PlainRecalls

2017 Recalls

7,536 recalls · Page 80 of 151

2017 Recall Year Insight

Federal agencies issued 7,536 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.41% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 20.6 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 151 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 2017.

On this page of 50 records, severity classification shows 14 critical, 33 moderate, and 3 lower-severity recalls. The page references 33 distinct recalling firms operating in 7 distinct product categories, with 39 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (24), FDA Food (12), NHTSA (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 2017 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 Low Jun 7, 2017

AIA-PACK TPOAb CONTROL SET

Tosoh Bioscience, Inc.

FDA Devices Moderate Jun 7, 2017

1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Systems (Part Number M8275093/5). The InfoV.A.C. and V.A.C.ULTA Negative Pressur…

KCI USA, INC.

FDA Devices Moderate Jun 7, 2017

AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

AbbVie Inc.

FDA Devices Moderate Jun 7, 2017

Her2/Neu (EP3); 0.5 mL Catalog number 237R-25; 1.0 mL Catalog number 237R-26; 7.0 mL Catalog number 237R-28. Immunology - Analyte Specific Reag…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 mL Catalog number362A-18 . Microbiology - Analyte Specific Reagent In vitro diagnosti…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F

Toshiba American Medical Systems Inc

FDA Devices Moderate Jun 7, 2017

AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail System is intended to treat stable and unstable proximal fractures of the femur in…

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 7, 2017

Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems

GE Healthcare, LLC

FDA Devices Moderate Jun 7, 2017

Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000

Cardinal Scale Mfg Co

FDA Devices Moderate Jun 7, 2017

Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with a…

Zimmer Biomet, Inc.

FDA Devices Low Jun 7, 2017

AIA-PACK TgAb CONTROL SET

Tosoh Bioscience, Inc.

FDA Devices Moderate Jun 7, 2017

Elecsys PreciControl Varia 3

Roche Diagnostics Corporation

FDA Devices Moderate Jun 7, 2017

Adenovirus (20/11 & 2/6); 0.5 mL Catalog # 212M-15; and 7.0 mL Catalog number 212M-18 Microbiology - Analyte Specific Reagent In vitro diagno…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

CD117, c-kit (YR145) 1.0 ml catalog number 117R-16 7.0 ml catalog number-18 Microbiology - Analyte Specific Reagent In vitro diagnostic use - A…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 7, 2017

Arrow(R) VPS(R) Access Kit for use with 4 and 5 Fr. Peripherally Inserted Central Venous Catheters

Arrow International Inc

FDA Devices Moderate Jun 7, 2017

Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model Number(s): L7572. For the in vitro quantitative kinetic determination of lact…

Medtest Holdings, Inc.

FDA Devices Moderate Jun 7, 2017

SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers-For the quantitative measurement of SH…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Critical Jun 7, 2017

Absorb Bioresorbable Vascular Scaffold (BVS) system (Australia). The Absorb BVS is a temporary scaffold indicated for improving coronary luminal dia…

Abbott Vascular

FDA Devices Moderate Jun 7, 2017

Draco Enzymatic Deep-Cleaning Pad with Enzymatic Detergent Catalogue Number: HY0305Z

Madison Polymeric Engineering

FDA Devices Moderate Jun 7, 2017

Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Estrogen Receptor (EP1) 7.0 mL Catalog number 249R-28; 1.0 mL Catalog number 249R-16 Microbiology - Analyte Specific Reagent In vitro diagno…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Her2/Neu (c-erbB-2) (CB-1 1); 7.0 mL Catalog number 237M-18. In vitro diagnostic use - Analyte Specific Reagent Immunology - Analyte Specific Re…

Cell Marque Corporation

CPSC Moderate Jun 7, 2017

Lithonia Lighting Recalls to Repair Ceiling Light Fixtures Due to Impact Hazard

Lithonia Lighting, a division of Acuity Brands Lighting Inc., of Conyers, Ga.

CPSC Moderate Jun 7, 2017

Madison Mill Recalls Safety Gates Due to Entrapment and Strangulation Hazards

Madison Mill Inc., of Ashland City, Tenn.

