PlainRecalls

2017 Recall Year Insight

Federal agencies issued 7,681 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.36% 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 2017.

On this page of 50 records, severity classification shows 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 9 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 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, 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 5, 2017

Regard, Item Number: 800430005, Sterile, LD0499E - C Section Pk - Cabrini

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800415001, Sterile, OR0484A - Shoulder System Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions

Hospira Inc., A Pfizer Company

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800535001, Sterile, LD0620A - C Section - New Braunfels

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880328001, Sterile, HT0759A - Pacemaker Pk - OSU

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Syngo.x, Picture archiving and communication system Syngo via is a software solution intended to be used for viewing, manipulation, communication, and storage of medical images. It can be used as a standalone device or together with a variety of cleared and unmodified syngo based software options. Syngo.via supports interpretation and evaluation of examinations within healthcare institutions, for example, in Radiology, Nuclear Medicine and Cardiology environments. The system is not intended for

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800528002 Sterile, GS0612B - Lap Chole PK - Westover Hills

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800091002, Sterile, LD0692B - C Section - FMOL Lady of Angels

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800417002, Sterile, GY0486B - Laparoscopy Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800562001, Sterile, NU0651A - Neuro - Childrens Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800557001, Sterile, LD0646A - C Section - Childrens Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800414003, Sterile, OR0483C - Total Joint Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Critical Apr 5, 2017

HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9

Philips North America, LLC

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800508004, Sterile, LD0586D - C Section - Jasper

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800414002, Sterile, OR0483B- Total Joint Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800562002, Sterile, NU0651B - Neuro - Childrens Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800326002, Sterile, GS0757B - Major Basin - OSU

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for use in providing diagnostic quality images to aid the physician with diagnosis

AGFA Healthcare Corp.

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800419002, Sterile, GY0488B - D&C Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800524003, Sterile, LD0608C - C Section - Westover Hills

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800410003, Sterile, CV0479C - Open Heart PK - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800533001, Sterile, GS0606A - Abdominal Pk - Westover Hills

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880323001, Sterile, LD0754A - C Section - OSU

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800422003, Sterile, OR0491C - Arthroscopy Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800036005, Sterile, LD0274E - C Section Pack - FMOL St Francis

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800558004, Sterile, OR0647D - Extremity - Childrens Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

The Stryker Visum¿ LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures with high intensity light. Affected part numbers are 0682001432 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P/FP), 0682001286 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P/FP), 0682001298 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P), 0682001299 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P/5P), 0682001300 (EDS LIGHT SUSPENSION, CENTRAL AXIS, FP/5P/5P), 0682001433 (EDS LIGHT SUSPENSION, CENTRAL AXIS,

Stryker Communications

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800415002, Sterile, OR0484B- Shoulder System Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800599001, Sterile, GS0694A - Robotic Lap - Christus Highland

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

UOC Femoral Driver, Product number PE 93045101, orthopedic manual surgical instrument/accessory for use during surgery to implant femoral components and femoral trial, and to remove femoral trial.

United Orthopedic Corporation

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800553001, Sterile, OR0642A - Total Knee - Medical Center Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800553003, Sterile, OR0642C - Total Knee - Medical Center Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800411003, Sterile, NU0480C- Neuro PK - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800623001, Sterile, NU0787A - Neuro - Medical Center Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800599001, Sterile, GS0694A - Robotic Lap - Christus Highland

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880330004, Sterile, OR0761D - Total Hip - OSU

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800599003, Sterile, GS0694C - Robotic Lap - Christus Highland

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880331002, Sterile, OR0762B - Total Knee - OSU

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800528004, Sterile, GS0612D - Lap Chole Pk - Westover Hills

Resource Optimization & Innovation Llc

FDA Devices Critical Apr 5, 2017

7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070, K15-00170, PSS-7F-4-035MT, PSS-7F-4MT. Produc Usage: The Merit Prelude¿ Short Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries while maintaining hemostasis for a variety of diagnostic and therapeutic procedures. The device can also provide access to a native or synthetic graft used for hemodialysis. The side port of the sheath allows adequ

Merit Medical Systems, Inc.

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800401002, Sterile, GS0470B - Lap PK - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800559003, Sterile, ET0648C - Head & Neck - Childrens Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800430004, Sterile, LD0499D - C Section Pk - Cabrini

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880327009, Sterile, CV0758I - Open Heart A&B - OSU

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800557002, Sterile, LD0646B - C Section - Childrens Santa Rosa

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800418002, Sterile, GY0487B - Major Vaginal Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800091003, Sterile, LD0692C - C Section - FMOL Lady of Angels

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Cyto-Chex BCT - blood specimen collection device - Immunophenotyping Preservative. IVD. Sterile. 2.0ml only. Packaged 6-tube pack REF 213559 and 100-tube box REF 218980. Streck.

Streck

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800407003, Sterile, OR0476C - Ortho Pk - Spohn

Resource Optimization & Innovation Llc

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880327008, Sterile, CV0758H - Open Heart A&B - OSU

Resource Optimization & Innovation 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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2017

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 2017 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.