PlainRecalls

2016 Recalls

6,806 recalls · Page 86 of 137

2016 Recall Year Insight

Federal agencies issued 6,806 product recalls indexed by PlainRecalls in calendar year 2016. That represents about 8.11% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 18.6 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 137 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 2016.

On this page of 50 records, severity classification shows 12 critical, 38 moderate, and 0 lower-severity recalls. The page references 37 distinct recalling firms operating in 7 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), NHTSA (10), CPSC (9), 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 2016 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance iCT Computed Tomography X-Ray System

Philips Healthcare

FDA Devices Moderate Jun 15, 2016

Stryker FlowPort II Adapter: Model number: 00CAT00778 The FlowPort II Adapter is intended to connect the FlowPort II Cannulas to commercially avail…

Stryker Corporation

FDA Devices Moderate Jun 15, 2016

Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products.

Ellipse A/S

FDA Devices Moderate Jun 15, 2016

VITROS 3600 Immunodiagnostic System, Catalog Number 6802783,for use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a…

Ortho-Clinical Diagnostics

FDA Devices Moderate Jun 15, 2016

Philips Healthcare DuraDiagnost stationary X-ray system

Philips Healthcare

FDA Devices Moderate Jun 15, 2016

Cholesterol, Catalog No. OSR6x16 Product Usage:Cholesterol OSR6x16 is intended as a System reagent for the quantitative determination of Cholester…

Beckman Coulter Inc.

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance 64 Computed Tomography X-Ray System

Philips Healthcare

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Brilliance iCT SP Computed Tomography X-Ray System

Philips Healthcare

FDA Devices Moderate Jun 15, 2016

Medtronic RestoreSensor, Model 37714; and, RestoreSensor SureScan, (MRI), Model 97714, Implantable Neurostimulators. Used to treat chronic, intrac…

Medtronic Neuromodulation

FDA Devices Moderate Jun 15, 2016

Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Laser Products.

Ellipse A/S

FDA Devices Moderate Jun 15, 2016

Norian Drillable Inject 10 CC-Sterile; catalog # 07.704.010S Intended for bony voids or defects of the extremities and pelvis that are not instrinsi…

Synthes (USA) Products LLC

FDA Devices Moderate Jun 15, 2016

The Plum A+ is a dual-line volumetric infusion system designed to meet the growing demand for hospital-wide, as well as alternate site and home healt…

Hospira Inc.

FDA Devices Moderate Jun 15, 2016

Sedecal SA Mobile Diagnost w DR x-ray system

Sedecal USA, Inc.

FDA Devices Moderate Jun 15, 2016

Oxoid Nitrocefin (+ Reconstitution Fluid Batch) REF: SR0112C, Oxoid Ltd. For the rapid chromogenic detection of beta-lactamase activity in bacterial…

Remel Inc

FDA Devices Moderate Jun 15, 2016

Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joi…

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 15, 2016

Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection

Becton Dickinson & Company

FDA Devices Moderate Jun 15, 2016

Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex Incorporated. A tracheal tub…

Teleflex Medical

FDA Devices Moderate Jun 15, 2016

The Plum 360 is a large volume infuser capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions. Th…

Hospira Inc.

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Elite Computed Tomography X-Ray System

Philips Healthcare

FDA Devices Moderate Jun 15, 2016

Lipase, Catalog No. OSR6x30 Product Usage: Lipase OSR6x30 is intended as a System reagent for the quantitative determination of Lipase activity i…

Beckman Coulter Inc.

FDA Devices Moderate Jun 15, 2016

Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System

Philips Healthcare

FDA Devices Moderate Jun 15, 2016

Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical instrument system. The pne…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jun 15, 2016

DePuy Synthes 8.0 mm Flexible Shaft Reamer, 360 mm, Orthopedic manual surgical instrument. Part number 351.43

Synthes (USA) Products LLC

FDA Devices Moderate Jun 15, 2016

GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. The system is intended …

GE Healthcare, LLC

FDA Devices Moderate Jun 15, 2016

Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional accessory to the Operon Surgical Table. The pads may be attached to the base sec…

Berchtold Corp.

FDA Devices Moderate Jun 15, 2016

Signature TKA GDE/MDL Set 04-05 Patient-specific surgical guide and instrument set.

