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 0 critical, 48 moderate, and 2 lower-severity recalls. The page references 23 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), FDA Drug (3), 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 Drug Moderate Apr 19, 2017

ESTRONE, USP Bulk, in a) 100 mgs (NDC 38779-0891-05), b) 1 gram (NDC 38779-0891-06), c) 5 grams (NDC 38779-0891-03), d) 25 grams (NDC 38779-0891-04), and e) 100 grams (NDC 38779-0891-09) Bottles, Packed by MEDISCA INC. PLATTSBURGH, NY 12901; Product Code 0891

Medisca, Inc.

FDA Drug Low Apr 19, 2017

Fluocinolone Acetonide Topical Solution USP 0.01% For Topical Use Only, Not for Ophthalmic Use, 60 mL bottle, Rx Only, Manufactured for Gavis Pharmaceuticals, LLC, Somerset NJ 08873, Manufactured by Novel Laboratories, Inc. Somerset, NJ 08873, NDC 43386-069-60

Novel Laboratories, Inc.

FDA Drug Low Apr 19, 2017

Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.

Allergan Sales, LLC

FDA Devices Moderate Apr 19, 2017

Merge Hemo software. The firm name on the labeling is Merge Healthcare, Hartland, WI. Merge Hemo monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure

Merge Healthcare, Inc.

FDA Devices Moderate Apr 19, 2017

CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.

Smiths Medical ASD Inc.

FDA Devices Moderate Apr 19, 2017

Cataract Pack, part numbers 008886-1, AMS2806, PSS3442, PSS3442(A, WAL1155, and WAL1155(A. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

HYFRECATOR 2000 HANDPIECE SHEATH, REF/Part Number 7-796-19, Rx ONLY, STERILE, Single Patient Use -- CONMED CORPORATION, 525 FRENCH ROAD UTICA, NY 13502. --- There is no problem with the Hyfrecator 2000 Electrosurgical Units or with cases of P/N 7-796-19 sold in cases as P/N 7-796-19BX or P/N 7-796-19CS.

ConMed Corporation

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. General and Plastic Surgery: The EndoWrist¿ Suction Irrigator is designed to be used in conjunction with an Intuitive Surgical da Vinci Surgical System and compatible suction and irrigation sources and tubing sets for delivering fluid to the surgical site and for evacuation and aspiration of fluids. The instrument may also be used for retraction and blun

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 use only. They may be sold sterile, non-sterile, and bulk packed. Custom tubing sets that are sold sterile are not to be re-sterilized by the user. In open heart surgery the HLM Tubing Sets with Bioline Coating are used in combination with the heart-lung machine for the oxygenation of blood and removal of carbon dioxide. The main purpose of the HLM

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 within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.

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 VOLTS AC, REF/Catalog Number 7-900-230, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Units. -- ASSEMBLED IN MEXICO -- CONMED CORPORATION 525 FRENCH ROAD UTICA, NY 13502

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 neurosurgeons to guide standard neurosurgical instruments during spine surgery. Guidance is based on an intra-operative plan developed with three dimensional imaging software provided that the required fiducial markers and rigid patient anatomy can be identified on 3D CT scans. The device is indicated for the placement of pedicle screws in lumbar vertebr

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 VOLTS AC, REF/Catalog Number 7-900-220, Rx Only, There is no problem with the Hyfrecator 2000 Electrosurgical Units --- ASSEMBLED IN MEXICO -- CONMED CORPORATION 525 FRENCH ROAD UTICA, NY 13502 ---

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-621RA) and CNS-9701A (MU-971RA).

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 Road, Skaneateles Falls, NY 13153 --- Microlife Corporation 9F, 431, RuiGuang Road, NeiHu, Taipei, 11492, Taiwan, R.O.C. --- Microlife AG Espenstrasse 139 9443 Widnau, Switzerland

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 radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose distributions expected during the proposed treatment, and may be used to administer treatments after review and approval by the intended user. The system functionality can be configured based on user needs

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 VOLTS AC, REF/Catalog Number 7-900-100, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Unit. -- ASSEMBLED IN MEXICO --- CONMED CORPORATION 525 FRENCH ROAD UTICA, NY 13502

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 radial and ulnar artery following catheterization procedures. It has a soft wristband with a secure hook and loop fastener. The band delivers adjustable compression of the puncture site with an inflatable bulb, and a check valve for easy inflation and deflation with a syringe. A clear curved backer plate provides optimal visualization of the puncture

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 devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses, and Technicians, who will determine when use of the device is indicated, based upon their professional assessment of the patients medical condition. The Infinity Delta Series (Delta/Delta XL/Kappa) monitors are intended

Draegar Medical Systems, 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: 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.