetSmart Recalls Top Fin Betta Bowl Kits Due to Laceration Hazard

CPSC No agency class Nov 17, 2015

REI Recalls Outdoor Rocker Chairs Due to Fall Hazard

NHTSA No agency class Nov 17, 2015

FORD 2006-2014: EQUIPMENT ADAPTIVE/MOBILITY

FORD

USDA FSIS Moderate Nov 17, 2015

Tyson Foods Inc. Recalls Chicken Product Due To Possible Adulteration

Tyson Foods, Inc.

NHTSA No agency class Nov 16, 2015

HYUNDAI 2011-2012: EXTERIOR LIGHTING:BRAKE LIGHTS:SWITCH

HYUNDAI

NHTSA No agency class Nov 16, 2015

HYUNDAI 2013-2015: SUSPENSION:REAR

HYUNDAI

CPSC No agency class Nov 12, 2015

Family Dollar Recalls Wax Warmers Due to Fire and Burn Hazards

CPSC No agency class Nov 12, 2015

Laceration Injuries Prompt SharkNinja to Recall Ninja BL660 Blenders to Provide New Warnings and Instructions

Hai Xin Technology (Shenzhen) Co. Ltd., Shenzhen, China

CPSC No agency class Nov 12, 2015

Mahindra USA Recalls Compact Tractors Due to Fire Hazard (Recall Alert)

CPSC No agency class Nov 12, 2015

PNY Recalls Portable Lithium Polymer Battery Packs Due to Fire Hazard

PNY Technologies, Inc., of Parsippany, N.J.

CPSC No agency class Nov 12, 2015

STIHL Recalls Edgers, Trimmer/Brushcutters, Pole Pruners and KombiMotors Due to Fire Hazard

STIHL Inc., of Virginia Beach, Va.

CPSC No agency class Nov 12, 2015

WakaWaka Recalls Adapter Kits Due to Electrical Shock, Explosion, Fire Hazards (Recall Alert)

FDA Food Critical Nov 11, 2015

ON THE BORDER MEXICAN GRILL & CANTINA Cafe Style Tortilla Chips 18 oz. bags

Shearer's Foods Inc.

FDA Food Critical Nov 11, 2015

AKSAR (life taste and beyond) Cashew Pieces 4040615 Net Wt: 7oz (200gm) , Net Wt: 28oz (800gm) 4051315 Net Wt: 400 gms (14oz) , Net Wt: 5lb 20 NEWLAND COURT, STERLING, VA 20165 Phone # 703-880-9802 , FAX # 703-880-1602

Aksar LLC

FDA Food Moderate Nov 11, 2015

Krispy Kreme Doughnuts, Chocolate Iced Doughnuts with Kreme Filling, 2 count, Net Wt. 4.65oz, and Half Dozen, Net Wt. 16.2 oz., Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston Salem, NC 27102.

Krispy Kreme Doughnut Corporation

FDA Food Critical Nov 11, 2015

Organic Coriander Powder (Dhania Powder), 60packs/case, UPC 40074 13813

Nijay International, Inc.

FDA Food Moderate Nov 11, 2015

Krispy Kreme Doughnuts, Glazed Lemon Filled Doughnuts, (2 count, Net Wt. 4.65oz and Half Dozen, Net Wt. 16oz), Manufactured under the authority of Krispy Kreme Doughnut Corporation, Winston Salem, NC 27102.

Krispy Kreme Doughnut Corporation

FDA Food Moderate Nov 11, 2015

Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc., Paterson, New Jersey 07544 UPC 0-32394-7027-7 #70271

Kontos Foods Inc.

FDA Food Critical Nov 11, 2015

Naturipe Foods Frozen Blueberries, IQF, 30 lb. boxes and 1500 lb. Totes, packed in cardboard boxes with plastic bag liners; 50 boxes per pallet or 1 Tote per pallet

MBG Marketing

FDA Food Critical Nov 11, 2015

Nature's Eat Natural Macadamia Nuts NET WT 6 OZ (170g) in cello bags.

Texas Star Nut and Food Co., Inc.

FDA Food Critical Nov 11, 2015

Earth Exotic Brussels Sprouts Net. Wt. 8 oz. (227 g) Net. Wt. 32 oz (2 LBS) 907 g

A.M.S. Exotic Llc

FDA Food Critical Nov 11, 2015

Spicy Mix Hydroponic Micro Greens packaged in 2 oz. plastic hinged clamshell

Hilltop Farm

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.