CPSC Moderate Jun 7, 2017

Nidec Motor Recalls Swimming Pool Motors Due to Electrical Shock Hazard

Nidec Motor Corp., of St. Louis, Mo.

NHTSA Critical Jun 7, 2017

PORSCHE 2010-2012: ENGINE

PORSCHE

CPSC Moderate Jun 6, 2017

Arctic Cat Recalls Snowmobiles Due to Impact Hazard (Recall Alert)

Arctic Cat Inc., of Thief River Falls, Minn.

CPSC Moderate Jun 6, 2017

Lila + Hayes Recalls Children's Playwear Due to Choking Hazard

NHTSA Moderate Jun 5, 2017

HYUNDAI 2017: SEAT BELTS:FRONT:ANCHORAGE

HYUNDAI

NHTSA Critical Jun 5, 2017

MERCEDES-BENZ 2016: EQUIPMENT:OTHER:LABELS

MERCEDES-BENZ

NHTSA Critical Jun 5, 2017

HYUNDAI 2015-2016: PARKING BRAKE:INDICATOR LIGHT

HYUNDAI

NHTSA Critical Jun 5, 2017

HYUNDAI 2013-2017: LATCHES/LOCKS/LINKAGES:HOOD:LATCH

HYUNDAI

CPSC Moderate Jun 1, 2017

Kreative Kids Recalls Children's Robes Due to Violation of Federal Flammability Standard

Kreative Kids Inc., of Pomona, Calif.

NHTSA Critical Jun 1, 2017

TOYOTA 2016-2017: ENGINE

TOYOTA

NHTSA Critical Jun 1, 2017

MAZDA 2004: SUSPENSION:FRONT:CONTROL ARM:LOWER ARM

MAZDA

NHTSA Critical Jun 1, 2017

MAZDA 2004-2008: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP

MAZDA

FDA Food Critical May 31, 2017

Slow Roasted Ham & Swiss Breakfast Sandwich, Fully Cooked/Keep Frozen/Perishable Net Wt 5.6 oz (159 g) MANUFACTURED EXCLUSIVELY FOR STARBUCKS COFFEE …

SK Food Group Groveport

FDA Food Moderate May 31, 2017

Sugar Crackers 400g (14.1oz) x 12 packets per carton/case, UPC 9556184 500023

U-Can Food Trading Inc

FDA Food Moderate May 31, 2017

7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 1267 4, NET CASE WT 12.9 KG (28 LB 7 OZ), UNIT NET WT: 198 G (7 OZ), COUNT: 65 --- PROCESSE…

Rich Products Corp

FDA Food Critical May 31, 2017

Nutty INFUSIONS Roasted Cashew Butter, NET WT. 10 OZ (284 g)

HVF Inc. d.b.a Huson Valley Farms

FDA Food Moderate May 31, 2017

Bean Sprout 10 lbs. bag, 10lb box, 12/12oz, 20/15oz, 24/1.5 lbs., 5lbs. bag, 3lb tray

Fuji Natural Foods, Inc.

FDA Food Moderate May 31, 2017

ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 00 49800 11413 2, NET CASE WT: 27 LB (12.2 KG), UNIT NET WT: 18 OZ (1 LB 2 OZ) (510G), COU…

Rich Products Corp

FDA Food Critical May 31, 2017

Nutty INFUSIONS Ginger Wasabi Cashew Butter, NET WT. 10 OZ (284 g)

HVF Inc. d.b.a Huson Valley Farms

FDA Food Low May 31, 2017

Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-118…

RB Manufacturing LLC

FDA Food Critical May 31, 2017

Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103 www.homemadegourmet.com

Phoenix Food, LLC

FDA Food Critical May 31, 2017

Herbal Tea Variety 120 ml/pouch, 40 pouches/case

U S Deer Antlers Export & Import

FDA Food Moderate May 31, 2017

ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA DOUGH BALL, RICH'S label, Produ…

Rich Products Corp

FDA Food Critical May 31, 2017

Organic Veda brand Ginger Powder, 24 jars, Net Wt. 16 oz. (454 grams)

Lords Organics Llc

Nearby Recall Years

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

Compare 2017 with 2016 →

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 2017

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2017 across the FDA, CPSC 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 August 2026.