Materialise USA LLC

FDA Devices Moderate Jun 15, 2016

1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate …

Synthes (USA) Products LLC

CPSC Moderate Jun 15, 2016

Sony Recalls VAIO Laptop Computer Battery Packs Due to Burn and Fire Hazards

SANYO ENERGY (Suzhou) CO, Ltd. of China, Panasonic subsidiary

NHTSA Critical Jun 15, 2016

MERCEDES-BENZ 2016: ELECTRICAL SYSTEM:SOFTWARE

MERCEDES-BENZ

NHTSA Critical Jun 15, 2016

MERCEDES-BENZ 2016: STEERING:ELECTRIC POWER ASSIST SYSTEM

MERCEDES-BENZ

NHTSA Critical Jun 15, 2016

NISSAN 2016: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

NISSAN

CPSC Moderate Jun 14, 2016

Direct Distributors Recalls Angle Grinders Due to Risk of Laceration

CPSC Moderate Jun 14, 2016

Grand Rapids Chair Recalls Chairs and Barstools Due to Risk of Injury (Recall Alert)

Grand Rapids Chair Company, of Byron Center, Mich.

CPSC Moderate Jun 14, 2016

STIHL Recalls Battery-Powered Hedge Trimmers Due to Laceration Hazard

VIKING GmbH, of Austria

NHTSA Critical Jun 13, 2016

INFINITI 2014-2016: STEERING:AUTOMATED/ADAPTIVE STEERING

INFINITI

CPSC Moderate Jun 10, 2016

Auldey Toys Recalls Sky Rover Toys Due to Fire Hazard

NHTSA Critical Jun 10, 2016

KENWORTH,PETERBILT 2017: ELECTRICAL SYSTEM:IGNITION:MODULE

KENWORTH,PETERBILT

NHTSA Moderate Jun 10, 2016

MASERATI 2014: POWER TRAIN:AUTOMATIC TRANSMISSION:GEAR POSITION INDICATION (PRNDL)

MASERATI

NHTSA Critical Jun 10, 2016

CHEVROLET 2013-2016: ELECTRICAL SYSTEM:SOFTWARE

CHEVROLET

CPSC Moderate Jun 9, 2016

360 Electrical Recalls Surge Protectors Due to Shock and Fire Hazards

360 Electrical LLC, of Salt Lake City, Utah

CPSC Moderate Jun 9, 2016

AR500 Armor Recalls Level III Body Armor Due to Risk of Gunshot Injury or Death

AR500 Armor, of Phoenix, Ariz.

CPSC Moderate Jun 9, 2016

Far East Brokers Recalls Children’s Chairs and Swings Due to Violation of Federal Lead Paint Standard

Zhejiang Haifu Leisure Products Co. Ltd., of China

CPSC Moderate Jun 9, 2016

Rhino Metals Recalls Handgun Security Safes Due to a Serious Risk of Injury

Rhino Metals Inc., of Caldwell, Idaho

NHTSA Critical Jun 9, 2016

ACURA,HONDA 2015-2016: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY

ACURA,HONDA

NHTSA Critical Jun 9, 2016

FREIGHTLINER 2017: ENGINE AND ENGINE COOLING:ENGINE:DIESEL

FREIGHTLINER

NHTSA Critical Jun 9, 2016

AUDI 2007-2009: VISIBILITY:SUN/MOON ROOF ASSEMBLY

AUDI

FDA Food Critical Jun 8, 2016

Walnut Delights 6 Pack Net Weight: 9 oz. PLU #69690 UPC: 2 69690 20399 7 Giant Eagle, LLC, Pittsburgh, PA

Giant Eagle, Inc.

FDA Food Moderate Jun 8, 2016

Fruit Tartlets, Raspberry flavor, 9 - 0.56oz (16 g) tartlets - Net Wt. 5.1oz (145 g). Manufactured in France. Distributed by Ouhlala Gourmet Corp. …

Ouhlala Gourmet Llc

FDA Food Critical Jun 8, 2016

Kroger SALTED SUNFLOWER KERNELS 6 oz (170g) INGREDIENTS: SUNFLOWER KERNELS, COTTONSEED AND/OR SUNFLOWER OILS, SALT. DISTRIBUTED BY THE KROGER CO CINC…

The Kroger Co

FDA Food Critical Jun 8, 2016

Choice Products Supreme Elixir 32oz.

World's Choice Products

Nearby Recall Years

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

Compare 2016 with 2015 →

Data Sources

  • Source: FDA openFDA Enforcement API — calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2016