PlainRecalls

2017 Recalls

7,536 recalls · Page 58 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 4 critical, 40 moderate, and 6 lower-severity recalls. The page references 23 distinct recalling firms operating in 7 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (20), FDA Drug (19), CPSC (6), 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 Food Moderate Jul 26, 2017

B10065, FINE CRAX MEAL, NET WT 50 LBS, Manufactured By: Newly Weds Foods, Inc., Chicago, IL 60639

Newly Weds Foods Inc

FDA Food Moderate Jul 26, 2017

A84249, BATTER MIX X1, NET WT 50 LBS, Manufactured By: Newly Weds Foods, Inc., Chicago, IL 60639

Newly Weds Foods Inc

FDA Drug Low Jul 26, 2017

PONSTEL (Mefanamic Acid) USP, 250 mg capsules, 30-count bottles, Rx Only, Manufactured for: Shionogi Inc. Florham Park, NJ 07932 Manufactured by: Hal…

Shionogi Inc.

FDA Drug Moderate Jul 26, 2017

Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV Use, PharMedium Services, LLC…

PharMedium Services, Llc

FDA Drug Low Jul 26, 2017

Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma Limited, Hyderabad, India, Ma…

Hospira Inc., A Pfizer Company

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection, 7 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Bl…

PharMedium Services, Llc

FDA Drug Low Jul 26, 2017

Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wale…

Teva Pharmaceuticals USA

FDA Drug Low Jul 26, 2017

Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Halo…

Shionogi Inc.

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection, 9 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Bl…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection, 10 mMol in a) 100 mL in 150 mL Intravia Bag (NDC 61553-288-48) Service Code: 2K5288, and b) 25…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 5% Dextrose Injection, 7.5 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection, 40 mMol in 250 mL in 250 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport B…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 5% Dextrose Injection, 9 mMol in 50 mL in 50 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sug…

PharMedium Services, Llc

FDA Drug Low Jul 26, 2017

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per Bottle, Rx only, Distributed By: Teva Pharmaceuticals USA, Inc., North Wales, …

Teva Pharmaceuticals USA

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 5% Dextrose Injection, 15 mMol in 250 mL in 250 mL Intravia Bag Service, Rx Only. PharMEDium Services, LLC 12620 W. Airport Bl…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in a) 100 mL in 150 mL Intravia Bag Service Code 2K5295 NDC# 61553-295-48; b) 150 mL in…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection, 7.5 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport …

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection, 30 mMol in a) 250 mL in 250 mL Intravia Bag Service Code 2K5290 NDC# 61553-290-11, b) 500 mL i…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 5% Dextrose Injection, 30 mMol 500 mL in 500 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sug…

PharMedium Services, Llc

FDA Drug Moderate Jul 26, 2017

Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Bl…

PharMedium Services, Llc

FDA Drug Low Jul 26, 2017

Obagi-C Rx System C-Therapy Night Cream, Net wt. 2 oz. (57g) bottle, Rx only, Distributed by OMP, Inc., Long Beach, CA Made in USA, NDC 62032-222-02

Valeant Pharmaceuticals North America LLC

FDA Devices Moderate Jul 26, 2017

9400 Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of laryngeal o…

Pentax of America Inc

FDA Devices Moderate Jul 26, 2017

9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data of …

Pentax of America Inc

FDA Devices Moderate Jul 26, 2017

Install CD, Spine tools, Plus and S7, Version 25. Model Number 9731958.

Medtronic Navigation, Inc.

FDA Devices Critical Jul 26, 2017

Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic stroke secondary to intracran…

Penumbra Inc.

FDA Devices Moderate Jul 26, 2017

BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for genera…

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

Standex International Bakers Pride Microwave Ovens Model E300

Standex Intl Corp

FDA Devices Moderate Jul 26, 2017

MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries duri…

Mako Surgical Corporation

FDA Devices Moderate Jul 26, 2017

Merge Eye Care PACS Viewer 5.2 Merge Eye Care PACS is a software solution for the display, management, archive, interface and integration of ophthal…

Merge Healthcare, Inc.

FDA Devices Moderate Jul 26, 2017

PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. Manufactured by: Flowonix Medi…

Flowonix Medical, Inc.

FDA Devices Moderate Jul 26, 2017

BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #305062

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

Agfa Healthcare NX 3.0.8950 Imaging Processing Software

AGFA Healthcare Corp.

FDA Devices Moderate Jul 26, 2017

BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purp…

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

7245C, 7245C/E, 7245D Computer Digital Video System Product Usage: The 7245C, 7245C/E and 7245D are used to electronically record, display, tran…

Pentax of America Inc

FDA Devices Moderate Jul 26, 2017

Draeger Medical Systems Infinity Acute Care System (M540) Catalog Numbers: MK31501/MK31701/MK31722

Draegar Medical Systems, Inc.

FDA Devices Moderate Jul 26, 2017

Artis zee,x-ray system, angiographic Artis zee is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and …

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 26, 2017

BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #309580 The BD Single Use, Hypodermic Syringe is int…

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general pur…

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration of fluid…

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G x 1 (0.6mm x 25mm) Catalog #309571 The BD Single Use, Hypodermic Syringe is intende…

Becton Dickinson & Company

FDA Devices Moderate Jul 26, 2017

9310HD Digital Video Capture Modules Product Usage: The 9310HD is used to electronically record, display, transfer, and store digital video data…

Pentax of America Inc

NHTSA Critical Jul 26, 2017

MAZDA 2003-2008: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

MAZDA

CPSC Moderate Jul 25, 2017

Outxpro Mosquito Zapper LED Light Bulbs Recalled by R & D Products Due to Shock Hazard; Sold Exclusively at Amazon.com (Recall Alert)

CPSC Moderate Jul 25, 2017

Polaris Recalls RZR 170 Recreational Off-Highway Vehicles Due to Fuel Leak, Fire Hazards

Aeon Motors Ltd., of Taiwan

CPSC Moderate Jul 25, 2017

Quality Foam Recalls Mattresses Due to Violation of Federal Mattress Flammability Standard

Quality Foam, of Brooklyn, New York

NHTSA Critical Jul 25, 2017

FORD,LINCOLN 2014-2015: SEAT BELTS

FORD,LINCOLN

NHTSA Critical Jul 25, 2017

KENWORTH,PETERBILT 2013-2017: EXTERIOR LIGHTING

KENWORTH,PETERBILT

CPSC Moderate Jul 24, 2017

iRover Recalls Self-Balancing Scooters/Hoverboards Due to Fire Hazard

CPSC Moderate Jul 21, 2017

ZORJAR Recalls Women's Scarves Due to Violation of Federal Flammability Standard; Sold Exclusively on Amazon.com (Recall Alert)

Zhe Jiang Yin Suo Zhi Ran You Xian Gong Si, of China

CPSC Moderate Jul 20, 2017

Manhattan Toy Recalls Activity Toys Due to Choking Hazard

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 July 2026.