PlainRecalls

2017 Recalls

7,536 recalls · Page 62 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 8 critical, 40 moderate, and 2 lower-severity recalls. The page references 26 distinct recalling firms operating in 4 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (38), FDA Drug (12), 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 Drug Critical Jul 19, 2017

UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules, supplied in 2, 4 and 10 count packages, Distributed by AH Distribution, DelR…

Organic Herbal Supply

FDA Drug Moderate Jul 19, 2017

Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total Approximate Volume 255 mL, Rx only, SCA Pharmaceuticals, Little R…

SCA Pharmaceuticals

FDA Drug Critical Jul 19, 2017

EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and Pfizer Inc. New York, NY 10017 U…

Bristol-myers Squibb Company

FDA Drug Critical Jul 19, 2017

ZRECT Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic …

Organic Herbal Supply

FDA Drug Critical Jul 19, 2017

TORNADO Male Enhancement Herbal Dietary Supplement Capsules, Over 4000 mg value, supplied in 2, 4 and 10 count packages, Made in USA Distributed b…

Organic Herbal Supply

FDA Drug Moderate Jul 19, 2017

Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 15 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-…

Advanced Pharma Inc.

FDA Drug Moderate Jul 19, 2017

Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 30 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-…

Advanced Pharma Inc.

FDA Drug Low Jul 19, 2017

Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202,…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Jul 19, 2017

Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 10 mMol (14.67 mEq K+) Total Approximate Volume 254 mL, Rx only, SCA Pharmaceuticals, Little…

SCA Pharmaceuticals

FDA Drug Critical Jul 19, 2017

ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UP…

Organic Herbal Supply

FDA Drug Critical Jul 19, 2017

BRILINTA (ticagrelor) tablets, 90 mg, 8-count Professional Sample bottles, Rx only, Mfd. for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850; …

AstraZeneca Pharmaceuticals, LP

FDA Drug Critical Jul 19, 2017

BIGnHARD Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Orga…

Organic Herbal Supply

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

FDA Devices Moderate Jul 19, 2017

Infinity 7, Implantable Pulse Generator, REF 6663, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be con…

St. Jude Medical, Inc.

FDA Devices Moderate Jul 19, 2017

10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange, Red, Blue, Purple, Yellow Rings), Check Valve, 0.2 Micron Filter, Clamp, Rotating Luer. …

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

Infinity 5, Implantable Pulse Generator, REF 6660, Rx only, STERILE EO, Product Usage: The Infinity IPG is an electronic device designed to be c…

St. Jude Medical, Inc.

FDA Devices Moderate Jul 19, 2017

Leksell Gamma Knife Icon is a teletherapy device intended for stereotactic irradiation of head structures ranging from very small target sizes of a f…

Elekta, Inc.

FDA Devices Moderate Jul 19, 2017

Infinity 7, Implantable Pulse Generator, REF 6662, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be con…

St. Jude Medical, Inc.

FDA Devices Moderate Jul 19, 2017

Arrow EVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology

Arrow International Inc

FDA Devices Moderate Jul 19, 2017

Proclaim 7 Elite, Implantable Pulse Generator, REF 3662, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an …

St. Jude Medical, Inc.

FDA Devices Moderate Jul 19, 2017

The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM), a major component of the Merge Hemo software.

Merge Healthcare, Inc.

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

FDA Devices Moderate Jul 19, 2017

On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valve…

CryoLife, Inc.

FDA Devices Moderate Jul 19, 2017

XARIO 200 TUS-X200 diagnostic ultrasound system

Toshiba American Medical Systems Inc

FDA Devices Moderate Jul 19, 2017

Infinity 5, Implantable Pulse Generator, REF 6661, Rx only, STERILE EO Product Usage: The Infinity IPG is an electronic device designed to be con…

St. Jude Medical, Inc.

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

FDA Devices Moderate Jul 19, 2017

APLIO 500 TUS-A500 diagnostic ultrasound system

Toshiba American Medical Systems Inc

FDA Devices Critical Jul 19, 2017

ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI Disposable Series. Model c…

Oscor, Inc.

FDA Devices Low Jul 19, 2017

Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calib…

AMS Diagnostics, LLC

FDA Devices Moderate Jul 19, 2017

10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, Clamp, Rotating Luer. Product Usage: The device is a single use, sterile, non-py…

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

Alaris Pump Module model 8100

CareFusion 303, Inc.

FDA Devices Moderate Jul 19, 2017

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

GE Healthcare, LLC

FDA Devices Moderate Jul 19, 2017

The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of respiratory therapy and anesthes…

Natus Medical Incorporated

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

FDA Devices Moderate Jul 19, 2017

Arrow Glide Thru Peel-Away Sheath/Dilator Introducer

Arrow International Inc

FDA Devices Moderate Jul 19, 2017

Nicolet¿ Elite¿ 3 MHz OB Probe, Model #: X1L001, Catalog Code: N300. Intended for non-invasive support, i.e. early detection of fetal life, monito…

Natus Neurology Inc

FDA Devices Moderate Jul 19, 2017

Proclaim 5 Elite, implantable Pulse Generator, REF 3660, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an …

St. Jude Medical, Inc.

FDA Devices Moderate Jul 19, 2017

Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl, Urea N, Urea, Glucose Cre…

Beckman Coulter Inc

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

FDA Devices Moderate Jul 19, 2017

168 cm (66") Appx 2.6 ml, PVC/PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, MicroClave¿ Clear, Rotating Luer. Product Usage: …

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

VIDAS Testosterone, Ref 30418

bioMerieux, Inc.

FDA Devices Moderate Jul 19, 2017

28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, 2 NanoClave¿, Rotating Luer. Product Usage: The device is a single use,…

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

FDA Devices Moderate Jul 19, 2017

O-Two Adult Ventilation Timer, MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 --- INTENDED USE: The Adult Ven…

O-Two Medical Technologies, Inc.

FDA Devices Moderate Jul 19, 2017

Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and therapeutic access to, the biliar…

Pentax of America Inc

FDA Devices Moderate Jul 19, 2017

Exactech Optetrak Logic CC 15mm Tibial Augment Screws

Exactech, Inc.

FDA Devices Moderate Jul 19, 2017

Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripheral org…

Fujifilm Medical Systems U.S.A., Inc.

FDA Devices Moderate Jul 19, 2017

Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive support, i.e. early detection of…

Natus Neurology Inc

FDA Devices Moderate Jul 19, 2017

28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage: The device is a single use…

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of…

ICU

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.