PlainRecalls

2017 Recalls

7,480 recalls · Page 150 of 150

2017 Recall Year Insight

Federal agencies issued 7,480 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 8.91% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.5 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 150 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 30 records, severity classification shows 2 critical, 21 moderate, and 7 lower-severity recalls. The page references 11 distinct recalling firms operating in 5 distinct product categories, with 28 of 30 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), CPSC (3), NHTSA (2), 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 Moderate Jan 4, 2017

SOMATOM Perspective, Computed tomography x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jan 4, 2017

ADVANTX LCV+

GE Healthcare, LLC

FDA Devices Moderate Jan 4, 2017

Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is intended for use as a data pr…

PerkinElmer Health Sciences, Inc.

FDA Devices Moderate Jan 4, 2017

NeuViz 64 Multi-slice CT Scanner Systems

Neusoft Medical Systems Co., Ltd.

FDA Devices Moderate Jan 4, 2017

Prestilix

GE Healthcare, LLC

FDA Devices Moderate Jan 4, 2017

Innova 2000

GE Healthcare, LLC

FDA Devices Moderate Jan 4, 2017

Legacy

GE Healthcare, LLC

FDA Devices Moderate Jan 4, 2017

Shimadzu X-ray High Voltage Generator Model No. UD150B-40 on SONIALVISION safire II/17 systems with 0.7/1.2JG326D X-Ray Tube Diagnostic x-ray high…

Shimadzu Medical Systems

FDA Devices Moderate Jan 4, 2017

NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.

Medtronic Xomed, Inc.

FDA Devices Low Jan 4, 2017

Enzymatic Cholesterol (Trinder/COD-CEH) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer…

Sterling Diagnostics, Inc.

FDA Devices Low Jan 4, 2017

Sterling Diagnostics, Inc., Enzymatic Uric Acid (Uricase Trinder) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These ar…

Sterling Diagnostics, Inc.

FDA Devices Low Jan 4, 2017

Sterling Diagnostics, Inc., Enzymatic Glucose for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a c…

Sterling Diagnostics, Inc.

FDA Devices Moderate Jan 4, 2017

ADVANTX LCLP+

GE Healthcare, LLC

FDA Devices Low Jan 4, 2017

Sterling Diagnostics, Inc., HDL Cholesterol (PEF Method) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMA…

Sterling Diagnostics, Inc.

FDA Devices Moderate Jan 4, 2017

ADVANTX LCN+

GE Healthcare, LLC

FDA Devices Moderate Jan 4, 2017

SFX

GE Healthcare, LLC

FDA Devices Moderate Jan 4, 2017

Shimadzu X-ray TV System, Catalog No. SONIALVISION G4

Shimadzu Medical Systems

FDA Devices Moderate Jan 4, 2017

NeuViz 128 Multi-slice CT Scanner System with software version 1.0.7.4038+P06 or previous version

Neusoft Medical Systems Co., Ltd.

FDA Devices Moderate Jan 4, 2017

SOMATOM Scope Power, Computed tomography x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Low Jan 4, 2017

Sterling Diagnostics, Inc., SGPT Colorimetric for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a cu…

Sterling Diagnostics, Inc.

FDA Devices Low Jan 4, 2017

Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a cu…

Sterling Diagnostics, Inc.

FDA Devices Moderate Jan 4, 2017

SOMATOM Scope, Computed tomography x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Low Jan 4, 2017

Sterling Diagnostics, Inc. Serum Iron/IBC (Colorimetric) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMA…

Sterling Diagnostics, Inc.

FDA Devices Moderate Jan 4, 2017

VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Produ…

ORTHO-CLINICAL DIAGNOSTICS

FDA Devices Moderate Jan 4, 2017

Prestige II

GE Healthcare, LLC

CPSC Moderate Jan 4, 2017

Curio Design Recalls Modular Lights and Bases Due to Shock and Fire Hazards (Recall Alert)

Curio Design Inc., of Culver City, Calif.

CPSC Moderate Jan 4, 2017

Toshiba Expands Recall of Laptop Computer Battery Packs Due to Burn and Fire Hazards

Panasonic, of Japan

CPSC Moderate Jan 4, 2017

Walt Disney Parks and Resorts Recalls Minnie and Mickey Mouse Infant Hoodie Sweatshirts Due to Choking Hazard

NHTSA Critical Jan 3, 2017

AUDI 2012-2017: ENGINE AND ENGINE COOLING:COOLING SYSTEM

AUDI

NHTSA Critical Jan 3, 2017

AUDI 2011-2017: VISIBILITY:SUN/MOON ROOF ASSEMBLY

AUDI

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