PlainRecalls

2017 Recalls

7,536 recalls · Page 101 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 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 22 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, 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 19, 2017

Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Dicken Eye Pack, part number CPA-3202-2. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

da Vinci Xi EndoWrist Suction Irrigator, 8 mm instrument; PN 480299-03; and SOFTWARE, EMBEDDED RLS, IS4000, A70_P6_B440; PN 610092-440. Gener…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 19, 2017

Custom Tubing Pack with Bioline Coating UDI code: 00607567208230 Part Number: 709000058 The HLM Tubing Sets with Bioline Coating are for single …

Datascope Corporation

FDA Devices Moderate Apr 19, 2017

VITROS Immunodiagnostic Products NT-pro BNP Reagent Pack, REF/Catalog 680 2156, IVD --- Ortho-Clinical Diagnostics Pencoed, Bridgend CF35 5PZ, UK

ORTHO-CLINICAL DIAGNOSTICS

FDA Devices Moderate Apr 19, 2017

Volt Resistance Frostie Heated Gloves (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

iConnect Enterprise Archive (ICEA) software. The firm name on the labeling is Merge Healthcare, Hartland, WI.

Merge Healthcare, Inc.

FDA Devices Moderate Apr 19, 2017

AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures withi…

Aesculap Implant Systems LLC

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 230 …

ConMed Corporation

FDA Devices Moderate Apr 19, 2017

MEDTECH ROSA Spine 1.0.2 The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neuro…

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

PRK Tray, part number DDS1044 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Vitrectomy Kit, part number CMP1016(A. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Ophthalmic Pack, Part number WAL1107(A and WAL1190 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Cobas 8100 bi-directional reformatter (BRF) module with Software Version 02-xx

Roche Diagnostics Corporation

FDA Devices Moderate Apr 19, 2017

Vivid S60/S70/S60N/S70N, H45041SU, H45041SW, H45581MS, H45581PD.

GE Healthcare, LLC

FDA Devices Moderate Apr 19, 2017

Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons , 220…

ConMed Corporation

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The Problem only affects CSM-1901(Life Scope G9) communicating with CNS-6201A (PU-…

Nihon Kohden America Inc

FDA Devices Moderate Apr 19, 2017

Vivid E95/E90/E80, H45581DC, H45581LB and H45581DA.

GE Healthcare, LLC

FDA Devices Moderate Apr 19, 2017

Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Boston Scientific Imager II Angiographic Catheter, M001316581 (5-pack outer package UPN), M001316580, single unit, inner package UPN)

Boston Scientific Corporation

FDA Devices Moderate Apr 19, 2017

Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch Allyn Inc., 4341 State Street…

Welch Allyn Inc

FDA Devices Moderate Apr 19, 2017

Setup Pack, part number AMS3112(A Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

ENT Pack, part number AMS2727 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Cataract Kit - Dr. Slingsby, part number CMP1017(B. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment planning and analysis of rad…

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Apr 19, 2017

Nordson Micromedics FibriJet Endoscopic Catheter Introducer, Catalog Number SA-3445. Sterilized using Ethylene Oxide

Micromedics, Inc.

FDA Devices Moderate Apr 19, 2017

Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 100 …

ConMed Corporation

FDA Devices Moderate Apr 19, 2017

The PreludeSYNC Radial Compression Device is a sterile, single use disposable device used to assist in gaining and maintaining hemostasis of the radi…

Merit Medical Systems, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Minor Operation Kit, part number AMS1530 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Delta, Catalog Number: MS18597 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The device…

Draegar Medical Systems, Inc.

FDA Devices Moderate Apr 19, 2017

Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 115 …

ConMed Corporation

FDA Devices Moderate Apr 19, 2017

Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and…

Ge Medical Systems Information T

FDA Devices Moderate Apr 19, 2017

Delta XL, Catalog Number: MS18596 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The devi…

Draegar Medical Systems, Inc.

FDA Devices Moderate Apr 19, 2017

Cobas 8100 uni-directional reformatter (BRF) module with Software Version 02-xx

Roche Diagnostics Corporation

FDA Devices Moderate Apr 19, 2017

Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K

Keystone Dental Inc

FDA Devices Moderate Apr 19, 2017

Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

TotalCare Bed Systems, Model Numbers P1900, PR1900, and U1900 with 3-Level Patient Position Monitoring and Scale Upgrade Kits, Model Numbers P1947A …

Hill-Rom, Inc.

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.